Method for synthesizing cDNA from mRNA sample

Abstract

cDNA including the 5′-terminal sequence of full-length mRNA with a cap structure is synthesized from a mRNA sample containing the full-length mRNA with the cap structure and non-full-length mRNA without any cap structure in mixture. At the first step, the phosphate group at 5′-terminus of the non-full-length mRNA in the mRNA sample is removed. At the second step, the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample is removed. At the third step, an oligoribonucleotide is ligated to the phosphate group at 5′-terminus of mRNA generated through the first and second steps. At the fourth step, mRNA with the oligoribonucleotide ligated at the 5′-terminus thereof at the third step is subjected to a reverse transcriptase process using a short-chain oligonucleotide capable of being annealed to an intermediate sequence within the mRNA as primer, to synthesize a first-strand cDNA.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to a method for synthesizing cDNA from a mRNA sample and to tobacco acid pyrophosphatase for use in the method; more specifically, the invention relates to a rapid synthesis method of cDNA including the 5′-terminal region of mRNA in a sample for the analysis of a nucleotide sequence derived from the 5′-terminus of the mRNA.

2. Background of the Invention

Numerous types of proteins composing cell are present, such as proteins involved in cell morphology, proteins involved in development or proteins involved in metabolism. The patterns of the presence undoubtedly determine the properties of cell. Essential information relating to the mode of these presence and functions is imprinted in the gene in cell and is realized by mRNA as a copy of the gene. mRNA functions as template for protein translation and also as a carrier of the information flow from DNA to protein. Ultimately, mRNA reflects the “phenotypes” in all biological organisms. These proteins are industrially valuable and possibly applicable as pharmaceutical drugs, diagnostic agents, bio-sensors and bio-reactors, provided that these proteins are biologically active substances. Hence, it is very important to recover full-length mRNA and procure gene information from the mRNA. Recent progress in the gene recombinant technology and more recent promotion in the genome analysis project are now permitting cDNA cloning and analysis technology readily usable.

Although rapid analysis of complete 5″-terminal sequence of mRNA has increasingly been demanded in recent years, no technology has been established yet to enable such rapid analysis in a simple and rapid fashion. Because the 5′-terminal sequence of full-length mRNA contains a transcription start for gene expression analysis on genome, rapid analysis of the 5′-terminal sequence as well as enormous quantities of sequenced genome open up a way for transcription gene mapping. Furthermore, accurate information of the 5′-terminal sequence of mRNA can identify the sequences of gene expression regulatory promoters present upstream. These promoters are cis-factors regulating when, where and how much a gene should be expressed. The detection of the 5′-terminal sequence of mRNA verifies that an upstream promoter sequence is functional, which suggests a new possibility for the etiological analysis or diagnosis or therapeutic treatment of diseases.

Practically, the information as to when, where and how much a gene is expressed is very valuable information for the etiological analysis or diagnosis or therapeutic treatment of diseases. The Human Genome Project currently promoted internationally mentions as one of the goals to collect such information. The ultimate purpose of the Project lies in the nucleotide sequencing of biological genome. The nucleotide sequences of several bacterial genome species and the nucleotide sequences in the whole genome of budding yeast have already been sequenced and reported. Most of many genes identified on the isolated genome species are functionally not yet identified, which is a big issue in future. In that sense, the significance of the analysis of cDNA reflecting the gene expression dynamics in cell is increasingly drawing attention.

Herein, by the term cDNA referred to as complementary DNA is meant DNA synthetically prepared by reverse transcriptase using mRNA as template. In other words, the information of mRNA encoding the information of the amino acid sequence of protein is synthetically constructed as cDNA. The analysis of the cDNA can readily determine the primary structure of the protein and can readily promote the development of a large-scale expression system. Thus, such cDNA preparation is now very important, industrially.

Ideally, the ultimate goal of the cDNA cloning technology lies in the replacement of all expressed mRNAs with complete cDNAs. Thus, the information is greatly valuable. In other words, the information recovered from such full-length cDNA serves as a starting point for the analysis of the information on genome, because the information includes the information of transcription start and the entire information of expressed protein. The primary protein sequence recovered from a complete coding sequence distinctively shortens the time required for the functional analysis.

However, the technology for the recovery of cDNA including full-length mRNA has been a not-yet matured technology “still under way of development” among the DNA technologies in rapid progress. For example, the Gubler-Hoffman method (Gene, Vol. 25, pp. 236-269, 1983) is known as one of synthesis method of cDNAs commonly applied conventionally. Nevertheless, many of cDNAs synthesized by the method are incomplete with terminal deficiency. Alternatively, the Okayama-Berg method (Mol. Cell. Biol., Vol. 2, pp. 161-170, 1982) is a synthesis method characteristic in that full-length cDNA is readily prepared. Even by the method, however, reverse transcription sometimes stops in the course of cDNA synthesis, so no guarantee is given to the resulting cDNA that it is of full length.

The RACE method (Rapid amplification of cDNA ends: Proc. Natl. Aca. Sci. USA, Vol. 85, pp. 8998-9002, 1988) has been suggested as a method to supplement a portion lacking in cDNA, based on the partial cDNA sequences recovered by the existing methods, so as to acquire the complete information of mRNA. The method comprises reverse transcription based on a target cDNA sequence to add a homopolymer to both the ends of cDNA by terminal transferase or to ligate an adapter comprising a synthesized DNA to both the ends of cDNA by T4 DNA ligase, and polymerase chain reaction (PCR) based on these added sequences and a primer specific to the target cDNA, thereby analyzing only the terminal regions of mRNA sequence.

The analysis of the target 5′-terminus of mRNA in particular by the method (referred to as 5′-RACE) can be done in a very simple fashion, because PCR is utilized by the method. Accordingly, the method is frequently used. Principally, however, the method apparently cannot analyze the 5′-terminal sequence of mRNA used for the preparation of the cDNA, although the method can analyze the 5′-terminus of cDNA. Hence, the recovery of complete 5′-terminus of mRNA is very difficult, compared with the recovery of complete 3′-terminus by 3′-RACE, in which poly-A sequence is responsible for the protection role against terminal deficiency. As described above, even currently, the method is acclaimed as a “not-yet established technology”.

It is known that the 5′-terminus of complete mRNA has a characteristic structure called cap structure (Nature, Vol. 253, pp. 374-375, 1975). An attempt has been suggested to analyze cDNA, targeting the vicinity of the cap structure (Japanese Patent Laid-open No. 6-153953 (1994); Gene, Vol. 138, pp. 171-174, 1994).

According to these methods, tobacco acid pyrophosphatase (referred to as “TAP” hereinafter) specifically cleaving the cap structure is used. These methods comprise treating mRNA with alkali phosphatase to remove the phosphate group from the 5′-terminus of mRNA without any cap, subsequently treating the resulting mRNA with TAP to cleave the cap, adding an oligoribonucleotide and continuously effecting reverse transcription, to synthesize cDNA. Although these methods are complicated because enzymatic reactions continue over plural steps, these methods are a few effective methods principally capable of specifically analyzing full-length mRNA. Nevertheless, these methods include problems to be improved in the steps. Currently, therefore, these methods are not commonly widespread, although these methods are greatly needed due to the significance of the 5′-terminal sequencing as described above.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide a synthesis method of cDNA from mRNA, so as to recover the complete 5′-terminal sequence of cDNA at a large-scale in a rapid manner by selectively synthesizing cDNA including the 5′-terminal sequence of full-length mRNA with the cap structure. It is another object of the present invention to provide tobacco acid pyrophosphatase preferable for use in the synthesis method.

The present invention proposes to attain the above-mentioned objective by suggesting a DNA synthesis method for synthesizing cDNA including the 5′-terminal sequence of full-length mRNA with a cap structure from a mRNA sample containing the full-length mRNA with the cap structure and non-full-length mRNA without any cap structure in mixture, said method comprising:

a first step of removing the phosphate group at the 5′-terminus of the non-full-length mRNA in the mRNA sample;

a second step of removing the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample;

a third step of ligating an oligonucleotide of a predetermined sequence to the phosphate group at the 5′-terminus of the mRNA generated through the first and second steps in the sample; and

a fourth step of subjecting the mRNA ligated with the oligonucleotide at the phosphate group at the 5′-terminus to a reverse transcriptase process using as primer a short-chain oligonucleotide capable of being annealed to an intermediate sequence within the mRNA, to synthesize a first-strand cDNA;

characterized in that said oligoribonucleotide for use at the third step has a sequence recovered by preparing a number of oligoribonucleotide sequences including various combinations of bases in a predetermined number, carrying out a homology search with a predetermined nucleotide sequence data base to determine the occurrence number of a sequence completely matching or differing by one base, and preparing a combination of plural sequences in a low-frequency occurrence group including a sequence at the lowest occurrence number.

According to a preferred embodiment of the present invention, the third step comprises ligating an oligoribonucleotide of a predetermined sequence to the phosphate group.

According to another embodiment of the present invention, the third step comprises ligating an oligoribonucleotide composed of a sequence never contained in the sequence of the mRNA in the mRNA sample to the phosphate group.

Specifically, as the oligonucleotide, use is made of an oligoribonucleotide comprising a 10-base or longer sequence never contained in the sequence of the mRNA. More specifically, a great number of oligonucleotide sequences are prepared, the oligonucleotide sequences comprising various combinations of oligonucleotides of bases in a predetermined number; a homology search of each of the oligonucleotide sequences with a predetermined nucleotide sequence data base is then carried out; the occurrence number of a sequence completely matching or differing by one base is determined; by using combinations of plural sequences in the low occurrence frequency group including a sequence of the lowest occurrence frequency, a sequence is determined and an oligoribonucleotide of this sequence is used. In one embodiment of the invention, any one of the following oligoribonucleotides is used as such oligoribonucleotide.

5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAAGG-3′

5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′

5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′

5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′

5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′

5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGU-3′

5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGUAA-3′

According to still another embodiment of the present invention, the primer to be used at the fourth step is a short-chain oligonucleotide of a length of 6 bases or longer.

According to still another embodiment of the present invention, the cap structure at the 5-terminus of the full-length mRNA in the mRNA sample is removed by using tobacco acid pyrophosphatase purified to a high purity with no contamination of trace amounts of nuclease cleaving the phosphodiester bond comprising RNA and a phosphatase removing 5-phosphate group freshly generated after cap cleavage.

The present invention also proposes a method for synthesizing cDNA including the 5′-terminal sequence of full-length mRNA with a cap structure from a mRNA sample containing the full-length mRNA with the cap structure and non-full-length mRNA without any cap structure in mixture, the method comprising:

a first step of removing the phosphate group at the 5′-terminus of the non-full-length mRNA in the mRNA sample;

a second step of removing the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample by using tobacco acid pyrophosphatase highly purified by using alkali phosphatase;

a third step of ligating an oligoribonucleotide of a predetermined sequence to the phosphate group at the 5′-terminus of mRNA generated through the first and second steps in the sample, said oligoribonucleotide comprising a sequence never contained in the sequence of mRNA in the mRNA sample;

a fourth step of subjecting the mRNA ligated with the oligoribonucleotide at the phosphate group at the 5′-terminus to a reverse transcriptase process using as primer a short-chain oligonucleotide of 6 bases or more in length and with an ability being annealed to an intermediate sequence within the mRNA, to synthesize a first-strand cDNA; and

a fifth step of synthesizing a second-strand cDNA based on the resulting first-strand cDNA.

As the tobacco acid pyrophosphatase for use in the cDNA synthesis method of the present invention, it is preferable to use the tobacco acid pyrophosphatase which can remove the cap structure at the 5′-terminus and has already been purified at an extent such that the tobacco acid pyrophosphatase substantially never contains other enzymes cleaving the remaining sites within mRNA.

In accordance with the method of the present invention, only cDNA containing the 5′-terminal sequence of full-length mRNA with the cap structure is synthesized from a mRNA sample containing the full-length mRNA and non-full-length mRNA without the cap structure in mixture. Accordingly, it is preferable to preliminarily remove the phosphate group at the 5′-terminus of the non-full-length mRNA in the sample, thereby avoiding the occurrence of the additional reaction of oligonucleotide (preferably oligoribonucleotide) at the third step.

As to the full-length mRNA in the sample, it is preferable to remove the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample at the second step and then, in the third step, an oligonucleotide is ligated to the phosphate group thus generated at the fresh 5′-terminus of the mRNA. Prior to this reaction, the phosphate group at the 5′-terminus of the non-full-length mRNA is already removed. Thus, the additional reaction never progresses in the non-full-length mRNA.

As the oligonucleotide, use is preferably made of oligoribonucleotide, because the reaction efficiency of an enzyme T4 RNA ligase when used differs in the order of two digits between substrates RNA and DNA.

At the fourth step, subsequently, mRNA with the oligonucleotide ligated at the phosphate group at the 5′-terminus thereof is subjected to a reverse transcriptase process using as primer a short-chain oligonucleotide to be annealed to an intermediate sequence within the mRNA. Thus, a complementary first-strand cDNA is synthesized. In such manner, cDNA can be synthesized readily, starting from the 5′-terminus of mRNA.

Preferably, the fifth step is satisfactrrily added to synthesize a double-stranded cDNA from a single-stranded cDNA. The fifth step comprises additionally synthesizing a second-strand cDNA from the resulting first-strand cDNA.

One characteristic aspect of the present invention lies in the use as primer of a short-chain oligonudeotide (“random hexamer” of 6 bases, in particular, in accordance with the present invention) capable of being annealed to an intermediate sequence within mRNA, preferably a sequence in the vicinity of the 5′-terminus.

For more detailed description of the characteristic aspect, the present invention relates to a method for converting the information of mRNA to cDNA. General methods comprise synthesizing a complementary DNA using reverse transcriptase and RNA as template. Then, primer is needed for the initiation of the reaction with the reverse transcriptase. The term primer means DNA chain or RNA chain supplying nucleotide 3′-OH required by a template-dependent DNA polymerase for the synthesis of a new chain. Current progress of DNA synthesis technology enables ready synthesis of short-chain oligonucleotides of 15 to 40 bases in length and with a primer function.

For the purpose of cDNA synthesis, generally, use is made of oligo dT 12 18 primer complementary to a sequence of a series of plural adenines, as called poly-A chain, present on the 3′-terminus of mRNA. Although the synthesis efficiently starts in case that the primer is used, the synthesis rarely progresses up to the 5′-terminus of mRNA with the cap structure because of the instability and long chain of RNA and the secondary structure thereof, as described above. It is readily deduced that the tendency is likely more prominent in case that mRNA is longer. More additionally, the aforementioned grounds work to make full-length cDNA synthesis difficult. It cannot be said that any of the existing technologies attempting full-length cDNA synthesis can overcome the problem.

On the contrary, in accordance with the present invention, the 5′-terminal sequence of mRNA, in particular, can absolutely be analyzed rapidly, which has been considered difficult. One of the characteristic features of the present invention lies in the use as primer of a short-chain oligonucleotide capable of being annealed to an intermediate sequence within mRNA, preferably a sequence in the vicinity of the 5′-terminus. Particularly preferably, a short-chain oligonucleotide comprising a random sequence of 6 bases or more.

Theoretically, herein, the base length of the short-chain oligonucleotide used as the primer is an appropriate length shorter than the sequence of mRNA, in which reverse transcription can start from various sites of mRNA. It is currently reported that the shortest length required for sequence-specific primer activity is a length of 6 bases. Thus, the single-stranded oligonucleotide is of a length of 6 bases or longer in accordance with the invention.

In case that the shortest random hexamer comprising 6 bases is used as primer, principally, single-stranded oligonucleotides of 4096 (=4 6 ) nucleotide sequences are nominated as candidates. Among such numerous sequences, accordingly, a single-stranded oligonucleotide of a nucleotide sequence capable of initiating reverse transcription in a desired site of mRNA is satisfactorily selected. When such random hexamer is selected, the possibility of the synthesis of cDNA including the 5′-terminus of mRNA can be raised.

A reverse transcription method using a short-chain oligonucleotide of such appropriate nucleotide sequence is frequently utilized as the search method of clones along 5′-direction, for the cloning of cDNA derived from large mRNA. The method is described in for example J. Virol., Vil. 28, p. 743 (1978).

However, the procedure described in the method in J. Viol. and the procedure of the method according to the present invention are identical in terms of reverse transcription by means of short-chain oligonucleotide but are totally different in that only 5′ cDNA is selectively amplified by the procedure according to the present invention. Because the method described in J. Virol. comprises reverse transcription, and subsequent synthesis of a second strand and integration thereof in a vector, clones where reverse transcription has never progressed up to 5′-terminus are generated; and furthermore, generally, a linker DNA is attached for the insertion into a vector. During the course of the attachment of the linker DNA, the linker DNA is linked to the termini of a double-stranded cDNA. Therefore, the termini are blunt ended by using T4 DNA polymerase. In that course, 10 to 50 nucleotides are removed, so that full-length cDNA cannot be generated, consequently. In other words, no 5′-terminal sequence is recovered. Alternatively, the method according to the present invention is specific in that an oligoribonucleotide is specifically ligated only to full-length mRNA and that immediately after reverse transcription, PCR is carried out using a primer specific to the sequence of the oligoribonucleotide, to thereby selectively amplify only cDNA comprising complete 5′-terminal sequence.

An additional aspect of the present invention relates to the sequence of an oligoribonucleotide to be replaced for the 5′-terminal cap structure removed with TAP process. The oligoribonucleotide is ligated to the 5′-terminus of mRNA and is then synthesized in the form of cDNA through reverse transcription. The oligoribonucleotide works as a attachment site of a primer specific to the oligoribonucleotide, when used. Thus, the sequence serves as a very important marker for the analysis of the complete 5′-terminus. Reverse transcription using the random hexamer, in particular, enables the collection of plural cDNA fragments derived from mRNA; hence, the sequence specificity of the oligonucleotide replaced for the cap in these fragments determines whether or not only the sequence derived from the 5′-terminus of the mRNA can specifically be analyzed. In accordance with the present invention, therefore, the designing of the oligoribonucleotide and the sequencing thereof are very significant.

For more detailed description, it is said that the nucleotide sequence on the genome of humans or mouse comprises about 3×10 9 base pairs (bp). Gene-encoding regions, gene expression regulatory regions, reiterative sequences, introns and the like are arranged on the genome and these structures function under the control of extremely sophisticated programs in the course of development. It is also considered that the sequences are never random.

For example, a structure designated “CpG island” is listed. The structure is known to be present in the 5′-region, promoter region and first exon of gene (Tanpakushitsu.Kakusan.Kouso (Protein, Nucleic acid and Enzyme), 41 (15), p. 2288, (1996)). It is known that promoters involved in gene expression or regions involved in transcription termination are enriched with AT. The following reason is very readily understandable but is just deduced; the CpG island serves as a landmark for protein as a trans-factor controlling gene expression to speedily discriminate AT rich region thermodynamically unstable from GC rich region thermodynamically stable, when the protein is going to find its attachment site from the sequences on genome.

Furthermore, it is known based on the analyses so far that the occurrence frequency of dinucleotides is biased in all living organisms. Particularly, a rule of excess CT and TG and deficiency of CG and TA is also known (Proc. Natl. Acad. Sci., Vol. 85, pp. 9630-9634 (1988)). It is thus considered that the genome sequences are never random in living organisms but include information evolved under a certain rule.

Regarding to the oligoribonucleotide for use in accordance with the present invention, therefore, the application of a sequence introduced under consideration of the bias in the sequences on genome to the analysis of the 5′-terminal sequence of mRNA can elevate the precision of the analysis of the 5′-terminus of a specific gene among an assembly of very complicated 5′-cDNA sequences.

In association with the present invention, additionally, it has been deduced that TAP quality is a very significant element. More specifically, it has been known that the cap structure can be cleaved by using TAP (FEBS Lett., Vol. 65, pp. 254-257 (1976)). The method is only one known method capable of principally verifying the cap. The TAP action absolutely certifies that RNA has the cap structure (7 mGppp) at the 5′-terminus of mRNA, namely RNA with intact 5′-terminus.

Meanwhile, it is known that RNA is handled with much difficulty, because RNase as one nuclease species consistently exposes RNA to a degradation risk. Thus, RNA experiments essentially demand the handling of RNA under suppression of the activity at the lowest limit as required. A reference (Blumberg, D. D. Method in Enz., 152: pp. 20-24 (1987), Academic Press.) for example describes in detail experimental precautions relating to the handling. Even under such precautions, it is difficult to thoroughly suppress RNA degradation. Additionally, mRNA differs from genome DNA in that mRNA is not double-stranded but single-stranded. Accordingly, RNA extracted should be handled in aqueous solvents. However, the most thermodynamically stable stem structure is formed as the RNA secondary structure in various regions within the molecule. The stem structure is a serious cause for the inhibition of reverse transcriptase reaction. The aforementioned two points serve as serious causes for incomplete conversion of mRNA sequence to cDNA.

In an additional characteristic aspect of the present invention, tobacco acid pyrophosphatase is used so as to remove the phosphate group from the cap structure at the 5′-terminus of non-full-length mRNA in the mRNA sample at the second step; the tobacco acid pyrophosphatase in particular can remove the cap structure at the 5′-terminus and is already purified at an extent with no contamination of other enzymes cleaving the remaining sites of mRNA.

Specifically, it is confirmed that TAP currently commercially available is not appropriately used for efficient sequencing of the 5′-terminus of mRNA. Because the TAP contains trace amounts of enzymes such as nuclease cleaving phosphodiester bonds composing RNA and phosphatase removing 5′-phosphate group freshly generated after cap cleavage, such TAP can never be used for selective cleavage of the cap structure in mRNA and thereby efficient sequencing of the 5′-terminus of mRNA. In accordance with the present invention, therefore, use is made of TAP being capable of removing the cap structure at the 5′-terminus and purified at an extent with no contamination of other enzymes cleaving the remaining sites of mRNA.

As has been described above in accordance with the present invention, advantageously, a rapid synthesis method of cDNA starting from the 5′-terminus of mRNA can be provided for the purpose of the analysis of the full-length 5′-terminal sequences of numerous cDNA species in a rapid manner by selectively synthesizing cDNA including the 5′-terminal sequence of full-length mRNA with the cap structure. Additionally, tobacco acid pyrophosphatase preferable for use in the synthesis method can be provided.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an explanatory diagram schematically depicting the schemes of the individual steps in the cDNA synthesis method according to one embodiment of the present inventiion;

FIG. 2 shows graphs depicting the results of the removal of the cap structure with highly purified TAP without any damage of the RNA chain;

FIG. 3 shows bar graphs depicting the occurrence frequency of CT/TG dinucleotides vs. the homolog scores of 10-mer sequences;

FIG. 4 shows bar graphs depicting the occurrence frequency of CG/TA dinucleotides vs. the homolog scores of 10-mer sequences;

FIG. 5 shows an explanatory diagram depicting the RAPD analysis results of selected primers of 10-mer sequence using human genome DNA as template vs. the homolog scores thereof; FIG. 5 a expresses group 1 ; and FIG. 5 b expresses group 2 ;

FIG. 6 depicts the sequences of 9 oligoribonucleotides functioning as primers;

FIG. 7 shows an explanatory diagram depicting the 5′-terminal analysis results of human placenta lactogen mRNA, based on human placenta 5′ cDNA;

FIG. 8 shows an explanatory diagram depicting the electrophoretic evaluation of PCR 5′-terminal cDNA derived from human placenta lactogen mRNA using the oligoribonucleotide sequence; and

FIG. 9 shows an explanatory diagram of the PCR amplification results of the transferrin receptor 5′ cDNA derived from the human placenta oligo capping cDNA; FIG. 9 a depicts the approximate sizes of speculative PCR products when two primes are used, namely TFRA3 and TFRA4; and FIG. 9 b depicts the schematic electrophoresis results.

BEST MODE FOR CARRYING OUT THE INVENTION

EXAMPLE 1

Scheme of cDNA Synthesis Method

FIG. 1 shows an explanatory diagram depicting the scheme of each step of the cDNA synthesis method according to one embodiment of the present invention. The process of the cDNA synthesis method according to the present embodiment comprises:

a first step of adding alkali phosphatase 3 to a mRNA sample containing full-length mRNA 1 with the cap structure (7 mGppp) and non-full-length mRNA 2 without any cap structure in mixture as shown in the starting step a, to remove the 5′-terminal phosphate group P of the non-full-length mRNA 2 with the alkali phosphatase, as shown in step b,

a second step of adding tobacco acid pyrophosphatase 4 to the mRNA sample to remove the 5′-terminal cap structure (7 mGppp) of the full-length mRNA in the mRNA sample by using the tobacco acid pyrophosphatase, as shown in the step c,

a third step of ligating oligoribonucleotide 5 to the 5′-terminal phosphate group of the resulting mRNA with T4 RNA ligase 6 as shown in the step d, and

a fourth step of adding to the mRNA sample, reverse transcriptase 7 and random hexamer 8 capable of being annealed to an intermediate sequence within the mRNA, to synthesize a first-strand cDNA complementary by subjecting the mRNA ligated with the oligoribonucleotide at the 5′-terminal phosphate group to a process with the reverse transcriptase using the random hexamer as primer, as shown in the step e.

More preferably, the process further conprises an additional fifth step of synthesizing a second-strand cDNA from the first-strand cDNA as shown in the step f and optionally amplifying the resulting second-strand cDNA by PCR as shown in the step g.

For example, DNA carrying the 5′-terminal sequence of the mRNA can be prepared on the basis of the cDNA thus prepared. The thus prepared DNA can ultimately attain the purpose of the present invention, when the DNA is cloned in an appropriate vector and is then sequenced. Based on the sequence of the oligoribonucleotide, furthermore, the first-strand cDNA synthesized by the reverse transcriptase reaction can be converted to a double-stranded cDNA. 5′-cDNA library can be prepared by cloning the double-stranded cDNA in for example plasmid vector or phage vector.

As has been described above, in accordance with the present invention, the 5′-terminus of mRNA can be sequenced completely for subjects of plural genes.

EXAMPLE 2

Purification and Examination of Tobacco Acid Pyrophosphatase (TAP)

In the method of the present invention, it has been revealed that the purification degree of TAP as an enzyme recognizing and cleaving the cap structure is very important for the complete sequencing of the 5′-terminus of mRNA. More specifically, TAP can be commercially available in many countries. However, the present inventor's attempts have demonstrated that the TAP commercially available can never be used for efficient determination of the 5′-terminal sequence of mRNA. The reason is as follows. So as to selectively cleave the cap structure of mRNA, it is never permitted that TAP is contaminated with even trace amounts of nuclease cleaving the phosphodiester bond composing RNA and phosphatase removing the 5′-phosphate group freshly generated after the cleavage of the cap. Such TAP commercially available is contaminated with nuclease and phosphatase, although the TAP is at some degree of purity. Thus, the TAP can never be used for efficient determination of the 5′-terminal sequence of mRNA.

In other words, these commercially available TAP products cleave RNA during the course of the cleavage of the cap structure due to the contamination of nuclease, so it has been found for the first time by a highly sensitive assay method developed by the present inventors, that these TAP products absolutely cannot be used therefor. Only the highly sensitive assay method can determine whether or not a TAP enzyme sample is contaminated with nuclease. General nuclease assay methods can never determine whether the purity of TAP is high enough for use for the determination of the nucleotide sequence of the 5′-terminus of mRNA in the vicinity of the cap. In other words, one of the essential aspects of the present invention includes high purification of TAP to remove nuclease and phosphatase from the TAP.

Alternatively, the highly sensitive assay method for purity evaluation serves as a measure to enable the high purification of TAP and determines whether or not the purified TAP can be used in the method of the present invention. The highly sensitive assay method will be described below. According to the method, TAP can be purified to prepare the high-purity TAP enzyme required for the process of the present invention.

TAP purification is already described in a reference (Biochemistry, Vol.15 (10), pp. 2185-2190 (1976)). However, present inventors removed the contaminated nuclease and the like by various combinations of column chromatographic means or by repeating a single type of chromatography, as long as the results of the activity assay by the highly sensitive assaying were not satisfactory. It should be noted that the enzyme is extremely labile and the recovery of an enzyme sample with a high specific activity is very significant for the following experiments. But the enzyme is not limited to the example herein described. More detailed explanations are as follows.

Tobacco cell BY2 was kindly supplied by Dr. Hideaki Sinshi of the Life Engineering and Industrial Technology Research Institute, the Agency of Industrial Science and Technology of Japan. The cell was cultured according to the reference described above. More specifically, as the culture medium, use was made of the Murashige-Scoog culture medium; the cell was cultured under shaking under a dark condition for 7 days; and the cell was harvested by centrifugation. In one typical example, the cell of 180 g was recovered from a 1.5-liter culture broth.

The cell was suspended in 300 mL of 200 mM NaCl, 10 m β-mercaptoethanol (β-ME), 1 mM ethylenediaminetetraacetate disodium (EDTA), and 100 mM sodium acetate, pH 5.0, and was then disrupted with Sonifier-450 (Trademark; manufactured by Bronson, Co.) while care was taken not to raise the temperature. By centrifugation, the cell debris was discarded from the disrupted cell; and the resulting supernatant was thoroughly dialyzed against 10 mM β-ME, 20% glycerin, 0.01% Triton X-100, and 10 mM Tris-HCl, pH 6.9 (25° C.).

The dialysate was subjected to chromatography on DE52 column (™; manufactured by Wattman, Co.); and the pass-through fraction was adsorbed on S-Sepharose (™; manufactured by Pharmacia, Co.). The column was sufficiently washed until no ultraviolet-absorbing materials were eluted; and the absorbed substance was eluted on a linear gradient of 0-0.5 M NaCl concentrations. As a TAP fraction, the eluted fraction was added to 1 mM EDTA containing 5 mM nitrophenyl-pT (manufactured by Sigma, Co.), 0.1% β-ME, 0.01% Triton X-100, and 50 mM sodium acetate, pH 6.0. The resulting mixture was kept at 37° C. for 10 minutes. Then, the absorbance at O.D. 400 nm was measured for the assay. Active fractions were combined together; after desalting, the resulting mixture was subjected to gel-filtration chromatography on a column of Sephacryl S-200 (™; manufactured by Pharmacia, Co.), to assay the TAP activity in the same manner as described above.

The active fractions were combined together; after desalting, the resulting mixture was subjected to gel-filtration chromatography on a column High-trap Blue (™; manufactured by Pharmacia, Co.), to elute the absorbed substance on a linear gradient of 0-0.5M concentrations. The active fractions were assayed and sufficiently dialyzed against a stock buffer (50% glycerin, 100 mM NaCl, 0.1 mM EDTA, 1 mM dithiothreitol (DTT), 0.1 mM benzamidine, 0.01% Triton X-100, 10 mM Tris-HCl, pH 6.9); and the resulting dialysate was stored at −20° C. until use. In one typical example, a TAP sample of 0.05 U/μL or mL can be recovered by the aforementioned procedures. In case that the contamination of a trace amount of nuclease was observed by the ultra-super sensitive purity assay method, the aforementioned procedures were repeated; and additionally, desalting and gel-filtration column chromatography on Sephacryl S-200 (™; manufactured by Pharmacia, Co.) were repeated.

The activity then was defined as follows; 1 U of the enzyme can release 1 μ mole p-nitrophenol during the reaction at 37° C. for one minute under the assay conditions of the activity. In the case of a commercially available TAP product (manufactured by Wako Pure Chemicals, Co. Ltd.), it is defined that 1 U of the enzyme can release 1 nmol inorganic phosphoric acid from a substrate ATP during the reaction under conditions in the presence of 50 mM sodium acetate, pH 5.5, 1 mM EDTA, and 10 mM β-ME at 37° C. for 30 minutes. As to the relative activity of the TAP sample of the present example to the commercially available product, 1U of the TAP sample of the present example for p-nitrophenol corresponds to the 367,000 U activity of the commercially available product for ATP as substrate. Thus, 0.5 U of the TAP sample recovered in the previous purification example is converted to 185,500 U. Hereinafter, the activity of TAP is expressed on conversion to the latter definition of the activity.

At that state, the level of contaminating nuclease was assayed, using as substrate 8 μg of rRNA (16S and 23S) of Escherichia coli . More specifically, the TAP corresponding to 500 U was added to and reacted with rRNA of Escherichia coli in a buffer of 1 mM EDTA, 0.1% β-ME, 0.01% Triton X-100, 5 mM sodium acetate, pH 6.0, for reaction at 37° C. for 2 hours. The RNA was electrophoresed on 0.1% agarose under a modification condition of formamide presence; the electrophoresis was terminated when a concurrently added dye xylene cyanol reached about ⅓ of the agarose gel. Under irradiation of ultraviolet ray (wavelength of 254 nm), photographs were taken, to determine the degradation degree of the RNA. The TAP sample purified by the method illustrated above contained almost no RNA-degrading activity under the condition.

EXAMPLE 3

Ultra-super Sensitive Assay Method of TAP Purity

So as to examine whether or not the purified TAP could cleave the cap structure of mRNA with no deterioration of the RNA chain, the following ultra-super sensitive assay method of TAP purity was established. Because the RNA to be treated with TAP in accordance with the present invention is mRNA with a cap structure at the 5′-terminus and with a polyA structure at the 3′-terminus, mRNA with the same structures at both the termini was prepared as a labeled form with two types of radioactive elements. Specifically, mRNA with the 5′-terminal cap structure labeled with tritium ( 3 H)-methyl (CH 3 ) group and with the RNA chain labeled with phosphoric acid containing radioactive phosphorus ( 32 P), was prepared, which was similar to intact mRNA from natural origin. The intact mRNA for use in the process according to the present invention can be expressed as follows.

(5′) m 7 Gp(↓)p(↓)pN m pNpNp . . . poly A (3′)

wherein, m represents methyl group; p represents phosphate group; N represents four types of nucleotides; and G represents guanosine; and the downward arrow represents the site for TAP cleavage reaction.

Because the mRNA is labeled at the methyl group and phosphate group with trace amounts of radioactive elements with high specific activities, namely 3 H and 32 P, the desired cleavage of the cap structure, namely dissociation of m 7 G (7-methyl guanosine) from the mRNA itself, and 32 P-nucleotide derived from the “undesirable RNA degradation due to nuclease contamination”, and dissociation of phosphoric acid containing 32 P from mRNA itself due to “undesirable phosphatase contamination” can be sharply assayed.

“ 3 H-m 7 G” and “ 32 P-nucleotide+phosphoric acid containing 32 P” were assayed by allowing TAP to react with the double-labeled mRNA, adding cold 5% trichloroacetic acid to the resulting reaction mixture and centrifuging the mixture (10,000×G, 10 min) to separate the supernatant fraction ( 3 H-m 7 G) from the precipitate fraction (mainly 32 P-RNA and 3 H-methyl derived from N m ) and separately count 3 H and 32 P with a liquid scintillation counter (manufactured by Beckman, Co.).

The assay method using mRNA labeled with “ 3 H-methyl- 32 -phosphoric acid” is ultra-super sensitive for the monitoring of contaminated nuclease; and simultaneously, the method can determine whether or not TAP practically cleaves the cap structure. The method provides an important marker as to the practical purity of TAP during purification for the invention.

The ideal assay results by the method are such that “50% of the tritium radioactivity of 3 H-m 7 G as the cleavage product of the cap structure transfers to the supernatant; and 100% of the 32 P radioactivity in RNA remains in the precipitate fraction”. Such ideal results could never be yielded when the TAP purified by us at the early stage or commercially available TAP products were used. As the consequence of the repetition of the aforementioned purification procedures, finally, we obtained a high-purity TAP sample at a level usable in accordance with the invention. The method for preparing radioactively double-labeled mRNA with “ 3 H-methyl- 32 P-phosphoric acid” and the method for assaying the mRNA will be described below.

(3.1) Preparation of poly-A mRNA Radioactively Double-labeled with 3 H-methyl- 32 P-pU

Vaccinia virus contains, in its virus particle, various enzymes synthesizing virus mRNA with a cap structure and poly-A. The virus synthesizes about 50 types of mRNAs. These mRNAs can be used as model mRNA, because the mRNAs are very similar structurally to mRNA in higher animals and plants including humans (S. J. Higgins and B. D. Hames, RNA Processing, A Practical Approach, Vol. 11, pp.35-65, (1994)). The virus particle was purified by a method comprising infecting vaccinia virus with HeLA cell and recovering the virus particle from the infected cell by using glycerin-density gradient ultra-centrifugation (Wei, C. M. and Moss, B., Proc. NatI. Acad, Sci., Vol. 72, PP. 318-322, (1975)).

32 P-labeled mRNA was recovered from the reaction of the purified virus particle (about 100 μg) in a 0.5 mL reaction solution containing 100 mM Tris-HCl, pH 8.0,12 mM MgCl 2 , 4 mM ATP, 2 mM GTP, 2 mM CTP, 0.1 mM UTP, 100 μCi (α- 32 P) UTP (specific activity; 3,000 Ci/mM), 1 mM S-adenosylmethionine, 30 mM β-mercaptoethanol, 280 U/mL RNasin and 0.5% NP-40 at 37° C. for 2 hours.

Similarly, 3 H-methyl-labeled mRNA was recovered from the reaction of a replicate of the virus (about 100 μg) in a 0.5 mL reaction solution containing 120 mM Tris-HCl, pH 8.0,12 mM MgCl 2 , 4 mM ATP, 2 mM GTP, 2 mM CTP, 2 mM UTP, 50 μCi 3 H-S-adenosylmethionine (specific activity of 78 Ci/mM), 30 mM b-mercaptoethanol, 280 U/mL RNasin, and 0.5% NP-40 at 37° C. for 2 hours.

After these reactions, the individual reaction solutions were extracted in phenol; and the synthesized RNAs were subjected to Sephadex G-100 column chromatography and thereby separated from unreactive substrates. By affinity chromatography with oligotex (dT) 30, RNAs with poly-A were purified and isolated. The aforementioned two types of RNAs were used for the purity assay of TAP of a single type or in mixture.

(3.2) Highly Sensitive Assay Method of TAP Purity

In the course of purification, TAP was examined by the following method. Specifically, 1 μL of the purified TAP (300 units) was added to and incubated in a 20 μL reaction solution containing 1×TAP buffer, 32 P-RNA (4,000 cpm; about 1 ng) or 32 H-methyl-RNA (2,000 cpm, about 1 ng) at 37° C.; and then, the degradation of 32 P-RNA or the cap cleavage (decapping) reaction in the 3 H-methyl-RNA was assayed within a given period of time. After the reaction, 5 μg of tRNA was added to the reaction mixture, followed by addition of cold 5% trichloroacetic acid solution and centrifugation, to assay the radioactivities in the supernatant fraction and the precipitate fraction.

Additionally, a method for detecting a trace amount of a RNA strand with one nick inserted therein (RNA nick detection method) was carried out, by allowing 32 P-mRNA to react with TAP and thereafter assaying the change of 32 P-mRNA after the termination of the reaction, by utilizing the affinity of the 3′-terminal poly-A with the (dT) 30 region on the oligotex (dT) 30. The three types of assay methods described above are separately used in a dependent manner to the purification degree of the TAP enzyme; at the highest purification stage, a combination of the 3 H-methyl RNA/TCA method and 32 P-mRNA/nick detection method was used for the final determination as to whether or not the resulting TAP enzyme could be used for the second step of the process according to the present invention. The combination is the most highly ranked for such determination.

The data of examples using the two methods are shown in FIG. 2 . FIG. 2 shows graphs depicting the results of the removal of the cap structure with the highly purified TAP without damage of the RNA chain; the ordinate represents the detected radioactivity in % and the abscissa represents time (minute). The enzyme used was highly purified TAP; and the substrate was the mRNA of vaccinia virus. Open circle represents the cap cleavage reaction of 3 H-methyl-RNA and closed circle represents the nick activity assayed by using 32 P-mRNA. At the early stage of the research works for the present invention, furthermore, it was concluded that the purified TAP enzyme could be used practically for the present invention. Thereafter, the simple method using rRNA of Escherichia coli was used generally for purity assay.

EXAMPLE 4

Designing of Oligoribonucleotide Sequence

Furthermore, an oligoribonucleotide sequence to be ligated to the complete 5′-terminus of mRNA cleaved with TAP was designed. Thus, the invention has been achieved.

An oligoribonucleotide sequence found in cDNA as rarely as possible and with a high specificity is essentially selected and attached. Therefore, then, a 10-mer sequence for use for the RAPD (random amplified polymorphic DNA; Nuc. Acids Res., Vol.18, pp.6531-6535 (1990)) was designed. The occurrence frequency of the designed sequence was then calculated and expressed in numerical figure, to weigh the sequence.

As such 10-mer sequence, the 48,502-bp nucleotide sequence of Escherichia coli λ phage was grouped per 10 bases. Because of the presence of the circular structure, sequences carrying a 6-base sequence recognizable by restriction enzymes were excluded from the resulting sequences; and then, sequences at a GC content of 50% and with 3′-terminal G or C were extracted. In such manner, 450 sequences of 10 bases were extracted, which carried sequences satisfying the conditions for use for RAPD.

By using the high-speed homology search function in the data base software GENETYX-MAC/CD Ver. 22.0.2, a homology search of the resulting 450 sequences of 10 bases was carried out with the data base of eucaryotic organism-derived sequences of 69,936,993 bp in total among the nucleotide sequences included in EMBL-GDB release 34.0 (1993); the total number of sequences completely matching with or differing by one base from one of the 10-mer sequences was defined as homolog score. Additionally, the biological organism as the search subject was an organism with the cap structure and polyA sequence.

A homolog score of for example 1,000 means that the total number of sequences completely matching with or differing by one base is 1,000 among the sequences of 69,936,993 bp in total. The program for use in the homolog score calculation is based on the Lipman-Pearson method (Lipman, D. J. and Pearson, W. R., Science, 227: pp.1435-1441, 1985).

In Tables 1 to 5 below, 450 homolog scores are aligned in the decreasing order of the score, where the score, primer and nucleotide sequence of each are shown. FIG. 3 shows an explanatory diagram depicting the occurrence frequency of CT/TG dinucleotides vs. the homolog score of 10-mer sequence. FIG. 4 shows an explanatory diagram depicting the occurrence frequency of CG/TA dinucleotides vs. the homolog score of 10-mer sequence. In FIGS. 3 and 4 , the abscissa represents 450 sequences of 4,500 bases in the decreasing score order; and the ordinate represents dinucleotide occurrence frequencies plotted in %, namely the CT/TG occurrence frequency ( FIG. 3 ) and the CG/TA occurrence frequency (FIG. 4 ), in 20-bp units by one-base shift along the left to right direction.

The frequencies of the dinucleotides in sequences with large homolog scores and sequences with small homolog scores were examined. Thus, it was confirmed that the rule of CT/TG excess and CG/TA deficiency was satisfactorily applicable (FIGS. 3 and 4 ). More specifically, a correlation was observed such that numerous CT/TG dinucleotides emerged in sequences with large homolog scores and the occurrence frequency of CG/TA dinucleotides was high in sequences with small homolog scores.

The following sequences are set forth in Tables 1 to 5:

SEQ ID NOS. 19 TO 108 for the sequences set forth in Table 1;

SEQ ID NOS. 109 to 198 for the sequences set forth in Table 2;

SEQ ID. NOS. 199 to 288 for the sequences set forth in Table 3;

SEQ ID NOS. 289 to 378 for the sequences set forth in Table 4; and

SEQ ID NOS. 379 to 468 for the sequences set forth in Table 5.

TABLE 1
	Prim-	Nucleotide			Nucleotide
Scores	ers	sequences	Scores	Primers	sequences
7,786	A-34	CTGGAGAAAC	4,128	D-41	CCTGTTTCTC
6,165	F-29	TCTGAAGAGG	4,126	B-07	TCAGCAACTG
5,852	E-22	TTTCTCCTGC	4,121	B-36	CCGAAAGAAG
5,849	D-48	TGCTGGAAAG	4,093	A-05	GAGGTGAATG
5,611	C-24	TGCGGGAAAC	4,052	H-25	GTCATCAAGC
5,603	F-47	AGGGAAAAGG	4,047	D-03	TGTTTTCCCC
5,599	A-19	ACTGCTGAAG	4,041	H-10	ATTTCTGCCC
5,516	A-32	AACAGAGGAG	4,039	H-19	CAGCTCTTTC
5,341	X-34	ATCCTCTTCC	4,020	E-13	AAACCACAGC
5,316	F-03	ACATCAGCAG	4,019	H-40	CACTCTTCTC
5,310	A-33	GAGAAGAGTG	3,995	B-48	CTTTCTGTCC
5,185	F-05	GAGAAACAGG	3,972	X-40	CGAAAACCAG
5,145	B-10	ACTGAGGATG	3,958	G-01	CTGCTTTTCC
5,080	G-25	ACAAAGGAGG	3,951	B-23	GAATGAAGCC
5,059	B-40	AGGAAGACAG	3,943	C-13	TTGCTGAGTG
5,028	F-33	GACAAGGATG	3,915	B-22	GTTTCTGGTG
4,939	A-16	TGAGGAAAGC	3,903	C-37	GACCAAAGAC
4,914	D-49	TTCTGCTTCC	3,890	E-42	ATTCCTGTGG
4,681	C-33	GGAAAAGCAG	3,888	D-35	GAGACACAAC
4,638	G-28	GGACAGAAAG	3,879	F-01	CCCAAAACAC
4,567	D-50	AGACCATCTC	3,856	D-42	GTGTTTGTGC
4,537	E-26	GTGACAGAAG	3,840	E-31	TTTGCTCCAG
4,532	H-39	GTTTCTCCAG	3,839	A-21	CTGATGACAG
4,522	E-07	ACAACAAGGC	3,831	H-31	TTCAGAGGTG
4,497	B-20	GTGGTGAAAG	3,831	C-01	AAAGGTGAGC
4,496	E-04	TTCCTTTCCC	3,826	D-45	ATCACACACC
4,470	H-21	TTTCCTCACC	3,807	H-34	GAATGCCAAC
4,447	E-46	ACCACCAAAG	3,800	C-49	CAGTGATGAC
4,445	E-27	AATCCAGCAG	3,793	C-04	GTGACTTCTG
4,428	B-09	GAAAGAGCTG	3,792	C-14	TGCTGAACAG
4,414	B-49	TTCTGTGGAC	3,789	F-10	GTTTCAGGAG
4,394	E-49	AAAAGGCAGG	3,788	G-50	TGTCATCAGC
4,388	H-06	CACCAGAAAC	3,786	E-40	ACACAGGAAC
4,351	C-22	TGAGGTGAAC	3,775	H-47	TCATCTGCTC
4,345	D-29	CTCCTGAAAC	3,775	B-35	AAAGCAGACG
4,317	C-11	TTCTCAGGAG	3,756	F-17	AAGTCAGAGG
4,301	B-27	CCTGAAACTG	3,745	H-23	CAAATGCCAC
4,279	D-07	ATCTGGGAAC	3,712	A-26	TGAGAGTGAG
4,274	A-22	CAGAAAGACG	3,709	B-47	AATGCCAACC
4,256	E-45	ACTCCTTCAG	3,689	B-17	TGTGGAGTTC
4,256	C-34	TGAAACCAGC	3,685	C-28	CAGAAGTCAC
4,246	C-45	TGTCTTTGCC	3,659	H-38	TTTTCTGCCG
4,229	E-48	CAATGCTGAG	3,656	G-46	AATCTGCTCC
4,223	E-02	TGAGAGATGG	3,642	G-35	ATCCAGTTCC
4,211	A-06	TGGTGAAGTC	3,641	F-04	GCACAAACAC

TABLE 2
	Prim-	Nucleotide			Nucleotide
Scores	ers	sequences	Scores	Primers	sequences
3,638	E-09	TCACACCAAC	3,232	H-05	GGCTTCATTC
3,636	X-29	CGTCTTTCTG	3,227	D-02	TCAAACAGGG
3,631	X-32	CTGTCATCAG	3,215	A-14	AAACACCACG
3,611	H-08	CTTTCACCAC	3,212	F-07	GTTGTGTCTC
3,807	B-33	TGATGACCAG	3,209	G-08	AATCAGCCAC
3,603	E-25	GCAAATGGTG	3,208	E-01	CTCAGCATTG
3,583	D-47	GTGTTTTGGG	3,208	B-11	ACTGAACTCC
3,570	E-18	CTTCTGTCAC	3,186	X-35	ACTGAGATCC
3,567	D-33	ATGGCTGAAC	3,174	H-36	TCTTTGCTCG
3,563	E-47	ACAAGGTCAC	3,169	C-16	AGGGCAAAAC
3,561	F-24	GAGCAGATTG	3,164	A-49	TGAACTGGTC
3,552	F-40	GTCATCACTG	3,161	X-03	CTTTCTACCC
3,542	B-14	GATTCAGAGC	3,154	G-15	TAAGCCATCC
3,530	H-42	TCAGACCATC	3,144	A-12	CTGGTTTTCG
3,525	F-12	GATTCAGAGG	3,095	G-06	TTGCCACTTC
3,518	A-03	AATGCCAGAG	3,084	C-07	TTGTTCCCAG
3,518	A-02	GGAACTGAAG	3,077	C-27	GTGAATGGTG
3,508	C-06	GAAACTGAGC	3,070	X-02	TGGATTGGTC
3,501	C-32	TCTGGTTCTC	3,070	C-44	ACAGAGGTTC
3,491	B-05	AAAAAGGGGC	3,059	G-38	CCACAAATCC
3,480	H-20	ACCAGTTTCC	3,058	D-43	AGTCCTGAAC
3,477	E-16	CATCAACCAG	3,047	B-44	GGTGAGTTTG
3,456	G-19	GCTCAGTTTC	3,046	F-35	ACTGACACAG
3,448	D-21	TGGATGAACG	3,038	A-44	GTGAGTTCAC
3,438	C-09	TTTCTCTCGG	3,035	E-23	TCTGGTTTCG
3,433	H-16	GCTCTGAATC	3,033	D-04	TTTGTGCCAC
3,424	H-32	ACTTTCTCCG	3,024	H-28	GTGAACTCAC
3,414	H-24	TTCACCAGTG	3,018	F-11	AACACATCCG
3,388	G-30	CTGCTCAAAC	3,015	X-14	GTACAAGTCC
3,386	A-42	ATTGCTCAGG	2,976	G-13	AGGTGGTTTC
3,360	G-33	AGTTCTGCTC	2,969	E-41	AGCCATTCTG
3,342	H-01	CGGAAAAGTC	2,966	B-41	GGATTTGTGG
3,329	X-04	TTTTGGCTCC	2,965	A-35	TGAACACACC
3,317	H-02	CAGTTTCAGG	2,964	D-11	AAGAGTGGTG
3,314	F-49	GTCTTTGGTC	2,960	X-46	CATTCACCTC
3,304	C-36	GAAAGAGTGG	2,957	A-17	TGGCTGATTG
3,296	A-46	GGTGAACAAC	2,944	F-50	CCACTCTTTC
3,289	X-18	GATCTCAGAC	2,938	G-48	TGAACTGTGC
3,284	B-18	CTACAATGCC	2,932	A-47	GCTTGATGAC
3,284	A-27	CGTGTTTGAG	2,910	A-50	GTGGCATTTG
3,276	D-28	CCTCTGAATC	2,908	G-20	TGCTCAGTTG
3,269	G-31	CAAACTCACC	2,906	X-41	GGATTCACTG
3,268	B-03	TCCCTGTTTG	2,894	F-38	TGAAATGCCC
3,256	H-44	AACATCTGGC	2,883	D-32	AAACAGGTGC
3,250	X-50	CTTCAGTTCC	2,878	G-07	CGCTGAAATC

TABLE 3
	Prim-	Nucleotide			Nucleotide
Scores	ers	sequences	Scores	Primers	sequences
2,874	F-13	CTGATTCAGG	2,494	G-42	ATTTCAGCCG
2,863	D-40	TGGTTTTGCG	2,485	H43	CTATCCAGTC
2,857	B-45	GTTTGAGCAG	2,480	F-36	TGAGGTTTGC
2,854	F-22	AAAGTGCCAC	2,478	A-45	GATGAGTTCG
2,846	D-44	ACATTGGCAG	2,474	A-15	CTTACCTGAC
2,828	G-43	CTTCTTTCGG	2,451	H-26	GTTGTTCACC
2,827	E-19	CACCATTTGC	2,444	E-34	ATACACCCAC
2,825	X-24	GATCATGGTC	2,442	B-42	GTATCAGGAG
2,808	G-37	CTCCTGATAC	2,433	B-21	CAGTGGTATG
2,798	B-28	CACTTTTCCG	2,425	D-27	CCTGAATCAG
2,795	D-08	CATCCTTGTC	2,410	C-46	TGACAGTCAC
2,791	G-05	CACCATTCAC	2,409	A-29	GACTGGATAG
2,770	H-22	GTAATGGTGG	2,405	E-36	TTTGTCACCG
2,770	C-39	AGCCAGTTTC	2,384	E-14	AATGGTCTGC
2,762	C-19	ACAGTGCTAC	2,364	H-49	AAAAGACCCG
2,761	D-15	CAATCTGCTC	2,325	X-08	TGGTAAAGGG
2,742	A-25	AATGACAGCG	2,323	A-37	CATTACCAGC
2,726	X-30	TACTGTTGCC	2,321	X-17	GATCTGACAC
2,721	C-31	GGAACTACAG	2,321	F-48	TTCATTCCCG
2,718	B-50	TGAACAGGTG	2,314	G-09	CATTACTGCG
2,712	X-42	ACTTTTGGCG	2,312	A-40	CTACAAGTCC
2,699	H-48	ATTTCTGCGG	2,308	H-07	CATACCACTG
2,684	E-08	TCAACATCGC	2,292	G-12	TCACCCTTTG
2,661	E-29	AGCACAATGG	2,283	C-04	TTTGAGCACG
2,656	X-05	GGAACCAATC	2,276	F-16	AAACCTGTCG
2,649	E-24	TGCCTCATTG	2,273	X-15	GTACCAGTAC
2,649	B-04	TCTTGAGCAG	2,253	G-17	GACAATCTGG
2,648	E-35	AAAGGCATCG	2,253	E-44	GCTGTATCAG
2,644	C-38	AGGCAAACTG	2,241	C-29	CGTGAGTTTC
2,628	H-46	CTCAAACACG	2,235	C-10	TGCCAGTATG
2,628	H-13	ACCTTTCACC	2,232	H-14	GGCATTGTAG
2,615	C-03	GAAACTCACG	2,231	X-38	GTCAGGTAAG
2,612	C-25	GATTTCAGCG	2,223	D-13	GCAAGTGTAG
2,612	A-39	GTTGGCATTC	2,213	B-34	GTCCTGATAC
2,606	E-50	TTTTCTGCGG	2,210	H-03	CATACCAGAC
2,585	X-23	CATCTGACTG	2,173	D-14	TTTCACACCG
2,571	C-23	TTGGCTGTAC	2,170	X-12	CTGCTTGATG
2,571	A-09	CCGTGAAAAG	2,168	X-39	GACAATCTGC
2,570	A-13	GCAGATTGTC	2,168	H-27	CGAACTCATC
2,559	D-38	TTGCAGGTTG	2,165	X-01	TACAACGAGG
2,551	C-08	CCAGATTGTC	2,152	G-44	GTATCAGGAC
2,548	E-30	CTGGTTGATG	2,143	F-09	GCGTTTGATG
2,530	B-02	CCACCATTAC	2,134	H-35	GCTGGTAATG
2,510	E-20	AGTGACATCG	2,130	C-02	CAGTATCAGC
2,506	G-22	AATCTCACCC	2,127	H-18	GAAAATCCGC

TABLE 4
	Prim-	Nucleotide			Nucleotide
Scores	ers	sequences	Scores	Primers	sequences
2,109	A-10	CAGTGAATCC	1,692	E-06	GTAAACTCCG
2,104	G-21	TGAAAGTCCG	1,689	A-20	GTGCCTTATC
2,095	A-11	AAATGGACGC	1,684	F-28	ACCCTATCTC
2,089	X-37	AGCAGATACG	1,622	G-40	TGTAATCCGC
2,084	D-24	TTATCCCCTG	1,615	F-10	CACTAACACC
2,066	B-15	CAGTATGGTG	1,614	F-45	CCACTATCTG
2,033	B-31	TCAGATTGCG	1,611	A-23	GGAGTTTACG
2,031	F-44	GCTTACTTCC	1,609	F-27	GTGCTTTACG
2,017	D-25	CACTAAAGGG	1,608	H-15	CACCATACTG
2,005	D-46	GCTCAGTATC	1,595	A-30	GAAACGATGG
1,990	C-50	TATGTGAGCG	1,594	E-33	ATTTGGTCGG
1,987	D-26	TCGCATCAAC	1,588	C-41	CAGATAGTGG
1,976	F-02	GATACTGAGC	1,574	B-24	AGTGCTTACC
1,965	F-26	CTACACTTGC	1,566	F-20	CACGGAAATG
1,961	B-26	GTCTGGTATG	1,531	F-23	TTCGGTGATG
1,946	B-12	GCGGATTTTC	1,521	X-33	GATAAGGCAC
1,935	F-39	GTTTACCTCC	1,517	G-02	CTGTAGTTCC
1,924	C-15	AGGGGAATAC	1,516	H-04	CCACGTTTTC
1,914	E-05	CTGATACAGC	1,500	C-12	TGATTGGTCG
1,913	D-30	CATCAAACGC	1,493	E-39	GGTGTTAGTG
1,913	C-35	ATTCGTGGAG	1,490	H-29	CATCGTGTTG
1,899	X-43	CTTTTCACGG	1,486	X-28	CGTAAACTCC
1,897	D-12	CGTAAAGCAC	1,486	F-14	CCCTTTAGTG
1,893	D-01	GGAGGTAAAC	1,480	C-21	CGCAGTAATG
1,889	E-43	CGGAGTTTAC	1,476	F-18	GCAGATTACG
1,835	H-30	ACTTGTCACG	1,472	X-36	CCCGTTTTTG
1,827	C-05	AACGAGAGAG	1,455	B-30	CAAAACGCTG
1,825	X-49	TGACTGTTCG	1,447	D-37	GCTCAATACG
1,825	D-16	CCCCTATTTG	1,440	G-16	TTCGCTGATG
1,821	B-16	ATGACTACCG	1,424	X-48	TTAGCATCCG
1,820	G-39	ACTGTTTCGG	1,419	H-17	TATCGCTGTC
1,816	F-37	TGACGGCAAC	1,418	H-50	ACGGGTAAAG
1,814	G-14	AGGTAAAGCG	1,418	D-23	TACACCGAAC
1,811	B-46	GGCTATTCTC	1,406	G-29	GAGAATAGCC
1,792	B-25	GAAAACGTGG	1,403	A-08	ACTAATGGGC
1,772	A-28	TTTATGGGGC	1,390	G-23	AATAGCCTCC
1,760	F-19	TAGTTGCCTG	1,374	F-08	CCTAATCAGC
1,746	F-32	TCGGATTTGC	1,372	X-27	GTGATAACCG
1,743	D-18	AGTGGGTTAC	1,371	X-26	GATCTAAGGC
1,737	G-26	GCTGATACTG	1,357	B-19	GAGTCCTATG
1,735	H-09	TTTCACCGTG	1,354	X-06	AAACTCCGTC
1,725	H-33	GGACTTGTAG	1,354	F-06	CGTATTGAGC
1,711	D-05	TCTGACGATG	1,352	H-12	AGTCAACGTC
1,701	A-18	CAAAAACGGG	1,340	D-34	GCTGATTAGG
1,699	A-36	AGTGTAAGGG	1,339	F-21	CAAATAGGGG

TABLE 5
	Prim-	Nucleotide			Nucleotide
Scores	ers	sequences	Scores	Primers	sequences
1,338	B-01	AGCCGAAATG	1,023	X-44	TGTTATCCCG
1,337	C-48	CGTTATGAGC	1,001	X-13	GTTTTCGCAG
1,327	X-19	GATCATAGCC	987	E-32	ATTCGCAGTG
1,319	F-46	TTTTTCCGCC	979	E-37	GAACGGATAC
1,319	D-22	CGTAATCTGC	979	A-48	ACCGTGATTC
1,312	A-04	ACTGATACCG	973	D-10	GCGGTAAATC
1,305	A-41	TTTCTGCGTC	956	A-01	CTGTCGTTTC
1,304	D-17	CATTTCCGTG	955	A-07	CCGACTATTC
1,304	C-20	CAGCGATTTC	952	X-21	GATCTAACCG
1,302	A-24	CGGTTATCAC	951	B-13	AATACACGGG
1,292	G-10	GAAATCGCTG	948	D-09	CATCCGTTTG
1,291	B-08	TATTGAGCGG	930	D-06	CACGAATGTC
1,281	C-43	ATGAACGGTG	917	E-03	ACCGTTGTTC
1,251	B-39	ATGAAGCGAC	883	A-31	TGCGACAATC
1,249	X-10	GGTACTAAGG	872	X-09	TCGGTCATAG
1,249	A-38	AGTGCGAAAG	839	B-06	AGCGTTCATC
1,246	H-11	CATAGGACTC	822	B-37	AGAGCGATAC
1,238	G-11	GTATGACGAC	821	E-28	GTAACGCAAC
1,236	G-47	CAGCGTTTTG	805	G-24	ATAACCGCAC
1,228	X-07	TCGATACAGG	799	X-31	ACCCGTTTAC
1,228	F-30	GATTTACCGC	791	X-16	GATCACGTAC
1,205	C-42	GGAAGTAAGC	784	H-37	ACGGTCATAC
1,193	G-27	TTCGTTCTGC	765	D-19	TATTGACGCC
1,180	A-43	CAACACGATG	765	C-18	GTCGTCATAC
1,179	F-31	CAAACGGATG	762	E-38	CAATAGCGAC
1,179	E-15	TTACGCTGTG	754	G-18	AATACGCCAC
1,175	H-45	TGCTCATACG	745	C-47	GTTTACGGTG
1,162	B-32	GCGTATGTTG	744	D-39	TCTACTCGTG
1,158	X-20	GATCAATCGC	730	C-30	TGACCGTAAC
1,143	D-31	ACGGGTAATG	718	B-43	GATTTACGCG
1,128	B-29	AAAGTCCGTG	713	E-12	GTATCCGTTC
1,124	D-36	TGTTATGCCG	709	F-15	ACATACGAGC
1,117	X-47	ACGGATGTAG	696	F-42	CACCGTAAAC
1,109	C-17	AAACGCTCTG	694	G-41	GTTCGTAAGC
1,097	H-41	CCATCGTTTC	693	C-03	TCCGTATGTC
1,090	G-49	AAATGACGCC	680	G-34	TGCGACATAC
1,083	G-36	ATCGCCATAC	677	G-32	CCCGTAAATC
1,082	F-43	TAAAACGCCC	673	E-11	GTCGCTATTG
1,078	F-34	GACATTCGTG	640	E-21	TGATTAGCGG
1,076	F-41	GCTCATAACG	634	C-40	TGACGATAGC
1,070	G-45	CAACATACGC	616	B-38	GCTTACGAAC
1,066	X-25	GATCATAGCG	609	X-45	GAATAGTCGG
1,062	X-22	GATCGCATTG	581	E-17	GTTGCGTTAC
1,059	D-20	ACCAAACGAC	551	C-26	ACAGCGTATG
1,048	X-11	TACCTAAGCG	526	F-25	ATGCGTAAGG

For the purpose of confirming the analysis results, the resulting 450 sequences were used for the RAPD analysis using human genome- or mouse genome DNA; depending on the amplification degree of PCR products and the number of ladder (complexity), sorting was performed; among them, several sequences with lower amplification degrees and less ladder patterns (group 1 and several sequences with higher amplification degrees (group 2 ) were selected for PCR. FIG. 5 shows an explanatory diagram depicting the RAPD analysis results of the selected primers of 10-mer sequence and human genome DNA as template vs. the homolog scores. More specifically, all the 450 sequences of 10-mer were subjected to RAPD analysis and classification, depending on the basis of the difference in pattern. From 10mer sequences with less RAPD patterns (group 1; FIG. 5 a ) and 10-mer sequences with more RAPD patterns (group 2; FIG. 5 b ) were sampled several sequences, for additional RAPD.

Consequently, as almost expected but with some exception, a correlation in the amplified PCR product pattern was observed between the group of the primers with large homolog scores and the group of the primers with small homolog scores, when used ( FIGS. 5 a and 5 b ). The total score of each of the groups is shown, and apparent difference is observed.

The results indicate that such analysis is meaningful even if the sequences registered in the data base used were biased severely and that such analysis provides efficacious information for the analysis of enormous genes, such as genome analysis.

Based on the aforementioned results, an oligoribonucleotide was designed from the following two standpoints.

Firstly, a sequence of a small homolog score is referenced because a sequence of a smaller homolog score is estimated to be at a low occurrence frequency of the sequence on genome.

Secondly, the ligation efficiency of a DNA fragment treated with a restriction enzyme forming a blunt end is known to below. Thus, it was deduced that the ligation efficiency of the end of an oligoribonucleotide to the 5′-terminus of TAP-treated mRNA would vary, depending on the end.

From the two standpoints, 7 oligoribonucleotides were prepared. FIG. 6 shows the prepared 7 oligoribonucleotides, compared with the sequence of vectorette (Nuc. Acids. Res., Vol.18, pp.2887-2890 (1990)). In the figure, the title of 10-mer sequence is shown in parenthesis underneath each of the sequences. Additionally, the sequences of the oligoribonucleotides of 8 in total, as shown in FIG. 6 , are listed as SQ ID Nos. 1 to 8 in the sequence listing table. Herein, the individual oligoribonucleotides were synthesized and purified by HPLC (Nippon Gene Co., Ltd. Custom Synthesis Service).

The first 7 oligonucleotides are composed of the entirety or a part of a series of sequences with small homolog scores shown in Table 5. For example, the oligoribonucleotide “GG” is composed of a series of three 10-base sequences (E-17, C-26, F-25; T is modified into U) with the smallest homolog score.

EXAMPLE 5

Synthesis of Human Placenta 5′ cDNA and Analysis of 5′-terminus of Human Placenta Lactogen mRNA

The sequence of the 5′-terminus of mRNA of for example human placenta lactogen was analyzed. Human placenta immediately after delivery was frozen as soon as possible and was then used as a starting material for RNA extraction. The frozen placenta was immersed in liquid nitrogen and finely disrupted so as to avoid the thawing thereof under caution; the resulting placenta was placed, as it was frozen, in a guanidine thiocyanate solution and solubilized with Polytron homogenizer, from which the total RNA was extracted. From the total RNA was extracted polyA+ RNA on oligodT cellulose (Gibco BRL Co.).

In a typical example, the total RNA can be recovered at a yield of 2.5 mg from 10 g of human placenta issue; poly-A + RNA can be extracted at a yield of 0.06 mg from the total RNA of 6 mg. For more additional description, the separation method of RNA is not limited to the method herein listed; for example, the method is described in detail in Method. In Enz. Vol. 152 (1987 ), Academic Press.

As described below, human placenta 5′-cDNA was synthesized.

Step 1: Dephosphorylation of 5′-terminus of Non-full-length mRNA

A reaction volume of 100 μL containing 5 pg of human placenta poly-A + RNA, 0.1 M Tris-HCl, 10 mM DDT, pH 7.6,160 U RNasin (Promega Co.), and 10 U alkali phosphatase (CIAP, Nippon Gene Co., Ltd.) was prepared and kept warm at 37° C. for 30 minutes. For the purpose of protein denaturation in the solution to inactivate alkali phosphatase and purify RNA, phenol treatment once, chloroform treatment once and ethanol precipitation once were carried out. After the reaction, the resulting solution was dissolved in 50 ∞L of H 2 O treated with diethylpyrocarbonate (referred to as DEPC-H 2 O hereinafter) after reaction.

Step 2: TAP Treatment

To 50 μL of the solution containing RNA after CIAP treatment were added 10×TAP buffer (500 mM sodium acetate, pH 5.5, 50 mM EDTA, 100 mM β-ME), 160 U RNasin, and 300 U TAP; by using DEPC-H 2 O, the resulting solution was adjusted to a final reaction volume of 100 μL, for reaction at 37° C. for one hour. Through phenol treatment once, chloroform treatment once, and ethanol precipitation once, the resulting reaction mixture was dissolved in 33.5 μL of DEPC-H 2 O.

Step 3: Oligoribonucleotide Ligation with T4 RNA Ligase

10 μg of an oligoribonucleotide (AA described in Example 2 was used herein; AA: GUUGCGUUACACAGCGUAUGAUGCGUAA), 10×T4 RNA ligase buffer (500 mM Tris-HCl, 100 mM MgCl 2 , 10 mM β-ME, 10 mM ATP), 0.5 μL of 100 mM ATP, 160 U RNasin, and 250 U T4 RNA ligase (New England Biolab. Inc.) were added to and thoroughly mixed with 33.5 μL of the CIAP/TAP-treated RNA prepared at the step 2 to a final reaction volume of 50 μL; then, 50 μL of 50% polyethylene glycol 6000 (PEG 6000) was added to the reaction mixture to a final PEG concentration of 25%; and the resulting mixture was kept warm at 20° C. for 16 hours.

So as to decrease the viscosity due to PEG after the termination of the reaction, 200 μL of DEPC-H 2 O was added to the reaction mixture, followed by thorough agitation to decrease the viscosity. Subsequently, phenol treatment once and chloroform treatment once were carried out. Then, 1 μL of Ethachinmate (Nippon Gene Co., Ltd.) and 30 μL of 3M sodium acetate were added to the resulting solution, followed by blending and subsequent ethanol precipitation. The precipitate was recovered and dried, which was then dissolved in 100 μL of DEPC-H 2 O, followed by addition of 50 μL of ammonium acetate for ethanol precipitation. The ethanol precipitation procedure was repeated three times. Finally, the resulting ethanol precipitate was dried and dissolved in 50 μL of DEPC-H 2 O, which was defined as oligo capping purified RNA, in which the oligonucleotide was replaced for the cap structure.

Step 4: Synthesis of First-strand cDNA

To 50 μL of the oligo capping RNA as template was added 5 μL of 20 μM random hexamer; and the resulting total volume of 55 μL was kept warm at 70° C. for 10 minutes and then cooled on ice; to the resulting solution were immediately thereafter added 20 μL of 5×First -strand buffer (manufactured by Gibco BRL, Co.), 10 μL of 0.1 M DTT, 20 μM dNTP mixture solution, and 5 μL of RNasin to a final volume of 95 μL, which was kept warm at 37° C. for 2 minutes; immediately thereafter, 5 μL (1,000 U) of Superscript II (manufactured by Gibco BRL, Co.) was added to the resulting mixture, for 30-min reaction at 37° C. After the reaction, the mixture was kept warm at 95° C. for 10 minutes to inactive the enzyme, followed by addition of 400 μL of DEPC-H 2 O, to prepare 500 μL of human placenta oligo capping cDNA.

The human placenta oligo capping cDNA thus prepared was examined by analyzing the sequence of the 5′-terminus of the mRNA of placenta lactogen.

Human placenta lactogen, a peptide hormone belonging to the growth hormone gene family and of a molecular weight of 22 kDa, forms a cluster on the human chromosome 17. The expression mode and the like are now researched progressively (Genomics, 4(4): pp.479-497 (1989)). As to human placenta lactogen, additionally, it has already been reported that transcription products with different transcription starts are present in the placenta (Biochem. Int. 16 (2) pp.287-292 (1988)).

Step 5: Synthesis of Second-strand cDNA

Using a gene-specific primer ASP1:

(5′-GTTGGAGGGTGTCGGAATAGAGTC-3′)

prepared from the placenta lactogen gene and an AA oligo-specffic primer RC5′:

(5′-GCGTTACACAGCGTATGATGCGT-3′)

comprising a partial sequence within the AA oligo, PCR was carried out. The sequences of the primers ASP1 and RC5′ are shown as SQ ID Nos. 9 and 10, respectively, in the attached sequence listing table. More specifically, 1 μL of human placenta oligo capping cDNA, 5 μL of 10×GeneTaq buffer (Trademark; manufactured by Nippon Gene Co., Ltd.), 5 μL of 2.5 mM dNTP mixture solution, 2 μL each of ASP1 and RC5′ (each at 25 μM) and 2.5 U GeneTaq (Trademark; manufactured by Nippon Gene Co., Ltd.) in mixture of a final reaction volume of 50 μL were subjected to the following PCR; one round of 95° C. for 5 minutes, 35 cycles of 94° C. for 30 seconds, 55° C. for 30 seconds and 72° C. for 60 seconds and a final round of 72° C. for 5 minutes.

5 μL of the resulting PCR product was subjected to 1.2% agarose electrophoresis; the PCR product was detected at an expected size and considered to be derived from the 5′-terminus of human placenta lactogen mRNA. Using T4 RNA polymerase, the PCR product was blunt ended and subcloned in plasmid pUC19 preliminarily treated by digestion with a restriction endonuclease Smal and subsequent dephosphorylation, for the determination of the nucleotide sequence. Consequently, it was verified that the resulting 5′-terminal sequence of the human placenta lactogen mRNA coincided with the sequence reported in Genomics, 4(4): pp.479-497 (1989) and in Biochem. Int., 16 (2): pp.287-292 (1988).

FIG. 7 shows an explanatory diagram depicting the 5′-terminal analysis results of human placenta lactogen mRNA, based on human placenta 5′ cDNA. As shown in FIG. 7 , the nucleotide sequences of 25 clones in total were determined; 20 of the clones were the full-length clone (SEQ ID NOS: 469 to 470) reported in the aforementioned reports. Thus, 80% of the resulting clones corresponded to the full-length clone. Among the remaining 5 clones, 4 of the clones were shorter by one nucleotide (SEQ ID NO: 471); and one of the clones was shorter by 8 nucleotides (SEQ ID NO: 472). The possibility is very high, compared with 5′RACE analysis involving the deletion of several tens of nucleotides in almost all of the resulting clones. Thus, the method according to the present invention was confirmed as a very excellent method for the determination of the nucleotide sequence of the 5′-terminus of mRNA. Additionally, it was confirmed from the results of the invention that a different transcription start (arrow 2 ) was present in the mRNA, other than the reported transcription start marked with arrow 1 .

EXAMPLE 6

Examination of Oligoribonucleotide

The individual oligoribonucleotides shown in Example 4 were examined by using the individual oligoribonucleotides in the reaction system shown in the step 3 of Example 5 to synthesize cDNA finally for subsequent comparison of the amplification degree of human placenta lactogen.

Under the same conditions as in Example 5 except for the modification of the oligonucleotide at the step 3, the reaction was promoted to prepare finally human placenta 5′ cDNA.

Using as template human placenta 5′ cDNA carrying the sequence from each of the oligoribonucleotides at the 5′-terminus and the primer ASP1 amplifying the placenta lactogen 5′ cDNA, synthesizing a primer capable of being annealed to the sequence derived from each of the individual oligoribonucleotides and appropriately diluting the human placenta 5′ cDNA, PCR was carried out for the comparison of the amplification degrees with the resulting individual primer sets.

PCR was carried out under the following conditions. 1 μL of template human placenta 5′ cDNA in 5-fold seiral dilutions, 2.5 μL of 10 GeneTaq buffer, 2.5 μL of 2.5 mM dNTP mixture solution, 0.5 μL each of ASP1 and each oligoribonucleotide-specific primer (each of 25 μM) and 2.5 U GeneTaq were mixed together to a final reaction volume of 25 μL; one round of 95° C. for 5 minutes and 35 cycles of 94° C. for 30 seconds, 55° C. for 30 seconds and 72° C. for 60 seconds were carried out, followed by a final round of 72° C. for 5 minutes. 5 μL of the resulting PCR product was subjected to 1.2% agarose electrophoresis; and the amplification degree was estimated. The oligoribonucleotide-specific primers used herein are shown below in Table 6. Herein, the sequences of the primers in Table 6 are listed as SQ ID Nos. 11 through 14, below, in the attached sequence listing table.

TABLE 6
RNA oligo	Primer sequences (5′-3′; name)
GG	GCGTTACACAGCGTATGATGCGT	(RC5′)
AA	GCGTTACACAGCGTATGATGCGT	(RC5′)
GU	GCGTTACACAGCGTATGATGCGT	(RC5′)
RC + GU	GTACGCCGTTGCGTTACACAGC	(1RC5′)
RC + AA	GTACGCCGTTGCGTTACACAGC	(1RC5′)
RC2 + GU	GCGTTACAAGGTACGCCACAGCGT	(1RC2)
RC2 + AA	GCGTTACAAGGTACGCCACAGCGT	(1RC2)
Vectorette	CGAATCGTAACCGTTCGTACGAG	(vectorette 1)

Step 1:

The sequences of RNA oligos, namely GG, M and GU, were compared to each other. The results by agarose gel electrophoresis indicate that AA is the most efficient at a ratio of GG:M:GU=1:3:4. It is deduced that the results reflect the reaction efficiency of T4 RNA ligase because the sequences of GG, AA and GU differ only in 3′-terminal sequence. Thus, the 3′-terminus of oligoribonucleotide was prepared with reference to the 3′-terminal sequence of AA or GU.

Step 2:

So as to prepare several primer-binding sites in the cDNA domain derived from each oligoribonucleotide by further elongating the oligoribonucleotide, “RC+GU” and “RC+M” were designed in longer lengths and compared with M and GU. Consequently, the amplification of the PCR product was most sensitively observed with “RC+GU”.

Step 3:

From the respect of PCR primer efficiency, other oligoribonucleotides RO1 and RO2 with less CG dinucleotide sequences and small homolog scores were synthesized from the respect of the presence of CpG island at 5′-terminus, together with “RC2+GU” and “RC2+AA” for the comparison of the amplification in different sequences with small homolog scores; additionally, a sequence designed on the basis of the sequence used in the vectorette method reported in Proc. Natl. Acad. Sci. USA, 91 (12): pp.5377-5381 (1994) was synthesized, for comparison. Furthermore, the two types of oligoribonucleotides, namely RO1 and RO2, are composed of the entirety or a part of a series of 10-base sequences (T was modified into U) with no CG dinucleotide sequence (B-19 (Table 4), H-11 (Table 5), E-05 (Table 4 ), B-33 (Table 2 ) and C-10 (Table 3)). These sequences are shown in detail as SQ ID Nos. 15 and 16 below in the attached sequence listing table.

FIG. 8 shows an explanatory diagram depicting the examination by PCR and electrophoresis of 5′-terminal cDNA from human placenta lactogen mRNA, as prepared by using various oligoribonucleotide sequences. As shown in the figure, a band about 600-bp was observed sharply in lanes 1, 2, 3 and 4. As indicated in lane 2, however, “RC2+M” the most efficiently amplified the 5′-terminus of placenta lactogen.

EXAMPLE 7

Analysis of Transferrin Receptor 5′ cDNA Based on Human Placenta Oligo Capping cDNA

In the analysis of the 5′ cDNA of human placenta lactogen insofar, the gene with a high expression level such that the expression of human placenta lactogen mRNA amounted to about 3% of all the mRNAs was used as subject. Then, the 5° cDNA of transferrin receptor mRNA was analyzed, of which the expression level is said to belong to medium level.

As a primer amplifying transferrin receptor 5′ cDNA, use was made of TFRA3 (5′-GCTTCACATTCTTGCTTTCTGAGG-3′) or TFRA4 (5′-GCTTGATGGTGCTGGTGAAGTCTG-3′) (McClelland, A., et al. Cell 39: pp.267-274 (1984)). The sequences of these primers TFRA3 and TFRA4 are shown as SQ ID Nos. 17 and 18 in the attached sequence listing table. These were subjected to the following PCR in a final reaction volume of 25 μL containing 1 μL of human placenta oligo capping cDNA, 2.5 μL of 10×GeneTaq buffer, 2.5 μL of 2.5 mM dNTP mixture solution, 0.5 μL each of TRFA4 and 1RC2 (each of 25 μM), and 2.5 U of GeneTaq; PCR was conducted at a round of 95° C. for 5 minutes and 35 cycles of procedures of 94° C. for 30 seconds, 55° C. for 30 seconds and 72° C. for 60 seconds and a final round of 72° C. for 5 minutes.

FIG. 9 shows an explanatory diagram of the PCR amplification results of the transferrin receptor 5′ cDNA, based on the human placenta oligo capping cDNA. In the figure, FIG. 9 a depicts the approximate expected sizes of the PCR products when two primes were used, namely TFRA3 and TFRA4; and FIG. 9 b schematically shows the electrophoresis results. 5 μL each of the resulting PCR products was subjected to 1.2% agarose electrophoresis. Consequently, a PCR product was detected at an estimated 530-bp size, when TRFA4 was used. This indicates that the product is derived from the 5′-terminus of human placenta transferrin receptor mRNA. However, no band was observed at an estimated 1200-bp size, when TRFA3 was used, which is indicated to be due to the length of the PCR product recovered by using the primer TRFA3, which is too long. So as to recover such PCR product, importantly, the primer is designed to generate a PCR product of about 300 to 500 bases.

The amplified product blunt ended by using T4 RNA polymerase was subcloned in plasmid pUC19 preliminarily digested with a restriction endonuclease Smal and treated with dephosphorylation, for the determination of the nucleotide sequence. As reported in Cell, 39: pp.267-274 (1984 ) and EMBO. J. 6: pp.1287-1293 (1987), it was indicated that the amplified product was the 5′-terminal sequence. Accordingly, it was confirmed that the human placenta oligo capping cDNA of the invention made a fewer copies of mRNA to be effective for the analysis of full-length 5′ cDNA of the gene. These results indicate that the inventive method can analyze the 5′ cDNA sequence at a very high probability, compared with conventional 5′ RACE.

The reason is as follows; according to 5′ RACE, PCR is conducted after reverse transcription and adapter attachment, so products recovered with no reverse transcription going up to the transcription start serve as subjects for PCR. In accordance with the present invention, principally, an oligoribonucleotide addition is effected using an enzyme specifically removing the cap structure of RNA, prior to reverse transcription; by PCR using a primer complementary to the oligoribonucleotide, only cDNA containing the transcription start adjacent to the cap structure is a PCR subject; and thus, 5′ cDNA can be analyzed at a very high probability (almost 100%).

472 1 30 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 1guugcguuac acagcguaug augcguaagg 30 2 28 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 2guugcguuac acagcguaug augcguaa 28 3 26 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 3guugcguuac acagcguaug augcgu 26 4 36 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 4aagguacgcc guugcguuac acagcguaug augcgu 36 5 38 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 5aagguacgcc guugcguuac acagcguaug augcguaa 38 6 36 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 6guugcguuac aagguacgcc acagcguaug augcgu 36 7 38 RNA Artificial Sequence Description of Artificial Sequence Oligonucleotide 7guugcguuac aagguacgcc acagcguaug augcguaa 38 8 30 RNA Artificial Sequence Description of Artificial Sequence Vectorette 8cgaaucguaa ccguucguac gagaaucgcu 30 9 24 DNA Artificial Sequence Description of Artificial Sequence Primer 9gttggagggt gtcggaatag agtc 24 10 23 DNA Artificial Sequence Description of Artificial Sequence Primer 10gcgttacaca gcgtatgatg cgt 23 11 22 DNA Artificial Sequence Description of Artificial Sequence Primer 11gtacgccgtt gcgttacaca gc 22 12 24 DNA Artificial Sequence Description of Artificial Sequence Primer 12gcgttacaag gtacgccaca gcgt 24 13 23 DNA Artificial Sequence Description of Artificial Sequence Primer 13gtcctatgtg atgaccagtg atg 23 14 23 DNA Artificial Sequence Description of Artificial Sequence Primer 14cgaatcgtaa ccgttcgtac gag 23 15 37 RNA Artificial Sequence Description of Artificial Sequence Oligoribonucleotide 15gaguccuaug cauaggacuc cugauacagc ugccagu 37 16 37 RNA Artificial Sequence Description of Artificial Sequence Oligoribonucleotide 16gaguccuaug ugaugaccag ugaugaccag ugccagu 37 17 24 DNA Artificial Sequence Description of Artificial Sequence Primer 17gcttcacatt cttgctttct gagg 24 18 24 DNA Artificial Sequence Description of Artificial Sequence Primer 18gcttgatggt gctggtgaag tctg 24 19 10 DNA Artificial Sequence Description of Artificial Sequence Primer 19ctggagaaac 10 20 10 DNA Artificial Sequence Description of Artificial Sequence Primer 20tctgaagagg 10 21 10 DNA Artificial Sequence Description of Artificial Sequence Primer 21tttctcctgc 10 22 10 DNA Artificial Sequence Description of Artificial Sequence Primer 22tgctggaaag 10 23 10 DNA Artificial Sequence Description of Artificial Sequence Primer 23tgcgggaaac 10 24 10 DNA Artificial Sequence Description of Artificial Sequence Primer 24agggaaaagg 10 25 10 DNA Artificial Sequence Description of Artificial Sequence Primer 25actgctgaag 10 26 10 DNA Artificial Sequence Description of Artificial Sequence Primer 26aacagaggag 10 27 10 DNA Artificial Sequence Description of Artificial Sequence Primer 27atcctcttcc 10 28 10 DNA Artificial Sequence Description of Artificial Sequence Primer 28acatcagcag 10 29 10 DNA Artificial Sequence Description of Artificial Sequence Primer 29gagaagagtg 10 30 10 DNA Artificial Sequence Description of Artificial Sequence Primer 30gagaaacagg 10 31 10 DNA Artificial Sequence Description of Artificial Sequence Primer 31actgaggatg 10 32 10 DNA Artificial Sequence Description of Artificial Sequence Primer 32acaaaggagg 10 33 10 DNA Artificial Sequence Description of Artificial Sequence Primer 33aggaagacag 10 34 10 DNA Artificial Sequence Description of Artificial Sequence Primer 34gacaaggatg 10 35 10 DNA Artificial Sequence Description of Artificial Sequence Primer 35tgaggaaagc 10 36 10 DNA Artificial Sequence Description of Artificial Sequence Primer 36ttctgcttcc 10 37 10 DNA Artificial Sequence Description of Artificial Sequence Primer 37ggaaaagcag 10 38 10 DNA Artificial Sequence Description of Artificial Sequence Primer 38ggacagaaag 10 39 10 DNA Artificial Sequence Description of Artificial Sequence Primer 39agaccatctc 10 40 10 DNA Artificial Sequence Description of Artificial Sequence Primer 40gtgacagaag 10 41 10 DNA Artificial Sequence Description of Artificial Sequence Primer 41gtttctccag 10 42 10 DNA Artificial Sequence Description of Artificial Sequence Primer 42acaacaaggc 10 43 10 DNA Artificial Sequence Description of Artificial Sequence Primer 43gtggtgaaag 10 44 10 DNA Artificial Sequence Description of Artificial Sequence Primer 44ttcctttccc 10 45 10 DNA Artificial Sequence Description of Artificial Sequence Primer 45tttcctcacc 10 46 10 DNA Artificial Sequence Description of Artificial Sequence Primer 46accaccaaag 10 47 10 DNA Artificial Sequence Description of Artificial Sequence Primer 47aatccagcag 10 48 10 DNA Artificial Sequence Description of Artificial Sequence Primer 48gaaagagctg 10 49 10 DNA Artificial Sequence Description of Artificial Sequence Primer 49ttctgtggac 10 50 10 DNA Artificial Sequence Description of Artificial Sequence Primer 50aaaaggcagg 10 51 10 DNA Artificial Sequence Description of Artificial Sequence Primer 51caccagaaac 10 52 10 DNA Artificial Sequence Description of Artificial Sequence Primer 52tgaggtgaac 10 53 10 DNA Artificial Sequence Description of Artificial Sequence Primer 53ctcctgaaac 10 54 10 DNA Artificial Sequence Description of Artificial Sequence Primer 54ttctcaggag 10 55 10 DNA Artificial Sequence Description of Artificial Sequence Primer 55cctgaaactg 10 56 10 DNA Artificial Sequence Description of Artificial Sequence Primer 56atctgggaac 10 57 10 DNA Artificial Sequence Description of Artificial Sequence Primer 57cagaaagacg 10 58 10 DNA Artificial Sequence Description of Artificial Sequence Primer 58actccttcag 10 59 10 DNA Artificial Sequence Description of Artificial Sequence Primer 59tgaaaccagc 10 60 10 DNA Artificial Sequence Description of Artificial Sequence Primer 60tgtctttgcc 10 61 10 DNA Artificial Sequence Description of Artificial Sequence Primer 61caatgctgag 10 62 10 DNA Artificial Sequence Description of Artificial Sequence Primer 62tgagagatgg 10 63 10 DNA Artificial Sequence Description of Artificial Sequence Primer 63tggtgaagtc 10 64 10 DNA Artificial Sequence Description of Artificial Sequence Primer 64cctgtttctc 10 65 10 DNA Artificial Sequence Description of Artificial Sequence Primer 65tcagcaactg 10 66 10 DNA Artificial Sequence Description of Artificial Sequence Primer 66ccgaaagaag 10 67 10 DNA Artificial Sequence Description of Artificial Sequence Primer 67gaggtgaatg 10 68 10 DNA Artificial Sequence Description of Artificial Sequence Primer 68gtcatcaagc 10 69 10 DNA Artificial Sequence Description of Artificial Sequence Primer 69tgttttcccc 10 70 10 DNA Artificial Sequence Description of Artificial Sequence Primer 70atttctgccc 10 71 10 DNA Artificial Sequence Description of Artificial Sequence Primer 71cagctctttc 10 72 10 DNA Artificial Sequence Description of Artificial Sequence Primer 72aaaccacagc 10 73 10 DNA Artificial Sequence Description of Artificial Sequence Primer 73cactcttctc 10 74 10 DNA Artificial Sequence Description of Artificial Sequence Primer 74ctttctgtcc 10 75 10 DNA Artificial Sequence Description of Artificial Sequence Primer 75cgaaaaccag 10 76 10 DNA Artificial Sequence Description of Artificial Sequence Primer 76ctgcttttcc 10 77 10 DNA Artificial Sequence Description of Artificial Sequence Primer 77gaatgaagcc 10 78 10 DNA Artificial Sequence Description of Artificial Sequence Primer 78ttgctgagtg 10 79 10 DNA Artificial Sequence Description of Artificial Sequence Primer 79gtttctggtg 10 80 10 DNA Artificial Sequence Description of Artificial Sequence Primer 80gaccaaagac 10 81 10 DNA Artificial Sequence Description of Artificial Sequence Primer 81attcctgtgg 10 82 10 DNA Artificial Sequence Description of Artificial Sequence Primer 82gagacacaac 10 83 10 DNA Artificial Sequence Description of Artificial Sequence Primer 83cccaaaacac 10 84 10 DNA Artificial Sequence Description of Artificial Sequence Primer 84gtgtttgtgc 10 85 10 DNA Artificial Sequence Description of Artificial Sequence Primer 85tttgctccag 10 86 10 DNA Artificial Sequence Description of Artificial Sequence Primer 86ctgatgacag 10 87 10 DNA Artificial Sequence Description of Artificial Sequence Primer 87ttcagaggtg 10 88 10 DNA Artificial Sequence Description of Artificial Sequence Primer 88aaaggtgagc 10 89 10 DNA Artificial Sequence Description of Artificial Sequence Primer 89atcacacacc 10 90 10 DNA Artificial Sequence Description of Artificial Sequence Primer 90gaatgccaac 10 91 10 DNA Artificial Sequence Description of Artificial Sequence Primer 91cagtgatgac 10 92 10 DNA Artificial Sequence Description of Artificial Sequence Primer 92gtgacttctg 10 93 10 DNA Artificial Sequence Description of Artificial Sequence Primer 93tgctgaacag 10 94 10 DNA Artificial Sequence Description of Artificial Sequence Primer 94gtttcaggag 10 95 10 DNA Artificial Sequence Description of Artificial Sequence Primer 95tgtcatcagc 10 96 10 DNA Artificial Sequence Description of Artificial Sequence Primer 96acacaggaac 10 97 10 DNA Artificial Sequence Description of Artificial Sequence Primer 97tcatctgctc 10 98 10 DNA Artificial Sequence Description of Artificial Sequence Primer 98aaagcagacg 10 99 10 DNA Artificial Sequence Description of Artificial Sequence Primer 99aagtcagagg 10 100 10 DNA Artificial Sequence Description of Artificial Sequence Primer 100caaatgccac 10 101 10 DNA Artificial Sequence Description of Artificial Sequence Primer 101tgagagtgag 10 102 10 DNA Artificial Sequence Description of Artificial Sequence Primer 102aatgccaacc 10 103 10 DNA Artificial Sequence Description of Artificial Sequence Primer 103tgtggagttc 10 104 10 DNA Artificial Sequence Description of Artificial Sequence Primer 104cagaagtcac 10 105 10 DNA Artificial Sequence Description of Artificial Sequence Primer 105ttttctgccg 10 106 10 DNA Artificial Sequence Description of Artificial Sequence Primer 106aatctgctcc 10 107 10 DNA Artificial Sequence Description of Artificial Sequence Primer 107atccagttcc 10 108 10 DNA Artificial Sequence Description of Artificial Sequence Primer 108gcacaaacac 10 109 10 DNA Artificial Sequence Description of Artificial Sequence Primer 109tcacaccaac 10 110 10 DNA Artificial Sequence Description of Artificial Sequence Primer 110cgtctttctg 10 111 10 DNA Artificial Sequence Description of Artificial Sequence Primer 111ctgtcatcag 10 112 10 DNA Artificial Sequence Description of Artificial Sequence Primer 112ctttcaccac 10 113 10 DNA Artificial Sequence Description of Artificial Sequence Primer 113tgatgaccag 10 114 10 DNA Artificial Sequence Description of Artificial Sequence Primer 114gcaaatggtg 10 115 10 DNA Artificial Sequence Description of Artificial Sequence Primer 115gtgttttggg 10 116 10 DNA Artificial Sequence Description of Artificial Sequence Primer 116cttctgtcac 10 117 10 DNA Artificial Sequence Description of Artificial Sequence Primer 117atggctgaac 10 118 10 DNA Artificial Sequence Description of Artificial Sequence Primer 118acaaggtcac 10 119 10 DNA Artificial Sequence Description of Artificial Sequence Primer 119gagcagattg 10 120 10 DNA Artificial Sequence Description of Artificial Sequence Primer 120gtcatcactg 10 121 10 DNA Artificial Sequence Description of Artificial Sequence Primer 121gattcagagc 10 122 10 DNA Artificial Sequence Description of Artificial Sequence Primer 122tcagaccatc 10 123 10 DNA Artificial Sequence Description of Artificial Sequence Primer 123gattcagagg 10 124 10 DNA Artificial Sequence Description of Artificial Sequence Primer 124aatgccagag 10 125 10 DNA Artificial Sequence Description of Artificial Sequence Primer 125ggaactgaag 10 126 10 DNA Artificial Sequence Description of Artificial Sequence Primer 126gaaactgagc 10 127 10 DNA Artificial Sequence Description of Artificial Sequence Primer 127tctggttctc 10 128 10 DNA Artificial Sequence Description of Artificial Sequence Primer 128aaaaaggggc 10 129 10 DNA Artificial Sequence Description of Artificial Sequence Primer 129accagtttcc 10 130 10 DNA Artificial Sequence Description of Artificial Sequence Primer 130catcaaccag 10 131 10 DNA Artificial Sequence Description of Artificial Sequence Primer 131gctcagtttc 10 132 10 DNA Artificial Sequence Description of Artificial Sequence Primer 132tggatgaacg 10 133 10 DNA Artificial Sequence Description of Artificial Sequence Primer 133tttctctcgg 10 134 10 DNA Artificial Sequence Description of Artificial Sequence Primer 134gctctgaatc 10 135 10 DNA Artificial Sequence Description of Artificial Sequence Primer 135actttctccg 10 136 10 DNA Artificial Sequence Description of Artificial Sequence Primer 136ttcaccagtg 10 137 10 DNA Artificial Sequence Description of Artificial Sequence Primer 137ctgctcaaac 10 138 10 DNA Artificial Sequence Description of Artificial Sequence Primer 138attgctcagg 10 139 10 DNA Artificial Sequence Description of Artificial Sequence Primer 139agttctgctc 10 140 10 DNA Artificial Sequence Description of Artificial Sequence Primer 140cggaaaagtc 10 141 10 DNA Artificial Sequence Description of Artificial Sequence Primer 141ttttggctcc 10 142 10 DNA Artificial Sequence Description of Artificial Sequence Primer 142cagtttcagg 10 143 10 DNA Artificial Sequence Description of Artificial Sequence Primer 143gtctttggtc 10 144 10 DNA Artificial Sequence Description of Artificial Sequence Primer 144gaaagagtgg 10 145 10 DNA Artificial Sequence Description of Artificial Sequence Primer 145ggtgaacaac 10 146 10 DNA Artificial Sequence Description of Artificial Sequence Primer 146gatctcagac 10 147 10 DNA Artificial Sequence Description of Artificial Sequence Primer 147ctacaatgcc 10 148 10 DNA Artificial Sequence Description of Artificial Sequence Primer 148cgtgtttgag 10 149 10 DNA Artificial Sequence Description of Artificial Sequence Primer 149cctctgaatc 10 150 10 DNA Artificial Sequence Description of Artificial Sequence Primer 150caaactcacc 10 151 10 DNA Artificial Sequence Description of Artificial Sequence Primer 151tccctgtttg 10 152 10 DNA Artificial Sequence Description of Artificial Sequence Primer 152aacatctggc 10 153 10 DNA Artificial Sequence Description of Artificial Sequence Primer 153cttcagttcc 10 154 10 DNA Artificial Sequence Description of Artificial Sequence Primer 154ggcttcattc 10 155 10 DNA Artificial Sequence Description of Artificial Sequence Primer 155tcaaacaggg 10 156 10 DNA Artificial Sequence Description of Artificial Sequence Primer 156aaacaccacg 10 157 10 DNA Artificial Sequence Description of Artificial Sequence Primer 157gttgtgtctc 10 158 10 DNA Artificial Sequence Description of Artificial Sequence Primer 158aatcagccac 10 159 10 DNA Artificial Sequence Description of Artificial Sequence Primer 159ctcagcattg 10 160 10 DNA Artificial Sequence Description of Artificial Sequence Primer 160actgaactcc 10 161 10 DNA Artificial Sequence Description of Artificial Sequence Primer 161actgagatcc 10 162 10 DNA Artificial Sequence Description of Artificial Sequence Primer 162tctttgctcg 10 163 10 DNA Artificial Sequence Description of Artificial Sequence Primer 163agggcaaaac 10 164 10 DNA Artificial Sequence Description of Artificial Sequence Primer 164tgaactggtc 10 165 10 DNA Artificial Sequence Description of Artificial Sequence Primer 165ctttctaccc 10 166 10 DNA Artificial Sequence Description of Artificial Sequence Primer 166taagccatcc 10 167 10 DNA Artificial Sequence Description of Artificial Sequence Primer 167ctggttttcg 10 168 10 DNA Artificial Sequence Description of Artificial Sequence Primer 168ttgccacttc 10 169 10 DNA Artificial Sequence Description of Artificial Sequence Primer 169ttgttcccag 10 170 10 DNA Artificial Sequence Description of Artificial Sequence Primer 170gtgaatggtg 10 171 10 DNA Artificial Sequence Description of Artificial Sequence Primer 171tggattggtc 10 172 10 DNA Artificial Sequence Description of Artificial Sequence Primer 172acagaggttc 10 173 10 DNA Artificial Sequence Description of Artificial Sequence Primer 173ccacaaatcc 10 174 10 DNA Artificial Sequence Description of Artificial Sequence Primer 174agtcctgaac 10 175 10 DNA Artificial Sequence Description of Artificial Sequence Primer 175ggtgagtttg 10 176 10 DNA Artificial Sequence Description of Artificial Sequence Primer 176actgacacag 10 177 10 DNA Artificial Sequence Description of Artificial Sequence Primer 177gtgagttcac 10 178 10 DNA Artificial Sequence Description of Artificial Sequence Primer 178tctggtttcg 10 179 10 DNA Artificial Sequence Description of Artificial Sequence Primer 179tttgtgccac 10 180 10 DNA Artificial Sequence Description of Artificial Sequence Primer 180gtgaactcac 10 181 10 DNA Artificial Sequence Description of Artificial Sequence Primer 181aacacatccg 10 182 10 DNA Artificial Sequence Description of Artificial Sequence Primer 182gtacaagtcc 10 183 10 DNA Artificial Sequence Description of Artificial Sequence Primer 183aggtggtttc 10 184 10 DNA Artificial Sequence Description of Artificial Sequence Primer 184agccattctg 10 185 10 DNA Artificial Sequence Description of Artificial Sequence Primer 185ggatttgtgg 10 186 10 DNA Artificial Sequence Description of Artificial Sequence Primer 186tgaacacacc 10 187 10 DNA Artificial Sequence Description of Artificial Sequence Primer 187aagagtggtg 10 188 10 DNA Artificial Sequence Description of Artificial Sequence Primer 188cattcacctc 10 189 10 DNA Artificial Sequence Description of Artificial Sequence Primer 189tggctgattg 10 190 10 DNA Artificial Sequence Description of Artificial Sequence Primer 190ccactctttc 10 191 10 DNA Artificial Sequence Description of Artificial Sequence Primer 191tgaactgtgc 10 192 10 DNA Artificial Sequence Description of Artificial Sequence Primer 192gcttgatgac 10 193 10 DNA Artificial Sequence Description of Artificial Sequence Primer 193gtggcatttg 10 194 10 DNA Artificial Sequence Description of Artificial Sequence Primer 194tgctcagttg 10 195 10 DNA Artificial Sequence Description of Artificial Sequence Primer 195ggattcactg 10 196 10 DNA Artificial Sequence Description of Artificial Sequence Primer 196tgaaatgccc 10 197 10 DNA Artificial Sequence Description of Artificial Sequence Primer 197aaacaggtgc 10 198 10 DNA Artificial Sequence Description of Artificial Sequence Primer 198cgctgaaatc 10 199 10 DNA Artificial Sequence Description of Artificial Sequence Primer 199ctgattcagg 10 200 10 DNA Artificial Sequence Description of Artificial Sequence Primer 200tggttttgcg 10 201 10 DNA Artificial Sequence Description of Artificial Sequence Primer 201gtttgagcag 10 202 10 DNA Artificial Sequence Description of Artificial Sequence Primer 202aaagtgccac 10 203 10 DNA Artificial Sequence Description of Artificial Sequence Primer 203acattggcag 10 204 10 DNA Artificial Sequence Description of Artificial Sequence Primer 204cttctttcgg 10 205 10 DNA Artificial Sequence Description of Artificial Sequence Primer 205caccatttgc 10 206 10 DNA Artificial Sequence Description of Artificial Sequence Primer 206gatcatggtc 10 207 10 DNA Artificial Sequence Description of Artificial Sequence Primer 207cacctgatac 10 208 10 DNA Artificial Sequence Description of Artificial Sequence Primer 208cacttttccg 10 209 10 DNA Artificial Sequence Description of Artificial Sequence Primer 209catccttgtc 10 210 10 DNA Artificial Sequence Description of Artificial Sequence Primer 210caccattcac 10 211 10 DNA Artificial Sequence Description of Artificial Sequence Primer 211gtaatggtgg 10 212 10 DNA Artificial Sequence Description of Artificial Sequence Primer 212agccagtttc 10 213 10 DNA Artificial Sequence Description of Artificial Sequence Primer 213acagtgctac 10 214 10 DNA Artificial Sequence Description of Artificial Sequence Primer 214caatctgctc 10 215 10 DNA Artificial Sequence Description of Artificial Sequence Primer 215aatgacagcg 10 216 10 DNA Artificial Sequence Description of Artificial Sequence Primer 216tactgttgcc 10 217 10 DNA Artificial Sequence Description of Artificial Sequence Primer 217ggaactacag 10 218 10 DNA Artificial Sequence Description of Artificial Sequence Primer 218tgaacaggtg 10 219 10 DNA Artificial Sequence Description of Artificial Sequence Primer 219acttttggcg 10 220 10 DNA Artificial Sequence Description of Artificial Sequence Primer 220atttctgcgg 10 221 10 DNA Artificial Sequence Description of Artificial Sequence Primer 221tcaacatcgc 10 222 10 DNA Artificial Sequence Description of Artificial Sequence Primer 222agcacaatgg 10 223 10 DNA Artificial Sequence Description of Artificial Sequence Primer 223ggaaccaatc 10 224 10 DNA Artificial Sequence Description of Artificial Sequence Primer 224tgcctcattg 10 225 10 DNA Artificial Sequence Description of Artificial Sequence Primer 225tcttgagcag 10 226 10 DNA Artificial Sequence Description of Artificial Sequence Primer 226aaaggcatcg 10 227 10 DNA Artificial Sequence Description of Artificial Sequence Primer 227aggcaaactg 10 228 10 DNA Artificial Sequence Description of Artificial Sequence Primer 228ctcaaacacg 10 229 10 DNA Artificial Sequence Description of Artificial Sequence Primer 229acctttcacc 10 230 10 DNA Artificial Sequence Description of Artificial Sequence Primer 230gaaactcacg 10 231 10 DNA Artificial Sequence Description of Artificial Sequence Primer 231gatttcagcg 10 232 10 DNA Artificial Sequence Description of Artificial Sequence Primer 232gttggcattc 10 233 10 DNA Artificial Sequence Description of Artificial Sequence Primer 233ttttctgcgg 10 234 10 DNA Artificial Sequence Description of Artificial Sequence Primer 234catctgactg 10 235 10 DNA Artificial Sequence Description of Artificial Sequence Primer 235ttggctgtac 10 236 10 DNA Artificial Sequence Description of Artificial Sequence Primer 236ccgtgaaaag 10 237 10 DNA Artificial Sequence Description of Artificial Sequence Primer 237gcagattgtc 10 238 10 DNA Artificial Sequence Description of Artificial Sequence Primer 238ttgcaggttg 10 239 10 DNA Artificial Sequence Description of Artificial Sequence Primer 239ccagattgtc 10 240 10 DNA Artificial Sequence Description of Artificial Sequence Primer 240ctggttgatg 10 241 10 DNA Artificial Sequence Description of Artificial Sequence Primer 241ccaccattac 10 242 10 DNA Artificial Sequence Description of Artificial Sequence Primer 242agtgacatcg 10 243 10 DNA Artificial Sequence Description of Artificial Sequence Primer 243aatctcaccc 10 244 10 DNA Artificial Sequence Description of Artificial Sequence Primer 244atttcagccg 10 245 10 DNA Artificial Sequence Description of Artificial Sequence Primer 245ctatccagtc 10 246 10 DNA Artificial Sequence Description of Artificial Sequence Primer 246tgaggtttgc 10 247 10 DNA Artificial Sequence Description of Artificial Sequence Primer 247gatgagttcg 10 248 10 DNA Artificial Sequence Description of Artificial Sequence Primer 248cttacctgac 10 249 10 DNA Artificial Sequence Description of Artificial Sequence Primer 249gttgttcacc 10 250 10 DNA Artificial Sequence Description of Artificial Sequence Primer 250atacacccac 10 251 10 DNA Artificial Sequence Description of Artificial Sequence Primer 251gtatcaggag 10 252 10 DNA Artificial Sequence Description of Artificial Sequence Primer 252cagtggtatg 10 253 10 DNA Artificial Sequence Description of Artificial Sequence Primer 253cctgaatcag 10 254 10 DNA Artificial Sequence Description of Artificial Sequence Primer 254tgacagtcac 10 255 10 DNA Artificial Sequence Description of Artificial Sequence Primer 255gactggatag 10 256 10 DNA Artificial Sequence Description of Artificial Sequence Primer 256tttgtcaccg 10 257 10 DNA Artificial Sequence Description of Artificial Sequence Primer 257aatggtctgc 10 258 10 DNA Artificial Sequence Description of Artificial Sequence Primer 258aaaagacccg 10 259 10 DNA Artificial Sequence Description of Artificial Sequence Primer 259tggtaaaggg 10 260 10 DNA Artificial Sequence Description of Artificial Sequence Primer 260cattaccagc 10 261 10 DNA Artificial Sequence Description of Artificial Sequence Primer 261gatctgacac 10 262 10 DNA Artificial Sequence Description of Artificial Sequence Primer 262ttcattcccg 10 263 10 DNA Artificial Sequence Description of Artificial Sequence Primer 263cattactgcg 10 264 10 DNA Artificial Sequence Description of Artificial Sequence Primer 264ctacaagtcc 10 265 10 DNA Artificial Sequence Description of Artificial Sequence Primer 265cataccactg 10 266 10 DNA Artificial Sequence Description of Artificial Sequence Primer 266tcaccctttg 10 267 10 DNA Artificial Sequence Description of Artificial Sequence Primer 267tttgagcacg 10 268 10 DNA Artificial Sequence Description of Artificial Sequence Primer 268aaacctgtcg 10 269 10 DNA Artificial Sequence Description of Artificial Sequence Primer 269gtaccagtac 10 270 10 DNA Artificial Sequence Description of Artificial Sequence Primer 270gacaatctgg 10 271 10 DNA Artificial Sequence Description of Artificial Sequence Primer 271gctgtatcag 10 272 10 DNA Artificial Sequence Description of Artificial Sequence Primer 272cgtgagtttc 10 273 10 DNA Artificial Sequence Description of Artificial Sequence Primer 273tgccagtatg 10 274 10 DNA Artificial Sequence Description of Artificial Sequence Primer 274ggcattgtag 10 275 10 DNA Artificial Sequence Description of Artificial Sequence Primer 275gtcaggtaag 10 276 10 DNA Artificial Sequence Description of Artificial Sequence Primer 276gcaagtgtag 10 277 10 DNA Artificial Sequence Description of Artificial Sequence Primer 277gtcctgatac 10 278 10 DNA Artificial Sequence Description of Artificial Sequence Primer 278cataccagac 10 279 10 DNA Artificial Sequence Description of Artificial Sequence Primer 279tttcacaccg 10 280 10 DNA Artificial Sequence Description of Artificial Sequence Primer 280ctgcttgatg 10 281 10 DNA Artificial Sequence Description of Artificial Sequence Primer 281gacaatctgc 10 282 10 DNA Artificial Sequence Description of Artificial Sequence Primer 282cgaactcatc 10 283 10 DNA Artificial Sequence Description of Artificial Sequence Primer 283tacaacgagg 10 284 10 DNA Artificial Sequence Description of Artificial Sequence Primer 284gtatcaggac 10 285 10 DNA Artificial Sequence Description of Artificial Sequence Primer 285gcgtttgatg 10 286 10 DNA Artificial Sequence Description of Artificial Sequence Primer 286gctggtaatg 10 287 10 DNA Artificial Sequence Description of Artificial Sequence Primer 287cagtatcagc 10 288 10 DNA Artificial Sequence Description of Artificial Sequence Primer 288gaaaatccgc 10 289 10 DNA Artificial Sequence Description of Artificial Sequence Primer 289cagtgaatcc 10 290 10 DNA Artificial Sequence Description of Artificial Sequence Primer 290tgaaagtccg 10 291 10 DNA Artificial Sequence Description of Artificial Sequence Primer 291aaatggacgc 10 292 10 DNA Artificial Sequence Description of Artificial Sequence Primer 292agcagatacg 10 293 10 DNA Artificial Sequence Description of Artificial Sequence Primer 293ttatcccctg 10 294 10 DNA Artificial Sequence Description of Artificial Sequence Primer 294cagtatggtg 10 295 10 DNA Artificial Sequence Description of Artificial Sequence Primer 295tcagattgcg 10 296 10 DNA Artificial Sequence Description of Artificial Sequence Primer 296gcttacttcc 10 297 10 DNA Artificial Sequence Description of Artificial Sequence Primer 297cactaaaggg 10 298 10 DNA Artificial Sequence Description of Artificial Sequence Primer 298gctcagtatc 10 299 10 DNA Artificial Sequence Description of Artificial Sequence Primer 299tatgtgagcg 10 300 10 DNA Artificial Sequence Description of Artificial Sequence Primer 300tcgcatcaac 10 301 10 DNA Artificial Sequence Description of Artificial Sequence Primer 301gatactgagc 10 302 10 DNA Artificial Sequence Description of Artificial Sequence Primer 302ctacacttgc 10 303 10 DNA Artificial Sequence Description of Artificial Sequence Primer 303gtctggtatg 10 304 10 DNA Artificial Sequence Description of Artificial Sequence Primer 304gcggattttc 10 305 10 DNA Artificial Sequence Description of Artificial Sequence Primer 305gtttacctcc 10 306 10 DNA Artificial Sequence Description of Artificial Sequence Primer 306aggggaatac 10 307 10 DNA Artificial Sequence Description of Artificial Sequence Primer 307ctgatacagc 10 308 10 DNA Artificial Sequence Description of Artificial Sequence Primer 308catcaaacgc 10 309 10 DNA Artificial Sequence Description of Artificial Sequence Primer 309attcgtggag 10 310 10 DNA Artificial Sequence Description of Artificial Sequence Primer 310cttttcacgg 10 311 10 DNA Artificial Sequence Description of Artificial Sequence Primer 311cgtaaagcac 10 312 10 DNA Artificial Sequence Description of Artificial Sequence Primer 312ggaggtaaac 10 313 10 DNA Artificial Sequence Description of Artificial Sequence Primer 313cggagtttac 10 314 10 DNA Artificial Sequence Description of Artificial Sequence Primer 314acttgtcacg 10 315 10 DNA Artificial Sequence Description of Artificial Sequence Primer 315aacgagagag 10 316 10 DNA Artificial Sequence Description of Artificial Sequence Primer 316tgactgttcg 10 317 10 DNA Artificial Sequence Description of Artificial Sequence Primer 317cccctatttg 10 318 10 DNA Artificial Sequence Description of Artificial Sequence Primer 318atgactaccg 10 319 10 DNA Artificial Sequence Description of Artificial Sequence Primer 319actgtttcgg 10 320 10 DNA Artificial Sequence Description of Artificial Sequence Primer 320tgacggcaac 10 321 10 DNA Artificial Sequence Description of Artificial Sequence Primer 321aggtaaagcg 10 322 10 DNA Artificial Sequence Description of Artificial Sequence Primer 322ggctattctc 10 323 10 DNA Artificial Sequence Description of Artificial Sequence Primer 323gaaaacgtgg 10 324 10 DNA Artificial Sequence Description of Artificial Sequence Primer 324tttatggggc 10 325 10 DNA Artificial Sequence Description of Artificial Sequence Primer 325tagttgcctg 10 326 10 DNA Artificial Sequence Description of Artificial Sequence Primer 326tcggatttgc 10 327 10 DNA Artificial Sequence Description of Artificial Sequence Primer 327agtgggttac 10 328 10 DNA Artificial Sequence Description of Artificial Sequence Primer 328gctgatactg 10 329 10 DNA Artificial Sequence Description of Artificial Sequence Primer 329tttcaccgtg 10 330 10 DNA Artificial Sequence Description of Artificial Sequence Primer 330ggacttgtag 10 331 10 DNA Artificial Sequence Description of Artificial Sequence Primer 331tctgacgatg 10 332 10 DNA Artificial Sequence Description of Artificial Sequence Primer 332caaaaacggg 10 333 10 DNA Artificial Sequence Description of Artificial Sequence Primer 333agtgtaaggg 10 334 10 DNA Artificial Sequence Description of Artificial Sequence Primer 334gtaaactccg 10 335 10 DNA Artificial Sequence Description of Artificial Sequence Primer 335gtgccttatc 10 336 10 DNA Artificial Sequence Description of Artificial Sequence Primer 336accctatctc 10 337 10 DNA Artificial Sequence Description of Artificial Sequence Primer 337tgtaatccgc 10 338 10 DNA Artificial Sequence Description of Artificial Sequence Primer 338cactaacacc 10 339 10 DNA Artificial Sequence Description of Artificial Sequence Primer 339ccactatctg 10 340 10 DNA Artificial Sequence Description of Artificial Sequence Primer 340ggagtttacg 10 341 10 DNA Artificial Sequence Description of Artificial Sequence Primer 341gtgctttacg 10 342 10 DNA Artificial Sequence Description of Artificial Sequence Primer 342caccatactg 10 343 10 DNA Artificial Sequence Description of Artificial Sequence Primer 343gaaacgatgg 10 344 10 DNA Artificial Sequence Description of Artificial Sequence Primer 344atttggtcgg 10 345 10 DNA Artificial Sequence Description of Artificial Sequence Primer 345cagatagtgg 10 346 10 DNA Artificial Sequence Description of Artificial Sequence Primer 346agtgcttacc 10 347 10 DNA Artificial Sequence Description of Artificial Sequence Primer 347cacggaaatg 10 348 10 DNA Artificial Sequence Description of Artificial Sequence Primer 348ttcggtgatg 10 349 10 DNA Artificial Sequence Description of Artificial Sequence Primer 349gataaggcac 10 350 10 DNA Artificial Sequence Description of Artificial Sequence Primer 350ctgtagttcc 10 351 10 DNA Artificial Sequence Description of Artificial Sequence Primer 351ccacgttttc 10 352 10 DNA Artificial Sequence Description of Artificial Sequence Primer 352tgattggtcg 10 353 10 DNA Artificial Sequence Description of Artificial Sequence Primer 353ggtgttagtg 10 354 10 DNA Artificial Sequence Description of Artificial Sequence Primer 354catcgtgttg 10 355 10 DNA Artificial Sequence Description of Artificial Sequence Primer 355cgtaaactcc 10 356 10 DNA Artificial Sequence Description of Artificial Sequence Primer 356ccctttagtg 10 357 10 DNA Artificial Sequence Description of Artificial Sequence Primer 357cgcagtaatg 10 358 10 DNA Artificial Sequence Description of Artificial Sequence Primer 358gcagattacg 10 359 10 DNA Artificial Sequence Description of Artificial Sequence Primer 359cccgtttttg 10 360 10 DNA Artificial Sequence Description of Artificial Sequence Primer 360caaaacgctg 10 361 10 DNA Artificial Sequence Description of Artificial Sequence Primer 361gctcaatacg 10 362 10 DNA Artificial Sequence Description of Artificial Sequence Primer 362ttcgctgatg 10 363 10 DNA Artificial Sequence Description of Artificial Sequence Primer 363ttagcatccg 10 364 10 DNA Artificial Sequence Description of Artificial Sequence Primer 364tatcgctgtc 10 365 10 DNA Artificial Sequence Description of Artificial Sequence Primer 365acgggtaaag 10 366 10 DNA Artificial Sequence Description of Artificial Sequence Primer 366tacaccgaac 10 367 10 DNA Artificial Sequence Description of Artificial Sequence Primer 367gagaatagcc 10 368 10 DNA Artificial Sequence Description of Artificial Sequence Primer 368actaatgggc 10 369 10 DNA Artificial Sequence Description of Artificial Sequence Primer 369aatagcctcc 10 370 10 DNA Artificial Sequence Description of Artificial Sequence Primer 370cctaatcagc 10 371 10 DNA Artificial Sequence Description of Artificial Sequence Primer 371gtgataaccg 10 372 10 DNA Artificial Sequence Description of Artificial Sequence Primer 372gatctaaggc 10 373 10 DNA Artificial Sequence Description of Artificial Sequence Primer 373gagtcctatg 10 374 10 DNA Artificial Sequence Description of Artificial Sequence Primer 374aaactccgtc 10 375 10 DNA Artificial Sequence Description of Artificial Sequence Primer 375cgtattgagc 10 376 10 DNA Artificial Sequence Description of Artificial Sequence Primer 376agtcaacgtc 10 377 10 DNA Artificial Sequence Description of Artificial Sequence Primer 377gctgattagg 10 378 10 DNA Artificial Sequence Description of Artificial Sequence Primer 378caaatagggg 10 379 10 DNA Artificial Sequence Description of Artificial Sequence Primer 379agccgaaatg 10 380 10 DNA Artificial Sequence Description of Artificial Sequence Primer 380cgttatgagc 10 381 10 DNA Artificial Sequence Description of Artificial Sequence Primer 381gatcatagcc 10 382 10 DNA Artificial Sequence Description of Artificial Sequence Primer 382tttttccgcc 10 383 10 DNA Artificial Sequence Description of Artificial Sequence Primer 383cgtaatctgc 10 384 10 DNA Artificial Sequence Description of Artificial Sequence Primer 384actgataccg 10 385 10 DNA Artificial Sequence Description of Artificial Sequence Primer 385tttctgcgtc 10 386 10 DNA Artificial Sequence Description of Artificial Sequence Primer 386catttccgtg 10 387 10 DNA Artificial Sequence Description of Artificial Sequence Primer 387cagcgatttc 10 388 10 DNA Artificial Sequence Description of Artificial Sequence Primer 388cggttatcac 10 389 10 DNA Artificial Sequence Description of Artificial Sequence Primer 389gaaatcgctg 10 390 10 DNA Artificial Sequence Description of Artificial Sequence Primer 390tattgagcgg 10 391 10 DNA Artificial Sequence Description of Artificial Sequence Primer 391atgaacggtg 10 392 10 DNA Artificial Sequence Description of Artificial Sequence Primer 392atgaagcgac 10 393 10 DNA Artificial Sequence Description of Artificial Sequence Primer 393ggtactaagg 10 394 10 DNA Artificial Sequence Description of Artificial Sequence Primer 394agtgcgaaag 10 395 10 DNA Artificial Sequence Description of Artificial Sequence Primer 395cataggactc 10 396 10 DNA Artificial Sequence Description of Artificial Sequence Primer 396gtatgacgac 10 397 10 DNA Artificial Sequence Description of Artificial Sequence Primer 397cagcgttttg 10 398 10 DNA Artificial Sequence Description of Artificial Sequence Primer 398tcgatacagg 10 399 10 DNA Artificial Sequence Description of Artificial Sequence Primer 399gatttaccgc 10 400 10 DNA Artificial Sequence Description of Artificial Sequence Primer 400ggaagtaagc 10 401 10 DNA Artificial Sequence Description of Artificial Sequence Primer 401ttcgttctgc 10 402 10 DNA Artificial Sequence Description of Artificial Sequence Primer 402caacacgatg 10 403 10 DNA Artificial Sequence Description of Artificial Sequence Primer 403caaacggatg 10 404 10 DNA Artificial Sequence Description of Artificial Sequence Primer 404ttacgctgtg 10 405 10 DNA Artificial Sequence Description of Artificial Sequence Primer 405tgctcatacg 10 406 10 DNA Artificial Sequence Description of Artificial Sequence Primer 406gcgtatgttg 10 407 10 DNA Artificial Sequence Description of Artificial Sequence Primer 407gatcaatcgc 10 408 10 DNA Artificial Sequence Description of Artificial Sequence Primer 408acgggtaatg 10 409 10 DNA Artificial Sequence Description of Artificial Sequence Primer 409aaagtccgtg 10 410 10 DNA Artificial Sequence Description of Artificial Sequence Primer 410tgttatgccg 10 411 10 DNA Artificial Sequence Description of Artificial Sequence Primer 411acggatgtag 10 412 10 DNA Artificial Sequence Description of Artificial Sequence Primer 412aaacgctctg 10 413 10 DNA Artificial Sequence Description of Artificial Sequence Primer 413ccatcgtttc 10 414 10 DNA Artificial Sequence Description of Artificial Sequence Primer 414aaatgacgcc 10 415 10 DNA Artificial Sequence Description of Artificial Sequence Primer 415atcgccatac 10 416 10 DNA Artificial Sequence Description of Artificial Sequence Primer 416taaaacgccc 10 417 10 DNA Artificial Sequence Description of Artificial Sequence Primer 417gacattcgtg 10 418 10 DNA Artificial Sequence Description of Artificial Sequence Primer 418gctcataacg 10 419 10 DNA Artificial Sequence Description of Artificial Sequence Primer 419caacatacgc 10 420 10 DNA Artificial Sequence Description of Artificial Sequence Primer 420gatcatagcg 10 421 10 DNA Artificial Sequence Description of Artificial Sequence Primer 421gatcgcattg 10 422 10 DNA Artificial Sequence Description of Artificial Sequence Primer 422accaaacgac 10 423 10 DNA Artificial Sequence Description of Artificial Sequence Primer 423tacctaagcg 10 424 10 DNA Artificial Sequence Description of Artificial Sequence Primer 424tgttatcccg 10 425 10 DNA Artificial Sequence Description of Artificial Sequence Primer 425gttttcgcag 10 426 10 DNA Artificial Sequence Description of Artificial Sequence Primer 426attcgcagtg 10 427 10 DNA Artificial Sequence Description of Artificial Sequence Primer 427gaacggatac 10 428 10 DNA Artificial Sequence Description of Artificial Sequence Primer 428accgtgattc 10 429 10 DNA Artificial Sequence Description of Artificial Sequence Primer 429gcggtaaatc 10 430 10 DNA Artificial Sequence Description of Artificial Sequence Primer 430ctgtcgtttc 10 431 10 DNA Artificial Sequence Description of Artificial Sequence Primer 431ccgactattc 10 432 10 DNA Artificial Sequence Description of Artificial Sequence Primer 432gatctaaccg 10 433 10 DNA Artificial Sequence Description of Artificial Sequence Primer 433aatacacggg 10 434 10 DNA Artificial Sequence Description of Artificial Sequence Primer 434catccgtttg 10 435 10 DNA Artificial Sequence Description of Artificial Sequence Primer 435cacgaatgtc 10 436 10 DNA Artificial Sequence Description of Artificial Sequence Primer 436accgttgttc 10 437 10 DNA Artificial Sequence Description of Artificial Sequence Primer 437tgcgacaatc 10 438 10 DNA Artificial Sequence Description of Artificial Sequence Primer 438tcggtcatag 10 439 10 DNA Artificial Sequence Description of Artificial Sequence Primer 439agcgttcatc 10 440 10 DNA Artificial Sequence Description of Artificial Sequence Primer 440agagcgatac 10 441 10 DNA Artificial Sequence Description of Artificial Sequence Primer 441gtaacgcaac 10 442 10 DNA Artificial Sequence Description of Artificial Sequence Primer 442ataaccgcac 10 443 10 DNA Artificial Sequence Description of Artificial Sequence Primer 443acccgtttac 10 444 10 DNA Artificial Sequence Description of Artificial Sequence Primer 444gatcacgtac 10 445 10 DNA Artificial Sequence Description of Artificial Sequence Primer 445acggtcatac 10 446 10 DNA Artificial Sequence Description of Artificial Sequence Primer 446tattgacgcc 10 447 10 DNA Artificial Sequence Description of Artificial Sequence Primer 447gtcgtcatac 10 448 10 DNA Artificial Sequence Description of Artificial Sequence Primer 448caatagcgac 10 449 10 DNA Artificial Sequence Description of Artificial Sequence Primer 449aatacgccac 10 450 10 DNA Artificial Sequence Description of Artificial Sequence Primer 450gtttacggtg 10 451 10 DNA Artificial Sequence Description of Artificial Sequence Primer 451tctactcgtg 10 452 10 DNA Artificial Sequence Description of Artificial Sequence Primer 452tgaccgtaac 10 453 10 DNA Artificial Sequence Description of Artificial Sequence Primer 453gatttacgcg 10 454 10 DNA Artificial Sequence Description of Artificial Sequence Primer 454gtatccgttc 10 455 10 DNA Artificial Sequence Description of Artificial Sequence Primer 455acatacgagc 10 456 10 DNA Artificial Sequence Description of Artificial Sequence Primer 456caccgtaaac 10 457 10 DNA Artificial Sequence Description of Artificial Sequence Primer 457gttcgtaagc 10 458 10 DNA Artificial Sequence Description of Artificial Sequence Primer 458tccgtatgtc 10 459 10 DNA Artificial Sequence Description of Artificial Sequence Primer 459tgcgacatac 10 460 10 DNA Artificial Sequence Description of Artificial Sequence Primer 460cccgtaaatc 10 461 10 DNA Artificial Sequence Description of Artificial Sequence Primer 461gtcgctattg 10 462 10 DNA Artificial Sequence Description of Artificial Sequence Primer 462tgattagcgg 10 463 10 DNA Artificial Sequence Description of Artificial Sequence Primer 463tgacgatagc 10 464 10 DNA Artificial Sequence Description of Artificial Sequence Primer 464gcttacgaac 10 465 10 DNA Artificial Sequence Description of Artificial Sequence Primer 465gaatagtcgg 10 466 10 DNA Artificial Sequence Description of Artificial Sequence Primer 466gttgcgttac 10 467 10 DNA Artificial Sequence Description of Artificial Sequence Primer 467acagcgtatg 10 468 10 DNA Artificial Sequence Description of Artificial Sequence Primer 468atgcgtaagg 10 469 50 DNA Homo sapiens 469tataaaaagg gcccacaaga gaccggctct aggatcccaa ggcccaactc 50 470 20 DNA Homo sapiens 470aggatcccaa ggcccaactc 20 471 19 DNA Homo sapiens 471ggatcccaag gcccaactc 19 472 12 DNA Homo sapiens 472aaggcccaac tc 12

Claims

1. A method for synthesizing cDNA including a 5-terminal sequence of a full-length mRNA with a cap structure from a mRNA sample containing the full-length mRNA with the cap structure and a non-full-length mRNA without a cap structure in a mixture, comprising:(a) removing the phosphate group at the 5′-terminus of the non-full-length mRNA in the mRNA sample; (b) removing the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample; (c) ligating an oligoribonucleotide of a predetermined sequence to the phosphate group at the 5′-terminus of the mRNA generated by step (b) in the sample, said oligoribonucleotide having a sequence prepared by generating a number of oligonucleotide sequences including various combinations of bases in a predetermined number, carrying out a homology search with a predetermined nucleotide sequence data base to determine the occurrence number of a sequence completely matching or differing by one base, and preparing a combination of plural sequences in a low-frequency occurrence group including a sequence at the lowest occurrence number; and (d) subjecting the mRNA ligated with the oligoribonucleotide at the phosphate group at the 5′-terminus to a reverse transcriptase process using as a primer a short-chain oligonucleotide capable of being annealed to an intermediate sequence within the mRNA, to synthesize a first-strand cDNA, wherein said oligoribonucleotide has a sequence selected from the group consisting of: 5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAAGG-3′ (SEQ ID NO;1), 5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:2), 5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:3), 5′-AAGGUACGCC-GUUGCGUUAC-ACAGCCUAUG-AUGCGU-3′ (SEQ ID NO:4), 5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:5), 5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:6) and 5′-CUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO: 7).

2. The method according to claim 1, wherein the step (c) comprises ligating an oligoribonucleotide comprising a sequence not contained in the sequence of the mRNA in the mRNA sample, to the phosphate group.

3. The method according to claim 1, wherein the primer used in step (d) comprises a short-chain oligonucleotide of a length of 6 bases or longer.

4. The method according to claim 1, wherein step (b) comprises removing the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample by contacting the full-length mRNA with a tobacco acid pyrophosphatase purified to a high purity with no contamination of trace amounts of nuclease cleaving the phosphodiester bond comprising RNA and a phosphatase removing 5′-phosphate group freshly generated after cap cleavage.

5. A method for synthesizing cDNA including the 5′-terminal sequence of full-length mRNA with a cap structure from a mRNA sample containing a full-length mRNA with the cap structure and a non-full-length mRNA without a cap structure in a mixture, comprising:(a) removing the phosphate group at the 5′-terminus of the non-full-length mRNA in the mRNA sample; (b) removing the cap structure at the 5′-terminus of the full-length mRNA in the mRNA sample by contacting the full-length mRNA with a tobacco acid pyrophosphatase purified to a high purity with no contamination of trace amounts of nuclease cleaving the phosphodiester bond comprising RNA and a phosphatase removing 5′-phosphate group freshly generated after cap cleavage; (c) ligating an oligoribonucleotide of a predetermined sequence to the phosphate group at the 5′-terminus of mRNA generated by step (b) in the sample, said oligoribonucleotide comprising a sequence prepared by using a combination of plural oligonucleotide sequences in a low occurrence frequency group including an oligonucleotide sequence with the lowest occurrence number among sequences completely matching with or differing by one base from plural 10-mer oligonucleotide sequences of various different base combinations in a predetermined nucleotide data base; (d) subjecting the mRNA ligated with the oligoribonucleotide at the phosphate group at the 5′-terminus to a reverse transcriptase process using as a primer a short-chain oligonucleotide capable of being annealed to an intermediate sequence within the mRNA, to synthesize a tirst-strand cDNA; and (e) synthesizing a second-strand cDNA based on the resulting first-strand cDNA, wherein said oligoribonucleotide has a sequence selected from the group consisting of: 5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAAGG-3′ (SEQ ID NO:1), 5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:2), 5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:3), 5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:4), 5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:5), 5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:6) and 5′-GUUGCGUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:7).

6. The method according to claim 5, wherein the tobacco acid pyrophosphatase removes the cap structure at the 5′-terminus and is purified at an extent such that the tobacco acid pyrophosphatase substantially never contains other enzymes cleaving the remaining sites within mRNA.

7. The method according to claim 5, wherein the oligonucleotide has a sequence designed by using a combination of plural oligonucleotide sequences in the low occurrence frequency group including an oligonucleotide sequence with the lowest occurrence frequency, among sequences completely matching with or differing by one base from the plural 10-mer oligonucleotide sequences of various different base combinations in a predetermined nucleotide sequence data base.

8. The method according to claim 7, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAAGG-3′ (SEQ ID NO:1).

9. The method according to claim 7, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:2).

10. The method according to claim 7, wherein sad oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:3).

11. The method according to claim 7, wherein said oligoribonucleotide has the sequence of:5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′(SEQ ID NO:4).

12. The method according to claim 7, wherein said oligoribonucleotide has the sequence of:5′-AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:5).

13. The method according to claim 6, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:6).

14. The method according to claim 7, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:7).

15. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAAGG-3′ (SEQ ID NO:1).

16. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:2).

17. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′ -GUUCGCGUUAC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:3).

18. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′ -AAGGUACGCC-GUUGCGUUAC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:4).

19. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′-AAGGUACGCC-GWGCGUUAC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:5).

20. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGU-3′ (SEQ ID NO:6).

21. The method according to claim 1, wherein said oligoribonucleotide has the sequence of:5′-GUUGCGUUAC-AAGGUACGCC-ACAGCGUAUG-AUGCGUAA-3′ (SEQ ID NO:7).