Analysis of predisposition based on human airway trypsin protease gene polymorphism

TECHNICAL FIELD

This invention relates to a method for predicting the constitution susceptible to the onset of specific diseases, effects on methods of treatment for patients suffering from said diseases or predicting the prognosis of the treatment by analysis of genetic polymorphisms of a human trypsin-like enzyme of a respiratory tract.

BACKGROUND ART

Research on related genes has recently been promoted not only in genetic diseases due to deletion or mutation of single genes but also in multifactorial diseases caused by entanglement of several genetic predispositions and environmental factors. As a result, the deletion or point mutation and isoforms related to the multifactorial diseases and further mutation of genetic parts (introns or promoters) without affecting actually translated amino acid sequences have come to be considered as risk factors for the diseases.

EFFECT OF THE INVENTION

It has been published that the correlation is recognized between bone density and genetic polymorphisms of an intron of the vitamin D receptor in the osteopathic field as the prior art (Morrison, N. A. et al., Nature, 367: 284-287 1994). In the field of circulatory organs, it has been reported that the I type (insertion type) and D type (deletion type) genetic polymorphisms of an angiotensin-converting enzyme are associated with the onset of myocardial infarctions (Cambien, F. et al., Nature 359: 641-644, 1992) and the amino acid substitution of M295T of angiotensinogen and the polymorphisms of a promoter region of G-6A are associated with the onset of essential hypertension (Inoue, I. et al., J. Clin. Invest., 99: 1786-1797, 1997). Furthermore, in the field of the nervous system, it has been reported on the association between the onset of dementia and the isoforms of apoE protein. Much research has been carried out in the association between the genetic polymorphisms of glutathione S-transferase and the onset of cancers in the cancer-related field. As the field of respiratory diseases, it has been reported on the association between the onset or morbid state of asthma and the TNF (Moffatt, M. F. et al., Hum. Mol. Genet. 6 (4): 551-554, 1997) and the association between the onset or morbid state of the asthma and the genetic polymorphisms of an angiotensin converting enzyme (Benessiano, J. et al., J. Allergy Clin. Immunol. 99 (1): 53-57, 1997).

Furthermore, attention has been paid to the genetic background as one of causes of difference between patients in sensitivity to drugs used for treating diseases, and it is has been desired even by the medical site to provide the directionality such as selection of methods of treatment according to the drug sensitivity of individual humans by diagnosis of the genetic polymorphisms. It is thought that the drug development by selecting patient groups expectable of drug effects according to the genetic polymorphisms is effective in clinical trials (Kleyn K. W. et al., Science, 281: 1820-1821, 1998). A report on the genetic polymorphisms of an intron of an angiotensin converting enzyme [ACE (angiotensin converting enzyme)] and effects of an ACE inhibitor (Yoshida, H. et al., J. Clin. Invest. 96: 2162-2169, 1995), a report on the genetic polymorphisms of beta 2-adrenergic receptor and effects of the beta-agonist on asthma (Liggett, S. B., Am. J. Respir. Crit. Care Med. 156 (4 Pt 2): S156-162, 1997) and the like are cited as the conventional reports related to the drug sensitivity and the genetic polymorphisms.

On the other hand, the human trypsin-like enzyme of the respiratory tract related to the present invention has been purified from the sputum of patients suffering from chronic airway diseases (Japanese Unexamined Patent Publication No. 7-067640 and Yasuoka, S. et al., Am. J. Respir.Cell Mol. Biol., 16: 300-308, 1997) and the amino acid sequence and cDNA sequence thereof have been already made clear (Japanese Unexamined Patent Publication No. 8-89246 and Yamaoka K. et. al., J. Biol. Chem., 273(19): 11895-11901, 1998). Several studies have been made of the activity possessed by the enzyme in vitro. Since the enzyme has production enhancing actions on cytokines such as IL-8 or GM-CSF derived from a human bronchial epithelial cell line including the association with mucociliary movement, the possibility for association with the morbid state of airway inflammations is considered (Terao, Noriko et al., the Japanese Respiratory Society, 1998). Since the enzyme has enzyme activities such as hydrolytic activity for fibrinogen and activating actions on plasminogen activators (pro-urokinase) (Yoshinaga, Junko et al., Conference on Proteases and Inhibitors in Pathophysiology and Therapeutics, 1998), the possibility is assumed for anti-inflammatory actions through the formation of fibrins on the airway mucosal surfaces or modification of the morbid state thereof in chronic airway diseases and the possibility is also considered for the association with cancer metastasis or the like. The association of the enzyme with physiological functions or the morbid state in vivo is not yet sufficiently elucidated, and the genetic parts (introns or promoters) without corresponding to the actually translated amino acid sequences has not yet known about genes at all. Further, no investigation has hitherto been carried out on the association of the presence or absence of the genetic polymorphisms for the human trypsin-like enzyme of the respiratory tract or the genetic polymorphisms with diseases.

By the way, much information can be provided about the prediction of the onset of specific diseases, prognosis of treatment, selection of appropriate methods of the treatment and administered drugs or the like by the prediction of diseases-associated constitution by genetic analysis. Accordingly, the prediction is desired by many physicians and patients and further makes the prophylaxis of onset and early therapy possible. Therefore, it is thought that the prediction is related with a reduction in medical care expenditures to become indispensable for the future medical care.

It is, however, very difficult to find out a gene associated with diseases and establish an analytical method therefor, and there are few examples of genetic analytical methods in which the association with diseases is recognized as described above. Therefore, the development of the genetic analytical technique for making various disease-associated constitutions predictable is strongly desired.

On the other hand, it is not yet elucidated with what diseases the human trypsin-like enzyme of the respiratory tract is associated at present.

DISCLOSURE OF THE INVENTION

As a result of intensive research made in consideration of the problems of the prior art, the present inventors et al. have designed a primer for genetically amplifying an intron part on the genome of the human trypsin-like enzyme of the respiratory tract specifically expressing in the human respiratory tract, novelly determined the DNA sequence of both the termini of the amplified genetic fragment and the novelly determined DNA sequence in an exonlintron border part, found out that there are genetic polymorphisms in the amplified genetic fragment and the novelly determined DNA sequence and further firstly found out the association of the genotypes of the human trypsin-like enzyme of the respiratory tract with diseases in individual humans by analyzing the genetic polymorphisms, thus attaining the present invention.

That is, an object of the present invention is to provide a method for predicting the constitution of individual humans susceptible to the onset of specific diseases or effects of treatment on patients or prognosis of the treatment by analyzing the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract.

Further, the present invention is a method for diagnosing an abnormality in the mucociliary biophylactic system by the analysis of the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract and a method for predicting the constitution of individual humans susceptible to the onset of diseases, effects of treatment on patients or prognosis of the treatment.

Furthermore, the present invention is a genetic fragment containing a part or all of the base sequence of an intron in the human trypsin-like enzyme of the respiratory tract.

BRIEF DESCRIPTION OF DRAWINGS

FIG. 1

illustrates agarose gel electrophoretic patterns of DNA fragments containing an intron region of a gene encoding a mature protein of the human trypsin-like enzyme of the respiratory tract obtained by genetic amplification. It is observed that lanes 1 and 5 are markers (10 Kb, 7 Kb, 5 Kb, 4 Kb, 3 Kb, 2.5 Kb, 2 Kb, 1.5 Kb and 1 Kb from above), lane 2 is a DNA fragment of about 6 Kb amplified by primers A1 (SEQ ID NO: 7) and A2 (SEQ ID NO: 8), lane 3 is a DNA fragment of about 1.5 Kb amplified by primers B1 (SEQ ID NO: 9) and B2 (SEQ ID NO: 10) and lane 4 is a DNA fragment of about 3.4 Kb amplified by primers C1 (SEQ ID NO: 11) and C2 (SEQ ID NO: 12).

FIG. 2

illustrates agarose gel electrophoretic patterns of DNA fragments containing an intron region of a gene encoding a propeptide of the human trypsin-like enzyme of the respiratory tract obtained by genetic amplification. It is observed that lanes 1 and 4 are markers (10 Kb, 7 Kb, 5 Kb, 4 Kb, 3 Kb, 2.5 Kb, 2 Kb, 1.5 Kb and 1 Kb from above), lane 2 is a DNA fragment of about 5.5 Kb amplified by primers D1 (SEQ ID NO: 13) and D2 (SEQ ID NO: 14) and lane 3 is a DNA fragment of about 5 Kb amplified by primers E1 (SEQ ID NO: 15) and E2 (SEQ ID NO: 16).

FIG. 3

illustrates relative positions of introns A, B and C on the human trypsin-like enzyme genome of the respiratory tract and agarose gel electrophoretic patterns of genetic polymorphisms (RFLP) of the intron A detected by TaqI and of the intron C detected by MboI and BstUI.

FIG. 4

illustrates the nucleic acid sequence of intron C (SEQ ID NO: 17), designates the location of 5′ and 3′ boundaries of the intron, and indicates the specification restriction endonuclease recognition sites in intron C.

BEST MODE FOR CARRYING OUT THE INVENTION

According to the present invention, there are provided a method for predicting the association of the constitution of individual humans with specific diseases and a genetic fragment or a DNA sequence used for the genetic analysis thereof.

Respiratory diseases, pulmonary cancer, especially pulmonary emphysema (PE), sinobronchial syndrome, diffuse panbronchiolitis (DPB) and bronchiectasis (BE) belonging to chronic obstructive pulmonary diseases (COPD) or abnormalities in the mucociliary biophylactic system are exemplified as specific diseases for judging the constitution susceptible to the onset or specified diseases for predicting the judgment on effects of treatment thereof or prognosis of the treatment by the method of the present invention.

Analysis of the genotypes classified by detecting one or more base mutations and analysis of the haplotypes classified by detecting one or more of the base mutations are exemplified as an analytical method for the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract in the present invention.

The analytical method for the genetic polymorphisms of the trypsin-like enzyme of the respiratory tract is carried out by, for example, an analytical method by a restriction fragment length polymorphisms (RFLP) according to the cleavage with a restriction enzyme. The analytical method for the genetic polymorphisms in the present invention includes even an analytical method for the genetic polymorphisms detectable by the Southern hybridization using a cDNA sequence of the human trypsin-like enzyme of the respiratory tract. That is, it is a method for cleaving the genomic DNA with a restriction enzyme capable of detecting the genetic polymorphisms disclosed in the present invention, then carrying out a gel electrophoresis, performing transcription to a nitrocellulose membrane or the like and subsequently analyzing the cleaved patterns of the human trypsin-like enzyme genome of the respiratory tract using the human trypsin-like enzyme cDNA of the respiratory tract as a probe. The analysis can be made even by a method for amplifying a DNA fragment by PCR so as to include sites for the genetic polymorphisms, then converting the amplified DNA fragment into a single strand and analyzing the resulting single strand by a difference in mobility of electrophoresis [PCR-single strand conformation polymorphism (SSCP)] method or the like. Furthermore, many methods such as a mismatch PCR method, a PCR-allele specific oligo (ASO) method using an allele specific oligonucleotide, a method for judgment by carrying out annealing using an oligo probe or a pinpoint sequencing method for directly determining the base sequence of the genetic polymorphic sites are cited as the method for making the detection of the polymorphic sites possible, and the analytical method for the genetic polymorphisms can be applied even to genetic diagnosis by using a DNA chip.

An intron may be used as sites for analysis of the genetic polymorphisms, and the following genetic fragments are exemplified as the site for analysis of the specific genetic polymorphisms:

(a) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 7 and SEQ ID NO: 8,

(b) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 9 and SEQ ID NO: 10,

(c) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 11 and SEQ ID NO: 12,

(d) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 13 and SEQ ID NO: 14,

(e) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 15 and SEQ ID NO: 16,

(f) a genetic fragment containing intron C amplifiable by using the primers represented by SEQ ID NO: 11 and SEQ ID NO: 12, and

(g) a genetic fragment containing intron A amplifiable by using the primers represented by SEQ ID NO: 7 and SEQ ID NO: 8.

In the intron C, a genetic fragment containing a sequential part recognized herein by a restriction enzyme BstUI, MboI, MseI or FbaI is exemplified as the sites for analysis of the genetic polymorphisms. In the intron A, a part containing a sequential part recognized by a restriction enzyme MboI, TaqI or AfaI, one of the genetic polymorphic sites represented by SEQ ID NO: 17 or a combination of one or more thereof is exemplified as the sites for the analysis of the genetic polymorphisms. The genotypic or haplotypic classification is judged by the analysis of the sites.

Furthermore, the present invention is a genetic fragment containing a part or all of the base sequence of an intron in the human trypsin-like enzyme of the respiratory tract and the following genetic fragments are especially exemplified:

(a) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 7 and SEQ ID NO: 8,

(b) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 9 and SEQ ID NO: 10,

(c) a genetic fragment containing an intron region ampliflable by using the primers represented by SEQ ID NO: 11 and SEQ ID NO: 12,

(d) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 13 and SEQ ID NO: 14,

(e) a genetic fragment containing an intron region amplifiable by using the primers represented by SEQ ID NO: 15 and SEQ ID NO: 16,

(f) a genetic fragment containing an intron in the human trypsin-like enzyme of the respiratory tract comprising the base sequence represented by any of SEQ ID NOS: 1-6 or a genetic fragment sandwiched between the base sequences, and

(g) a genetic fragment of the intron C in the human trypsin-like enzyme of the respiratory tract comprising the base sequence represented by SEQ ID NO: 17.

EXAMPLES

The present invention is explained in detail hereinafter by way of examples, provided that the examples are not intended as a definition of the method for predicting the disease-associated constitution by the analysis of the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract.

Standard Methods for Operations

Standard DNA extracting operations, genetic amplifying operations, restriction enzyme cleavage operations and electrophoretic operations usable in the present invention are explained hereinafter.

(a) Standard DNA Extracting Operations

Nothing is especially limited in biosamples used for the genetic amplification of the present invention; however, blood corpuscle components are suitable because specimens are readily collected and DNA is easily extracted.

1. The whole blood in a volume of 0.5 ml (using a 2Na-EDTA anticoagulant) is placed in a micro-centrifugal tube having a capacity of 1.5 ml.

2. A dissolvent in a volume of 0.5 ml is added to the tube, and the tube is lightly tapped several times. The tube is then turned upside down, and the liquids are mixed.

(The following mixing operations are performed according to the above procedures).

An example of the dissolvent: 1×SSC

This is prepared by diluting 20×SSC regulated to pH 7.0 with 10N NaOH containing 175.3 grams of NaCl and 88.2 grams of sodium citrate in 1 liter 10-fold.

3. The mixture is centrifuged (at 4° C. and 10,000 g for 20 seconds), and the supernatant is then removed so as not to discharge dark pellets.

4. The dissolvent in a volume of 1 ml is added to stir the mixture

5. The mixture is centrifuged (at 4° C. and 10,000 g for 20 seconds), and the supernatant is then removed.

6. Steps 4 and 5 are repeated once more.

7. An enzyme reaction solution in a volume of 200 μl and a proteolytic enzyme in a volume of 10 μl are added and mixed therewith. An example of the enzyme reaction solution: A mixture liquid of 0.04 M DTT (dithiothreitol) with 0.2 M NaOAc (sodium acetate) and 0.4%SDS

An example of the proteolytic enzyme liquid:

A 10 mg/ml proteinase (Proteinase K)

8. The mixture is kept warm at 37° C. for 1 hour (the mixture is mixed by lightly shaking 2 to 3 times in the course thereof).

9. A solution of sodium iodide in a volume of 300 μl is added and mixed therewith.

10. Isopropyl alcohol in a volume of 0.5 ml is added and mixed until a white linear DNA is completely visible.

11. The resulting mixture is centrifuged (at room temperature and 10,000 g for 10 minutes), and the supernatant is then slowly removed. The solution remaining in a tube wall is sufficiently removed by a method for placing the tube on a filter paper upside down or the like.

12. A wash liquid (A) in a volume of 1 ml is added and mixed therewith. The mixture is sufficiently mixed so as to peel a precipitate from the tube wall.

An example of the wash liquid (A): 70% EtOH

13. The resulting mixture is centrifuged (at room temperature and 10,000 g for 5 minutes), and the supernatant is then removed.

14. A wash liquid (B) in a volume of 1 ml is added, and the prepared mixture is sufficiently mixed so as to peel the precipitate from the tube wall.

An example of the wash liquid (B): 80% EtOH

15. The mixture is centrifuged (at room temperature and 10,000 g for 5 minutes), and the supernatant is then removed.

16. The DNA precipitate is lightly vacuum-dried (the drying time is within 3 minutes because the DNA is sparingly dissolved when drying the precipitate too much).

(a) Standard Genetic Amplifying Operations

Although several principles are known about the genetic amplifying method, the polymerase chain reaction method (PCR method) is described as a standard one hereinafter.

Composition of the reaction solution: 50 mM of KCl, 10 mM of Tris-HCl (pH 9.0, 25° C.), 0.1% of TritonX-100, 1.5 mM of MgCl

2

, 2 mM of dNTPs, 15 μM of Forward Primer, 15 μM of Reverse Primer, 1 mg/l of a genomic DNA and 1 unit of TaqDNA polymerase, the total volume of 50 μl

Reaction cycle: at 94° C. for 1 minute, 64° C. for 1 minute and 72° C. for 1 minute as one cycle. The reaction is conducted for 40 cycles.

Primers used are the following C1 (35 bases) and C2 (35 bases):

C1: 5′-GGAGC CATCT TGTCT GGAAT GCTGT GTGCT GGAGT-3′ (SEQ ID NO: 11)

C2: 5′-CACAA TAAAC CAAAG CCGCC GTGAG TCTTC TTGTA-3′ (SEQ ID NO: 12)

(c) Standard Restriction Enzyme Cleavage Operations

Composition of the reaction solution for MboI: 10 mM of Tris-HCl (pH7.4), 10 mM of MgCl

2

, 100 mM of NaCl, 10 mM of KCl, 1 mM of DTT and 100 μg/ml of BSA (bovine serum albumin)

MboI at a concentration of 10 units/20 μl of reaction solution is added to carry out incubation at 37° C. for 3 hours.

(b) Standard Electrophoretic Operations

The buffer solution for electrophoresis is 0.5×TBE, with the proviso that 5×TBE contains 54 grams of Tris base, 27.5 grams of boric acid and 1 mM of EDTA in 1 liter and is regulated to pH 8.0. The above buffer solution is used to carry out electrophoresis under a voltage of 100 V for 30 minutes by using a 1% or a 3% agarose gel [using Seakem GTA Agarose (FMC Bio Products)] (containing 0.5 μl/ml of ethydium bromide). The band of the DNA is then observed with a UV lamp.

Example 1

Obtaining of DNA Fragment Containing an Intron on Human Trypsin-like Enzyme Genome of the Respiratory Tract and Analysis of Base Sequence Thereof

In order to search for an intron site on the genome of a mature human trypsin-like enzyme of the respiratory tract, primers were prepared by referring to the constitution of exons and introns of the genome of several typtase analogous enzymes to amplify a human genomic DNA. A DNA fragment (genetic fragment) of about 6 KB was amplified by the primers A1 (SEQ ID NO: 7) and A2 (SEQ ID NO: 8), and a DNA fragment of about 1.5 Kb was amplified by the primers B1 (SEQ ID NO: 9) and B2 (SEQ ID NO: 10). A DNA fragment of about 3.4 Kb was amplified by the primers C1 (SEQ ID NO: 11) and C2 (SEQ ID NO: 12). (

FIG. 1

)

The DNA fragments were excised from gels and purified, and the respective fragments were inserted into TA cloning vectors (manufactured by Invitrogen Corporation). The base sequences on both sides (5′-terminus and 3′-terminus) of the insert DNA were determined for several clones thereof to find that the cDNA sequence of the human trypsin-like enzyme of the respiratory tract was present contiguous to the sequences of the primers, consensus sequences were recognized as contiguous thereto in border regions of the exon-intron on both sides of the 5′-terminus and the 3′-terminus and the amplified DNA fragment was a DNA fragment containing the intron region in the human trypsin-like enzyme of the respiratory tract.

The sequences of the introns which have been made clear in the present invention in a genetic region encoding the mature protein of the human trypsin-like enzyme of the respiratory tract are respectively referred to as intron A, intron B and intron C from the 5′-side. (FIG.

3

). The base sequences at the 5′- and 3′-termini of the clarified respective introns are as represented by SEQ ID NOS: 1, 2, 3, 4, 5 and 6. As for the intron C, the whole base sequence is represented by SEQ ID NO: 17.

On the other hand, several primers were prepared for the region encoding a propeptide of the human trypsin-like enzyme of the respiratory tract to carry out the genetic amplification. Thereby, it was clear that a DNA fragment of about 5.5 Kb was amplified by the primers D1 (SEQ ID NO: 13) and D2 (SEQ ID NO: 14) and a DNA fragment of about 5 Kb was amplified by the primers E1 (SEQ ID NO: 15) and E2 (SEQ ID NO: 16). (FIG.

2

). The genetic fragments are regarded as containing the introns.

Example 2

Analysis of Genetic Polymorphisms of Introns in Human Trypsin-like Enzyme of the Respiratory Tract

In order to investigate whether or not the genetic polymorphisms are present in the introns A, B and C, the genomic DNA of normal 23 humans was extracted from the whole blood (the standard method for operations) and respectively amplified by the primers A1 and A2 for amplifying the intron A, the primers B1 and B2 for amplifying the intron B and the primers C1 and C2 for amplifying the intron C according to the PCR to compare the cleavage patterns with various kinds of restriction enzymes. As a result, it was found that the genetic polymorphisms were observed with the restriction enzymes MboI, TaqI and AfaI in the intron A.

Conversely, the genetic polymorphisms were not observed by restriction enzymes Tsp509I, AluI, NlaIII, MspI, BstUI, BfaI, HinPI, HaeIII, HindIII, SspI, PstI, EcoRI, SalI and EcoRV.

In the intron B, the genetic polymorphisms were not observed by the restriction enzymes Tsp509I, AluI, NlaIII, MspI, BstUI, BfaI, HinPI, HaeIII, MboI, AfaI, TaqI, MseI, ClaI, NsiI, EcoT14I, NdeI, PmlI, ApaLI, AatII, ApaI, KpnI, BsmI, HindIII, SspI and EcoRV.

In the intron C, it was found that the genetic polymorphisms were observed by the restriction enzymes MboI, BstUI, MseI and FbaI. Conversely, the genetic polymorphisms were not observed by restriction enzymes AluI, NlaIII, MspI, BfaI, HinPI, HaeIII, AfaI, TaqI, HindIII, SspI, BglII, EcoT14I, PvuII, PvuI, EcoRI, BamHI, EcoRV and KpnI.

When the DNA fragment containing the intron C amplified by using a combination of the primers C1 and C2 was cleaved with the MboI or BstUI, experiments on cleavage by the MboI revealed that the case where a band appeared at 1.3 Kb could be judged as genotype MM, the case where a band appeared at 1.05 Kb could be judged as genotype mm and the case where two bands appeared together at 1.3 Kb and 1.05 Kb could be judged as genotype Mm according to the electrophoresis. On the other hand, in the case of the BstUI, the case where a band appeared at 3.4 Kb could be judged as BB, the case where two bands appeared at 2.45 Kb and 0.95 Kb could be judged as bb and the case where three bands appeared together could be judged as Bb.

FIG. 3

shows electrophoretic patterns of the genetic polymorphisms of the intron A detected by TaqI, and of the intron C detected by MboI and BstUI. Furthermore, the whole base sequence of the bm type haplotype was determined for the intron C from the DNA fragment obtained from the genome of one example of a bbmm type normal human by PCR (SEQ ID NO: 17) The genetic polymorphic sites detected by BstUI and MboI in the base sequence of the intron C are indicated by arrows with white spaces.

The base sequence of one example of a patient suffering from the BBmm type BE was determined to find that the base sequence of the Bm haplotype BstUI genetic polymorphic sites were not cleaved with the BstUI because CGCG was converted into ACCG.

Example 3

Analysis of Disease-associated Constitution by the Analysis of the Intron Genetic Polymorphisms of Human Trypsin-like Enzyme of the Respiratory Tract

As for the statistical analysis, the analysis was made according to the chi-square test using a statistical analysis software Stat View4.02 (Abacus Concepts Co.).

Example 3-1

Analysis of Disease-associated Constitution by Genotypic Classification

Among the genotypes disclosed in Example 2, investigation was made whether or not the classification of diseases associated with the human trypsin-like enzyme of the respiratory tract can be made for the genetic polymorphisms detected with the MboI and BstUI in the intron C. The diseases selected as objects are diffuse panbronchiolitis (DPB), bronchiecstasis (BE), pulmonary emphysema (PE) and bronchial asthma (BA) which are respiratory diseases.

The genotypes of each human were judged by selecting 106 normal humans, 29 patients suffering from the diffuse panbronchiolitis (DPB), 38 patients suffering from the bronchiecstasis (BE), 22 patients suffering from pulmonary emphysema (PE) and 32 patients suffering from the bronchial asthma (BA) according to the standard method for operations. MboI and BstUI were used as the restriction enzymes.

The number of humans having the occurrence and the frequency of occurrence of each genotype and the number of occurrence and the frequency of occurrence of each allelic type were as shown in Tables 1 and 2.

TABLE 1

BstUI genotype

Number of humans having

Number of

the occurrence (humans)

occurrence (allele)

BB

Bb

bb

Total

B

b

Total

Normal

16

55

35

106

Normal

87

125

212

DPB

8

12

9

29

DPB

28

30

58

BE

11

15

12

38

BE

37

39

76

PE

5

12

5

22

PE

22

22

44

BA

2

12

18

32

BA

16

48

64

Frequency of

Frequency of occurrence (%)

occurrence (%)

BB

Bb

bb

B

b

Normal

15.1

51.9

33.0

Normal

41.0

59.0

DPB

27.6

41.4

31.0

DPB

48.3

51.7

BE

28.9

39.5

31.6

BE

48.7

51.3

PE

22.7

54.5

22.7

PE

50.0

50.0

BA

6.3

37.5

56.3

BA

25.0

75.0

TABLE 2

MboI genotype

Number of humans having

Number of

the occurrence (humans)

occurrence (allele)

MM

Mm

mm

Total

M

m

Total

Normal

10

40

56

106

Normal

60

152

212

DPB

3

7

19

29

DPB

13

45

58

BE

3

15

20

38

BE

21

55

76

PE

3

6

13

22

PE

12

32

44

BA

1

12

19

32

BA

14

50

64

Frequency of

Frequency of occurrence (%)

occurrence (%)

MM

Mm

mm

M

m

Normal

9.4

37.7

52.8

Normal

28.3

71.7

DPB

10.3

24.1

65.5

DPB

22.4

77.6

BE

7.9

39.5

52.6

BE

27.6

72.4

PE

13.6

27.3

59.1

PE

27.3

72.7

BA

3.1

37.5

59.4

BA

21.9

78.1

Tables 1 and 2 show that the frequency of occurrence of BB type manifests a higher tendency in the DPB, BE and PE by judging the above genotypes. That is, the judgment can be made that individual humans having the genotypes have constitutions susceptible to the DPB, BE and PE. Furthermore, when the DPB, BE and PE are collected into the patient groups suffering from the respiratory three diseases according to the classification of the chronic obstructive pulmonary diseases (COPD), results are obtained as follows: The frequency of occurrence of the BB type is statistically significantly higher than that of normal humans (chi-square p value=0.04 and chi-square value=4.2).

BB

NotBB

Total

Frequency of observation

Three diseases, BB/NotBB

Normal

16

90

106

Respiratory

24

65

89

3 diseases

Total

40

155

195

Percent (row):

Three diseases, BB/Not BB

Normal

15

85

100

Respiratory

27

73

100

3 diseases

Total

21

79

100

Example 3-2

Analysis of Disease-related Constitution by Haplotypic Classification

Frequency of Occurrence of Haplotypes

The number of humans having the occurrence and the frequency of occurrence of the haplotypes according to a combination of both genetic polymorphisms of BstUI and MboI in 106 normal humans, 29 patients suffering from diffuse panbronchiolitis (DPB), 38 patients suffering from bronchiectasis (BE), 22 patients suffering from pulmonary emphysema (PE) and 32 patients suffering from bronchial asthma (BA) are shown in the tables. As a result of investigation on 238 humans, the tables suggest that the bM haplotype is almost absent in Japanese due to the absence of anyone having the genotypes of Bb-MM, bb-MM and bb-Mm at all.

Number of humans having the occurrence (humans)

BB-

BB-

BB-

Bb-

Bb-

Bb-

bb-

bb-

bb-

MM

Mm

mm

MM

Mm

mm

MM

Mm

mm

Total

Normal

10

6

0

0

34

21

0

0

35

106

DPB

3

2

3

0

5

7

0

0

9

29

BE

3

7

1

0

8

7

0

0

12

38

PE

3

0

2

0

6

6

0

0

5

22

BA

1

1

0

0

11

1

0

0

18

32

As for the following analysis, the statistical technique (chi-square method) was used to promote the analysis of the association with respiratory diseases on the assumption that the human trypsin-like enzyme of the respiratory tract genetic haplotypes of Japanese were the three kinds of BM, Bm and bm (when the number of occurrence was 5 or more, the chi-square p values were used as the following p values and the Fisher's direct method p values were indicated as the following p values in the case of 2×2 table including a frame of the number of occurrence of 4 or below).

Allelic Classification (1)

The investigation was made on the frequency of occurrence of each allele for three kinds of haplotypes of Japanese to find that there was a deviation in distribution of the frequency of occurrence between the respiratory three disease groups (DPB, BE and PE) belonging to the COPD and normal humans with a statistical significant difference (p=0.027). Particularly, the frequency of occurrence of Bm allele was higher in the respiratory three disease groups (DPB, BE and PE) belonging to the COPD than in normal humans.

The frequency of occurrence of Bm allele in the BE, DPB and PE was high with regard to each disease.

Conversely, the frequency of occurrence of Bm allele was lower for the BA.

Frequency of observation:

Three diseases, allele

Bm.

BM

b.m.

Total

Normal

27

60

125

212

Respiratory

41

46

91

178

3 diseases

Total

68

106

216

390

Contingency table analytical statistics:

Three diseases, allele

Number of missing values

107

Degree of freedom

2

Chi-square value

7.174

Chi-square p value

.0277

G-square value

7.164

G-square p value

.0278

Contingency table analytical

.134

coefficient

Cramer's V value

.136

Frequency of observation: BE, allele

Bm.

BM

b.m.

Total

BE

16

21

39

76

Normal

27

60

125

212

Total

43

81

164

288

Contingency table analytical statistics:

PE, allele

Number of missing values

241

Degree of freedom

2

Chi-square value

3.040

Chi-square p value

.2187

G-square value

2.765

G-square p value

.2510

Contingency table analytical

.108

coefficient

Cramer's V value

.109

Allelic Classification (2)

Since the association of the Bm alleles with diseases is considered as strong from the above description, the relation of the number of Bm type alleles with the number of alleles other than the Bm type was analyzed by paying special attention to the type.

In view of the respiratory three disease groups (DPB, BE and PE) belonging to the COPD, the frequency of occurrence of the Bm allele is definitely higher in the patient groups suffering from the respiratory three diseases than that in the normal humans when the patient groups suffering from the three respiratory disease groups are compared with normal humans, and a statistical significant difference was recognized in the deviation of the distribution (p=0.0002). The association of the Bm type alleles with the onset of the respiratory three disease groups (DPB, BE and PE) belonging to the COPD was shown by the comparison described above.

Any of the respiratory three disease groups (DPB, BE and PE) belonging to the COPD had a higher frequency of occurrence than that in normal humans in view of each disease (BE; p=0.012, DPB; p=0.0025 and PE; p=0.0052).

On the other hand, the frequency of occurrence of the Bm type was significantly lower than that in normal humans (p=0.049).

Frequency of observation:

Three diseases, Bm/NotBm

Bm

NotBm

Total

Normal

27

185

212

Respiratory

49

129

178

3 diseases

Total

76

314

390

Contingency table analytical statistics:

Three diseases, Bm/NotBm

Number of missing values

107

Degree of freedom

1

Chi-square value

13.494

Chi-square p value

.0002

G-square value

13.534

G-square p value

.0002

Contingency table analytical

.183

coefficient

Phi

.186

Chi-square value (Yates'

12.568

continuity correction)

Chi-square p value (Yates'

.0004

continuity correction)

Fisher's direct method p value

.0003

Contingency table analytical statistics:

DPB, Bm/NotBm

Number of missing values

227

Degree of freedom

1

Chi-square value

9.172

Chi-square p value

.0025

G-square value

8.202

G-square p value

.0042

Contingency table analytical

.181

coefficient

Phi

.184

Chi-square value (Yates'

7.997

continuity correction)

Chi-square p value (Yates'

.0047

continuity correction)

Fisher's direct method p value

.0045

Contingency table analytical statistics:

BE, Bm/NotBm

Number of missing values

209

Degree of freedom

1

Chi-square value

6.270

Chi-square p value

.0123

G-square value

5.824

G-square p value

.0158

Contingency table analytical

.146

coefficient

Phi

.148

Chi-square value (Yates'

5.389

continuity correction)

Chi-square p value (Yates'

.0203

continuity correction)

Fisher's direct method p value

.0172

Contingency table analytical statistics:

PE, Bm/NotBm

Number of missing values

241

Degree of freedom

1

Chi-square value

7.810

Chi-square p value

.0052

G-square value

6.802

G-square p value

.0091

Contingency table analytical

.172

coefficient

Phi

.175

Chi-square value (Yates'

6.587

continuity correction)

Chi-square p value (Yates'

.0103

continuity correction)

Fisher's direct method p value

.0104

Contingency table analytic statistics:

BA, Bm/NotBm

Number of missing values

221

Degree of freedom

1

Chi-square value

4.829

Chi-square p value

.0280

G-square value

6.035

G-square p value

.0140

Contingency table analytical

.131

coefficient

Phi

.132

Chi-square value (Yates' continuity

3.861

correction)

Chi-square p value (Yates'

.0494

continuity correction)

Fisher's direct method p value

.0340

Individual Classification (1)

Since the association of the Bm type among the three haplotypes with the respiratory diseases is considered as especially deep from the analytical results of the allelic classification, the classification and analysis were made of individuals without the Bm type, individuals having one Bm type (hetero) and individuals having two Bm types (homo) by particularly noticing the Bm type.

As for the respiratory three disease groups (DPB, BE and PE) belonging to the COPD, a significant difference was observed in distribution in relation to the frequency of occurrence of the haplotypic classifications Bm-0.1 and 2 based on the Bm in comparison of the normal humans with the patient groups suffering from the respiratory three diseases (p=0.0093).

A significant difference was observed in the deviation of the distribution of patients developing the DPB and PE with regard to each disease (DPB: p=0.0024 and PE: p=0.0069). There was the tendency even in the BE (p=0.089).

Frequency of observation:

Three diseases, Bm.

Bm-0

Bm-1

Bm-2

Total

Normal

79

27

0

106

Respiratory

54

29

6

89

3 diseases

Total

133

56

6

195

Contingency table analytical statistics:

DPB, Bm.

Number of missing values

123

Degree of freedom

2

Chi-square value

12.040

Chi-square p value

.0024

G-square value

.

G-square p value

.

Contingency table analytical

.286

coefficient

Cramer's V value

.299

Bm-0

Bm-1

Bm-2

Total

Frequency of observation: PE, Bm.

PE

14

6

2

22

Normal

79

27

0

106

Total

93

33

2

128

Percent (row): PE, Bm.

PE

64

27

9

100

Normal

75

25

0

100

Total

73

26

2

100

Individual Classification (2)

Analysis was made whether or not the Bm haplotype was possessed (Bm-0 vs. Bm-1.2).

As for the respiratory three disease groups (DPB, BE and PE) belonging to the COPD, the frequency of occurrence of individuals having the Bm in the respiratory three disease groups is higher than that in normal humans in comparison thereof with the normal humans, and a significant difference was observed in the deviation of distribution (p=0.039). On the other hand, there were more individuals without the Bm haplotype in BA vice versa, and a significant deviation was noted in the distribution as compared with that in the normal human group (p=0.037).

Three diseases, Bm-0/Bm-1.2

Bm-0

Bm-1.2

Total

Normal

79

27

106

Respiratory

54

35

89

3 diseases

Total

133

62

195

Frequency of observation:

BA, Bm-0/Bm-1.2

Bm-0

Bm-1.2

Total

BA

30

2

32

Normal

79

27

106

Total

109

29

138

Frequency of observation:

DPB, Bm-0/Bm-1.2

Bm-0

Bm-1.2

Total

Normal

79

27

106

DPB

17

12

29

Total

96

39

135

Percent (row): BE, Bm-0/Bm-1.2

Bm-0

Bm-1.2

Total

BE

61

39

100

Normal

75

25

100

Total

71

29

100

Contingency table analytical statistics

PE, Bm-0/Bm-1.2

Number of missing values

130

Degree of freedom

1

Chi-square value

1.088

Chi-square p value

.2969

G-square value

1.040

G-square p value

.3079

Contingency table analytical

.092

coefficient

Phi

.092

Chi-square value (Yates'

.609

continuity correction)

Chi-square p value (Yates'

4.353

continuity correction)

Fisher's direct method p value

.3035

Individual Classification (3)

Furthermore, a comparison of the frequency of occurrence (Bm-0.1 vs. Bm-2) was made between individuals having the Bm haplotype as the homo (BBmm; Bm-2) and individuals without the haplotype (Bm-0.1). As for the respiratory three disease groups (DPB, BE and PE) belonging to the COPD, a significant difference was observed in the frequency of occurrence between the individuals having the Bm haplotype as the homo (BBmm) and individuals without the Bm haplotype in comparison of the respiratory three disease groups with the normal humans (p=0.021), and all the six individuals having the Bm homo type (Bm-2) were affected by any of the respiratory three diseases (DPE, BE and PE) belonging to the COPD. Three individuals were affected by the DPB and one thereof was affected by the BE. No human having the Bm homo type (Bm-2) was found in 106 normal humans and 32 patients suffering from the BA.

As for each disease, a statistical significant difference was observed in the deviation of the distribution of patients suffering from the DPB and PE (DPB: p=0.0082 and PE: p=0.029).

Frequency of observation:

Three diseases, Bm-0.1/Bm-2

Bm-0.1

Bm-2

Total

Normal

106

0

106

Respiratory

83

6

89

3 diseases

Total

189

6

195

Frequency of observation:

DPB, Bm-0.1/Bm-2

Bm-0.1

Bm-2

Total

Normal

106

0

106

DPB

26

3

29

Total

132

3

135

Percent (row):

PE, Bm-0.1/Bm-2

Bm-0.1

Bm-2

Total

PE

91

9

100

Normal

100

0

100

Total

98

2

100

Contingency table analytical statistics:

BE, Bm-0.1/Bm-2

Number of missing values

114

Degree of freedom

1

Chi-square value

2.809

Chi-square p value

.0937

G-square value

.

G-square p value

.

Contingency table analytical

.138

coefficient

Phi

.140

Chi-square value (Yates'

.289

continuity correction)

Chi-square p value (Yates'

.5909

continuity correction)

Fisher's direct method p value

.2639

The above results definitely show that the Bm type haplotypes are associated with chronic respiratory tract inflammations in respiratory diseases according to a certain mechanism by analyzing the intron genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract. Furthermore, it is also shown that the association of the human trypsin-like enzyme of the respiratory tract with diseases is different between the three diseases of DPB, BE and PE belonging to the chronic obstructive pulmonary diseases (COPD) and the BA.

Since all the individuals having a certain genetic polymorphism do not develop some diseases, the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract are not a decisive onset factor such as the so-called genetic disease and may safely be said as a readily onsetting factor. That is, when an environmental factor or the like is added to individuals having the Bm haplotypes, the individuals are susceptible to the onset of the respiratory diseases such as the BE, PE and DPB.

It is shown from the above results that diseases associated with the human trypsin-like enzyme of the respiratory tract can be classified by using the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract. The analytical method for the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract is a means applicable to the prediction of onset constitution of diseases associated with the human trypsin-like enzyme of the respiratory tract in individual humans, the prediction of effects on the treatment of the diseases, prediction of the possibility for relapse of the prognosis thereof or the like.

POSSIBILITY OF INDUSTRIAL UTILIZATION

The present invention provides a method for determining the disease-associated constitution of individual humans by the analyzing the genetic polymorphisms of the human trypsin-like enzyme of the respiratory tract. Accordingly, when the diseases associated with the human trypsin-like enzyme of the respiratory tract can be identified by the analysis, it can be assumed that individuals having the certain genotype of the human trypsin-like enzyme of the respiratory tract are susceptible to some diseases.

That is, information about the methods of treatment for the individual humans can be provided in an early stage by predicting the disease onset constitution (individuals having the constitution susceptible to certain diseases) and related with early diagnosis and early treatment. The possibility for the relapse of the diseases can be estimated even after the treatment. That is, physicians can pay careful attention to patients and provide proper direction by predicting the prognosis of the treatment (the course of curing after the treatment of patients and risk of relapse)

Furthermore, the genetic polymorphic analysis of the human trypsin-like enzyme of the respiratory tract has a possibility for providing a means for determining effects of drugs to be administered and narrowing the patient groups in which the administered drugs are effective in the development of the drugs in the morbid state associated with the human trypsin-like enzyme of the respiratory tract.

As described above, the early diagnosis, early treatment and direction of proper prophylactic methods, appropriate medication and proper after follow after the treatment are related to a reduction in huge medical expenditures causing problems at present.

17

1

107

DNA

Homo sapiens

1
gtgaggccac cactacctac ccatctggga acaattagaa tagacaggtc atgaagactg 60
caccctctac cctaggattg aattgagcca gaaataattc aatgcaa 107

2

150

DNA

Homo sapiens

2
taaactcact tgccagctat aatgcaggaa atatagcaag agatgtggat ccaatagttc 60
tagatagtgg tacaggatgg ctaagatgaa ttatatatct gaaatgttca caaattccct 120
actcatatag catgtttcat aatgttttag 150

3

163

DNA

Homo sapiens

3
gtaagtgtct cggaaaaaaa aattaacaat agaaatgtct tatatttgct attaggtaat 60
tttttaaatt aggaaacatc tggaataggt gtttctattc ttctacagac agaaccattc 120
tatattctgc tcagcccaag ctctggctac ccctgagtct cct 163

4

177

DNA

Homo sapiens

4
tcctcatcta cttggggaat tttggctgcg aagaaactcc aaagtaaatc tttagaagcc 60
ttcattgtta aatatgaaat aatgtttgga gtacatttat ttcttctcaa atttattata 120
gggtcaataa tgtacacatc ttgaagtcca tttttttcct gcttttataa caaacag 177

5

120

DNA

Homo sapiens

5
gtaagctcaa gacaatctca tccatgtcat catccaagaa gtgtataagc acttcctagt 60
atgtgataat gtgatagaca taagtgtaac agttacaata cacagccctg ttcctctaaa 120

6

125

DNA

Homo sapiens

6
ggaaataggc tgactttatt tgtataatga atgtgactcc ttcctcgact gccatagaaa 60
taaactcctt aatattttgg gtttgtcttt gcacttaagt aatcagtcat tctgtttttt 120
tacag 125

7

35

DNA

Artificial Sequence

Description of Artificial Sequence primer A1

7
aagtcagtct gcggctcaat aatgcccacc actgt 35

8

35

DNA

Artificial Sequence

Description of Artificial Sequence primer A2

8
ctcattctta gtttaggaaa tgttgtggaa atacc 35

9

35

DNA

Artificial Sequence

Description of Artificial Sequence primer B1

9
acccagaata ttccacctgg ctctactgct tatgt 35

10

35

DNA

Artificial Sequence

Description of Artificial Sequence primer B2

10
cattacttat tattctgacc tgtccttgcc ttagc 35

11

35

DNA

Artificial Sequence

Description of Artificial Sequence primer C1

11
ggagccatct tgtctggaat gctgtgtgct ggagt 35

12

35

DNA

Artificial Sequence

Description of Artificial Sequence primer C2

12
cacaataaac caaagccgcc gtgagtcttc ttgta 35

13

35

DNA

Artificial Sequence

Description of Artificial Sequence primer D1

13
tgtcgtcgca ggggtagtga tcctggcagt cacca 35

14

35

DNA

Artificial Sequence

Description of Artificial Sequence primer D2

14
ttcaattctt ccactcaaag tcctgtattc ctgtg 35

15

35

DNA

Artificial Sequence

Description of Artificial Sequence primer E1

15
tgaggcaaga tggtagtggt gtgagagcgg atgtt 35

16

35

DNA

Artificial Sequence

Description of Artificial Sequence primer E2

16
ggccagcttc cctcctcagc ctcagtgcct ccaag 35

17

3376

DNA

Homo sapiens

17
gaattcggct tggagccatc ttgtctggaa tgctgtgtgc tggagtacct caaggtggag 60
tggacgcatg tcaggtaagc tcaagacaat ctcatccatg tcatcatcca agaagtgtat 120
aagcacttcc tagtatgtga taatgtgata gacataagtg taacagttac aatacacagc 180
cctgttcctc taaaatttat aatctagatt ttagaaataa atttttttat gaatgaagtt 240
tatctatcat gaaagcatta actctgagag gccaaattac agagtagtta accatccaaa 300
gctcaagaat cagaaagacc tcgatttgaa ttccttaacc tctattacca agtctcttta 360
actaaaagct ggggataatc ataatagcac ctaacttttt gggtactaag aaaagttaaa 420
tgaagactaa atatatcagg cacatggtaa acaacaaaga aatctcatct atttcactat 480
tattaatgta gaccatggtc actcgtgtta ataactttaa cctcaacctt ttaactgcta 540
tgaaggatta aataaaaaat taatcactat attataaaaa ttaattgata tataataaat 600
gaatttaaga aatacgtaat aattcatgga ctccttgaag atagaaaatt tatacaaaat 660
cctagtaatt tgagtcacaa aagctcctac aataatgaaa cagtatgaat gaaaaagaaa 720
agaaataact attatatttg gatctagccc ataattttta accaaatgca caaaaacaaa 780
caacaaatat gaaattctca ctgtaaagtg attaaaatca aatttgaatt ctaaaatttt 840
aaattaaatt atctaaacat aattgatgca gttatatgtt ttaataggtt ttgttcacat 900
atctgaaatc caactccaca tagtagcagg aacagctggt gtcagaaatt aaatattctt 960
ttagtctgga gttttaaaaa atcaatctgt ttacttgagt aatttgttgc tgttttcatg 1020
ggtgaattgt atacagaagg ataggaatta ttcttcgcat caaaaggtca ctgactttca 1080
tatttagtgc tcatggtctt taaaaaatgg ataaaaagta gttctcacat ttcatggaaa 1140
gcccccaatc catgagcaca tttcccaaaa ttgaaacatt tttatcaact gcaagttgtg 1200
tgtaggtgga gatttgtttt tcaattgtca agatactgtt aattacccag tcctttatct 1260
ccttttggtg gagatgtctc tgtgctagga aacccttctt gctctccttc ctgtttctct 1320
tttactactg gccctgaaac aacaaattct caagtttcat gacagctttc caaagaatcc 1380
atcaatcaaa taagcaacac aactcgacac tgacaattcc agacctacta agagcattaa 1440
ttaagactta aaaataaaca tgagttttaa aagggtgtta ttcattattt tcccatttat 1500
aacgtccctt accttctgtc cttcagtgca tacaaattat tatcttcctt gaagcccagt 1560
tcaagccgta cctcaccatg ataccttcca tgtatattcc actccaggcc tcactgattt 1620
ttaactgaaa tactataatg catagttcac aattaaaaaa aaaaaaaaca cagcacttta 1680
cataagagct tacaggatcc tatttgtttt atccattctt ttgttcattt ttacaatcat 1740
taattcaaag gaattatatt aattactttc tatgcacccg acgttgtgtt aacacaacaa 1800
tactatccct gcattcagca agtctatggt ctacaagaga ggacacaaat tcaaatgtct 1860
gtagtcaagc agtgaagctg gctagatatg gaaaaattac aagtccctct tgctttaaca 1920
tttgcttgcc cacatttgat cagacatcat gcaaaataat ttctcactat agagaaaaaa 1980
acactacaaa accaataata taaagaactg agaactggtt tactgaagca tgcatatgtc 2040
atctaaaaga agcaggtgac gaccagcttc atgaagtact tgccatgcat attggcactt 2100
cacacactga cccttctccc cacctagacc agtaattaaa caggtatgga tgagctagct 2160
actaagagca gccaactgaa tagctgacta atttagaagc acacttggta ataatagctg 2220
acttttatta gtactgacta tactatatgc taagctgtac tcaaagtgct ttgagtttta 2280
aactgataca aacattatat gaggaaacag aggtacagag agctattcac cagcttacca 2340
aaggtcacat agctggtaag tggaggactt aaacccagac tatctagttt cagaacgcgc 2400
agacttaatc catcgtgcag aacataagac atactccatc tgtctcccca actaggttat 2460
tatgtgcaca aatatttatt ggttggttgg ttcattatta tgactgggtg gtaagtatgt 2520
cattaggagt gttttgctta tgactatata aatttcttca ccaaaagaag actttctgat 2580
gatatactat gcatcagaca ccacgcaggg tgctaaggtt aggaagataa gtgagacttc 2640
tagaaactca ttcattcaac aaatatctcc taagggctag aagcttaggt ttcagcagtg 2700
aacagaatag gtatgttctc tttcgtgttg gaccttatag tatatctggg aaaacagaca 2760
ttgaataaat atcacaaatg caagtgagtg tttcagagac atgcagctgc tacatcaaac 2820
caaaacagaa caaaacaaac aacccaaaaa ctgaccagtg ggattaagtg taaataggca 2880
cacaaatgca caaatatgct tttataaaat agtgaagcag tgacagagac acacacaaga 2940
tataaagaca caatgaagaa caattgagcc caaagctgga aagggtgaga gtgtgaagga 3000
aaaaggttga tcagagaagt tttcccgaag gagagaaagc ctggatgatt aggaggcaac 3060
cactcggtga ctgagggaaa tctgaaaaat gtatttgtca tcttctcaga cttgctgaag 3120
gaatgacttg ggtactttga ggatttcagt aatttttcca tgacttggta taatatttca 3180
aaaggaaata ggctgacttt atttgtataa tgaatgtgac tccttcctcg actgccatag 3240
aaataaactc cttaatattt tgggtttgtc tttgcactta agtaatcagt cattctgttt 3300
ttttacaggg tgactctggt ggcccactag tacaagaaga ctcacggcgg ctttggttta 3360
ttgtgaagcc gaattc 3376

Number	Date	Country
7-67640	Mar 1995	JP
8-89206	Apr 1996	JP

Analysis of predisposition based on human airway trypsin protease gene polymorphism

Information

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Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

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US

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Abstract

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Priority Claims (1)

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Non-Patent Literature Citations (6)