Patent Application
20090320164
The present invention relates to a production process of a plant cell in which one or more chromosomes are disappeared.
In multicellular organisms, the chromosome number in somatic cells can usually be expressed as 2n. In response to these normal organisms, somatic cells and individual organisms with their chromosome numbers altered are referred to as aneuploid cells or aneuploid individual organisms, or simply aneuploids, which are extremely important in breeding and genetics.
Specifically, most of these aneuploids indicate characteristics different from those of normal organisms and thus naturally-occurring or artificially-produced aneuploids of vegetables, flowers and ornamental plants and others are used as materials for further breeding, or are used as new varieties in themselves.
Among the aneuploids, in monosomics with only one chromosome disappeared, a gene locus on the disappeared chromosome does not indicate a normal segregation ratio in F1 generation, obtained by autologous hybridization, and thus, by using this, the gene locus can be determined. This technique is called monosomic analysis; for example, a series of monosomics covering all 21 pairs of chromosomes of bread wheat (Chinese Spring) was produced, and gene loci associated with many characteristics were determined through studies on characteristics of these monosomics and their self-fertilized F1 generations (on-patent document 1).
However, generation of aneuploids is very difficult. For example, the monosomic series of bread wheat was produced using the haploids obtained by crossbreeding rye and bread wheat; however, species whose monosomics can be obtained by this technique is extremely limited. On the other hand, aneuploids such as monosomics can also be obtained by exposing cells of the organisms to chemical substances such as colchicine and EMS (ethylmethane sulphonate) or radiation (Non-patent document 2); however, use of these methods requires advanced techniques and often produces unexpected damage to other chromosomes which are not to be disappeared.
Non-patent document 1: Sears, Univ. Missouri Res. Bull. (US), 572: 1-58 (1954)
Non-patent document 2: Yasuo Ukai, Plant Breeding, pp. 259-261 (2003)
The inventors performed a keen examination regarding the task of providing a simple aneuploid production process, applicable to all species, without producing unexpected damage to other chromosomes which were not to be disappeared and as a result, found that this could be resolved by use of a site-specific recombination system and achieved the present invention.
Specifically, the present invention relates to the following (1)-(14);
(1) A process for producing a plant cell in which one or more chromosomes are disappeared said process comprises the following steps (A)-(C) (hereinafter, referred to as the first embodiment of the present invention);
(A) introducing a vector comprising
two site-specific recombinase recognition sequences oriented in the opposite direction and
a site-specific recombinase gene which is positioned inside or outside of the region between the two site-specific recombinase recognition sequences and which encodes a site-specific recombinase which recognizes the two site-specific recombinase recognition sequences,
into a plant cell;
(B) culturing and growing the vector-introduced plant cell (A); and
(C) selecting a cell in which a predetermined chromosome is disappeared, from the cell grown in (B).
(2) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (1),
wherein a vector comprising an additional negative selectable marker gene, positioned inside or outside of the region between the two site-specific recombinase recognition sequences oriented in the opposite direction) is used as a vector in the step (A), and
wherein the plant cell is cultured under conditions where the negative selectable marker gene functions in the step (B)
(3) A process for producing a plant cell in which one or more chromosomes are disappeared, said process comprising the following steps (A)-(C) (hereinafter, referred to as the second embodiment of the present invention);
(A) introducing a vector comprising
one site-specific recombinase recognition sequence comprising a point-symmetric nucleotide sequence, and
a site-specific recombinase gene encoding a site-specific recombinase which recognizes the site-specific recombinase recognition sequence,
into a plant cell;
(B) culturing and growing the vector-introduced plant cell in (A); and
(C) selecting a cell in which a predetermined chromosome is disappeared, from the cell grown in (B).
(4) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (3),
wherein a vector comprising an additional negative selectable marker gene is used as a vector in the step (A), and
wherein a plant cell is cultured under conditions where the negative selectable marker gene functions in the step (B).
(5) A process for producing a plant cell in which one or more chromosomes are disappeared, said process comprises the following steps (A)-(D) (hereinafter, referred to as the third embodiment of the present invention):
(A) introducing a vector comprising two site-specific recombinase recognition sequences oriented in the opposite direction, or one site-specific recombinase recognition sequence comprising a point-symmetric nucleotide sequence, into a plant cell;
(B) culturing the vector-introduced plant cell in (A) and allowing the site-specific recombinase which recognizes the two site-specific recombinase recognition sequences to act transiently in the cell during at least growth of the cell;
(C) culturing and growing a cell in which the site-specific recombinase has been allowed to act in (B); and
(D) selecting a cell in which a predetermined chromosome is disappeared, from the cell grown in (C).
(6) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (5),
wherein a vector comprising two site-specific recombinase recognition sequences oriented in the opposite direction, and a negative selectable marker gene positioned inside or outside of the region between the two site-specific recombinase recognition sequences, or a vector comprising one site-specific recombinase recognition sequence comprising a point-symmetric nucleotide sequence, and a negative selectable marker gene is used in the step (A), and
wherein the plant cell is cultured under conditions where the negative selectable marker gene functions in the step (C).
(7) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (5), wherein the site-specific recombinase is allowed to act transiently by introducing the site-specific recombinase into the cultured plant cell in the step (B).
(8) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (5), wherein the site-specific recombinase is allowed to act transiently by introducing a site-specific; recombinase gene encoding the site-specific recombinase into the cultured plant cell in the step (B).
(9) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (8), wherein introduction of the site-specific recombinase gene is carried out by introducing a vector comprising a site-specific recombinase gene and a negative selectable marker gene, into a plant cell
(10) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (8),
wherein the site-specific recombinase gene is positioned between the two site-specific recombinase recognition sequences, oriented in the same direction, which are recognized by the site-specific recombinase encoded by the site-specific recombinase genes in a vector, and
the vector is introduced into a plant cell,
(11) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (10), wherein a negative selectable marker gene, together with a site-specific recombinase gene, is positioned between the two site-specific recombinase recognition sequences, oriented in the same direction, in the vector.
(12) The process for producing a plant cell in which one or more chromosomes are disappeared according to the above (2), (4), (6), (9) or (11), wherein a lethal induction gene or a morphological abnormality induction gene is used as the negative selectable marker gene,
(13) A plant cell in which one or more chromosomes are disappeared, which is obtainable by the process according to the above (1)-(12).
(14) A plant tissue or a plant comprising the plant cell according; the above (13)
According to the present invention, plant cells in which one or more chromosomes are disappeared can be produced regardless of species.
In order to produce them, it is sufficient to use only very general techniques as a gene transfer technique for a plant or a plant tissue culture technique. The vector used here for gene introduction has a very simple construction
In the present invention, a plant individual can be reproduced from plant cells in which one or more chromosomes are disappeared without proceeding through reproductive cells.
Thus, the present invention can be applied to all plant species, and provides a simple production process of monosomics such as aneuploids like, i.e., aneuploid plant cells or plant individual which are important in breeding or genetics.
In addition, generation of the aneuploids never causes unexpected damage to chromosomes other than ones which are to be disappeared.
First, details of the first embodiment of the present invention is described.
In the first embodiment of the present invention, first of all, a vector comprising two site-specific recombinase recognition sequences (hereinafter, also simply referred to as a recognition sequence), oriented in the opposite direction, and a site-specific recombinase gene (hereinafter) also simply referred to as a recombinase gene) encoding a site-specific recombinase (hereinafter, also simply referred to as a recombinase) which recognizes the recognition sequence, positioned inside or outside of the region between the two recognition sequences, is introduced into a plant cell.
The recognition sequence of a site-specific recombinase is a DNA factor having a predetermined nucleotide sequence; in a site-specific recombination system, the site-specific recombinase recognizes the recognition sequence to exert various functions. For example, when there are two regions between two recognition sequences of the same nucleotide sequence on a DNA molecule (X-X′) positioned in the opposite direction (i.e., recognition sequences oriented in the opposite direction, in the present invention), recombination occurs in the regions between these X-X′ regions through the function of the recombinase regardless of whether these two regions exist on the same DNA molecule or on different DNA molecules separately. In the present invention, the function is used.
As known site-specific recombination systems, the combinations of recognition sequences and recombinases which recognize them to exert functions include the Cre/lox system R/RS system, FLP/FRT system, cer system and fim system isolated from microorganisms such as phage, bacteria (E. coli, etc.) and yeast (for review of article, N. L. Craig, Annu. Rev. Genet., 22: 17 (1988)). No site-specific recombination system in higher organisms is known yet, however, it has been demonstrated that the recognition sequences and recombinases of the site-specific recombination systems, isolated from the above-described microorganisms, behave in the same manner as in the original organisms, even if introduced into organism species other than those from which the systems derived, i.e., plants and animals.
The recognition sequence and recombinase gene used in the present invention can be selected arbitrarily from combinations of these recognition sequences and genes encoding a recombinase which recognizes them to function. In particular, the Cre/lox system and G system are widely used in animals, plants, etc., showing high recombination efficiency, and therefore are preferable as combinations of recognition sequences and recombinase genes used in the present invention. Mutated types (i.e., wild type recognition sequences with artificial or natural partial modifications) can also be used as recognition sequences. However, the mutated recognition sequences in this case should be recognizable by the recombinase encoded by the recombinase gene which coexists in the above-described vector.
In addition, the present invention allows more efficient isolation of cells in which chromosomes are disappeared with use of a negative selectable marker gene. Specifically, the negative selectable marker gene can be used by being positioned inside or outside of the region between the recognition sequences of the above-described vector. Here, the positional relationship with the recombinase gene makes no difference. Specifically, the negative selectable marker gene can be positioned inside or outside of the recognition sequence together with recombinase gene, or the recombinase gene can be positioned inside and the negative selectable marker gene can be positioned outside, or vice versa.
Any genes whose expression inhibits normal growth and differentiation of host cells can be used as a negative selectable marker gene. Such genes include lethal induction genes and morphological abnormality induction genes.
The lethal induction genes indicate overall genes whose expression impairs the functions of host cells and leads to death; for example, genes encoding RNAse, DAM methylase, cytosine deaminase (codA), diphtheria toxin, Bax and so forth are widely known. The morphological abnormality induction genes indicate overall genes whose expression disrupts the directions of host cell growth and differentiation and causes morphological differentiation out of the ordinary Plant hormone-associated genes such as plant hormone synthesis genes and plant hormone signal transduction genes which cause growth retardation of a host plant, loss of apical dominance, change of pigment, crown gall, callus induction, hairy root, rippling leaves and so forth can be used as the morphological abnormality induction genes.
The plant hormone synthesis genes are genes which encode proteins involved in the plant hormone synthesis [e.g., ipt (isopentenyltransferase) gene of plant pathogens such as Agrobacterium (A. C Srigocki, L. D. Owens, Proc. Natl. Acad. Sci. USA, 85: 5131 (1988)), iaaM (tryptophan monooxygenase) gene (H. J. Klee et al., GENES & DEVELOPMENT, 1: 86 (1987)), gene 5 gene (H. Kerber et al., EMBO Journal, 10: 3983 (1991)), gene 6b gene (P. J. J. Hooyaas et al., Plant Mol. Biol., 11: 791 (1988)), rol gene groups such as rolA to rolD (F. F. White et al., J. Bacteriol, 164: 33 (1985)), iaaL (indoleacetic acid-lysine synthetase) gene of Pseudomonas syringae subsp. savastnoi (A. Spena et al., Mol. Gen. Genet., 227: 205 (1991)), and in addition, homeobox genes, phytochrome genes and so forth of various plants].
Plant hormone signal transduction genes are genes which encode proteins of sensors which recognize the existence of plant hormones such as gibberellin, ethylene, auxin and cytokinin or proteins involved in a series of signal transduction pathways from the sensors, [e.g., ETR1 gene (ethylene receptor gene) (C. Chawg et al., Science, 262: 539 (1993)), CKI1 gene (cytokinin receptor gene) (T. Kakimoto, Science, 274: 982 (1996) and variants thereof (e.g., CKI2 gene), GCR1 gene (S. Plakidou-Dymock et al., Current Biology, 8: 315 (1988)), IBC6 gene and LBC7 gene (1 Brandstatter, J. J Kieber, The Plant Cell, 10: 1009 (1988))].
Among these morphological abnormality induction genes, the ipt gene which causes loss of apical dominance and rol genes which cause formation of hairy root, growth retardation of a plant reproduced from hairy root rippling leaves and so forth induce characteristic morphological abnormalities to inhibit redifferentiation of a plant individual and are therefore particularly preferable as the morphological abnormality induction genes used in the present invention.
The method for introducing the vector of the present invention into a plant cell includes direct and indirect introducing methods; physical or chemical methods such as microinjection, electroporation, polyethylene glycol method, fusion method, and high-speed ballistic penetration method can be used as direct introducing methods, and techniques with viruses and bacteria which infect plants can be used as indirect introducing methods (I. Potrykus, Annu. Rev. Plant Physiol. Plant Mol. Biol., 42: 205 (1991)). Among the viruses and bacteria used for the indirect introducing methods, viruses include cauliflower mosaic virus, geminivirus, tobacco mosaic virus and brome mosaic virus, and representative bacteria include Agobacteriun tumefaciens (hereinafter, abbreviated as A. tumefaciens) and Agrobacterium rhizogenes.
The vector-introduced plant cells can be cultured and grown under heretofore known culturing and environmental conditions most suitable for plant cells. Cells in which one or more chromosomes are disappeared are produced among grown cells, and DNA analysis on the cells obtained from cultured tissue after growth allows selection of cells with target chromosomes disappeared or tissues containing the cells. Here, the heretofore known techniques such as PCR and Southern blotting can be used as techniques for the DNA analysis. When a vector comprising a negative selectable marker gene is used as the vector, cells in which chromosomes are disappeared can be selectively obtained by culturing vector-introduced plant cells under conditions where the negative selectable marker gene inhibits the normal growth and differentiation of cells having this on chromosomes (in the present invention, these conditions are referred to as conditions where a negative selectable marker gene functions).
Next, the second embodiment of the present invention is described in detail.
In the second embodiment of the present invention, a vector comprising one site-specific recombinase recognition sequence comprising a point-symmetric nucleotide sequence, and a site-specific recombinase gene encoding a site-specific recombinase which recognizes the site-specific recombinase recognition sequence is used as the vector to be introduced into a plant cell.
Here, the site-specific recombinase recognition sequence comprising a point-symmetric nucleotide sequence is a DNA factor with a so-called palindromic sequence in which a predetermined nucleotide sequence is arranged in a point-symmetric manner. This recognition sequence comprising a point-symmetric nucleotide sequence is the same as the recognition sequence used in the first embodiment of the present invention in that it functions in combination with the recombinase which recognizes this recognition sequence to function, but is different in that two copies of this recognition sequence simply exist on a DNA molecule and recombination of the DNA molecule occurs via the function of the recombinase regardless of whether they exist on the same DNA molecule or different DNA molecules. Recognition sequence LoxPsym which functions in combination with the recombinase of the Cre/lox system is known as the recognition sequence comprising a point-symmetric nucleotide sequence (Ronald H. Hoess et al., Nucleic Acid Res., 11: 14(5): 2287-2300 (1986)).
Also, in the present invention, a negative selectable marker gene can be used in the same manner as in the first embodiment of the present invention to further improve the efficiency of obtaining cells in which chromosomes are disappeared. For this purpose, this negative selectable marker gene is positioned in the above-described vector together with the recognition sequence comprising the above point-symmetric nucleotide sequence and recombinase gene. Here, the positional relationship with the recognition sequence or recombinase gene makes no difference. As the negative selectable marker gene, the negative selectable marker gene in the first embodiment of the present invention, described above, can also be used in the present invention in the same manner.
As the items other than those specifically described, the present invention can be conducted in the same manner as in the first embodiment of the present invention. Specifically, the vector of the present invention can be introduced into a plant cell in the same manner as in the first embodiment of the present invention and the plant cells to which the vector of the present invention was introduced are cultured and grown to produce cells in which one or more chromosomes are disappeared, and these cells can be selected in the same manner as in the first embodiment of the present invention.
Furthermore, the third embodiment of the present invention is described in detail.
In the third embodiment of the present invention, first of all, a vector comprising two site-specific recombinase recognition sequences, oriented in the opposite direction or one site-specific recombinase recognition sequence comprising a point-symmetric nucleotide sequences is used as a vector to be introduced into a plant cell (hereinafter, this vector is also referred to as a vector for introduction of a recognition sequence). Unlike in the vectors in the first and second embodiments of the present invention a recombinase gene encoding a recombinase which recognizes these recognition sequences is not positioned in this vector.
On the other hand, a negative selectable marker gene can also be positioned in this vector together with these recognition sequences in the same manner as in the vectors in the first and second embodiments of the present invention to further improve the efficiency of obtaining cells in which chromosomes are disappeared. In order to position this negative selectable marker gene together with two recognition sequences oriented in the opposite direction this negative selectable marker gene can be positioned inside or outside of the region between the recognition sequences. In order to position this negative selectable marker gene together with one recognition sequence comprising a point-symmetric nucleotide sequence, this negative selectable marker gene can be positioned regardless of its positional relationship.
In the present invention, after introduction of the above-described vector into a plant cell, the recombinase which recognizes the recognition sequence positioned in this vector is allowed to act transiently in the cells during at least growth of the cells.
In order to allow the recombinase to act at least transiently in growing plant cells, for example, the recombinase itself or a recombinase gene encoding his recombinase is introduced into the growing plant cells) and/or after introduction into the plant cells, the plant cells are grown.
As the introduction of the recombinase gene, the recombinase can be allowed to act transiently in the cells only by positioning this recombinase gene in an appropriate vector to be introduced into a plant cell (hereinafter, the vector used for the introduction of the recombinase gene into a plant cell after introduction of the recognition sequence is also referred to as a vector for introduction of a recombinase gene). This is because the recombinase gene introduced into a plant cell is expressed without being incorporated into the chromosomes, and the free recombinase gene disappears after producing the recombinase to some extent and stops production of the recombinase in the cells, to thereby allow this recombinase to act transiently.
However, in order to ensure such transient action of the recombinase, the recombinase gene between two recognition sequences comprising the same nucleotide sequence, oriented in the same direction, and recognized by the recombinase that this recombinase gene encoded (i.e., recognition sequence oriented in the same direction, in the present invention), is positioned in a vector to be introduced into the plant cells. The recombinase gene, thus introduced into the plant cells, is incorporated and expressed in a state of being flanked by the above two recognition sequences even if incorporated into the chromosomes of the plant cells; thus, after producing the recombinase to some extent in the cells, gene is removed and freed from the chromosomes, and then disappeared by the function of recombinase produced by the gene itself.
When the recombinase is allowed to act transiently in the cells by introducing the recombinase gene into the plant cells, cells in which the recombinase has been allowed to act transiently can reliably be obtained from cells, to which the recombinase gene is introduced, by introducing a negative selectable marker gene into the plant cells together with the recombinase gene. As the negative selectable marker gene, the negative selectable marker gene used in the above-described first and second embodiments of the present invention can be used in the same manner also in the present invention.
In the above case, a negative selectable marker gene is introduced into a plant cell, together with a recombinase gene, only by positioning this recombinase gene and negative selectable marker gene in a vector and introducing the vector into the plant cells. In order to position a recombinase gene between two recognition sequences oriented in the same direction in a vector, a negative selectable marker gene is positioned, together with the recombinase gene, between two recognition sequences oriented in the same direction in the vector.
When the recombinase gene is introduced into a plant cell to which the recombinant enzyme has been allowed to act transiently in the cells, it is preferred to introduce an additional selectable marker gene into the plant cells together with the recombinase gene. Specifically, in the same manner as in the negative selectable marker gene described above, a selectable marker gene is positioned in a vector together with the recombinase gene, or with the recombinase gene and negative selectable marker gene, and this vector is introduced into the plant cells. In this case, positioning, type, the number and so forth of the selectable marker gene are not particularly limited. For example, when the recombinase gene is positioned between two recognition sequences oriented in the same direction, the selectable marker gene can be positioned inside or outside of the region between the recognition sequences, or can be positioned with the region between the recognition sequences existing as an obstacle between the promoter region and structural gene region of the selectable marker gene so that disappearance of the recombinase gene results in the expression of the selectable marker gene.
One or more heretofore known selectable marker genes, including the neomycin phosphotransferase (NPTII) gene which confers kanamycin resistance to plants, antibiotic resistance genes such as the hygromycin phosphotransferase gene which confers hygromycin resistance to plants and herbicide tolerance genes such as the phosphinothricin acetyltransferase (bar) gene which confers bialaphos resistance, can be used as selectable marker genes. Thus, introducing a selectable marker gene into a plant cell together with a recombinase gene allows selective growth of cells to which a recombinase gene was introduced.
The plant cells, to which a recombinase or recombinase gene encoding a recombinase is introduced, and in which this recombinase has been allowed to act transiently during growth, can be cultured and grown under the heretofore known culturing and environmental conditions most suitable for plant cells. Cells in which one or more chromosomes are disappeared are produced among grown cells, and DNA analysis on the cells obtained from cultured tissue after growth allows selection of cells with target chromosomes disappeared or tissues containing the cells. When a vector comprising a negative selectable marker gene is used as the vector for introduction of a recognition sequence or recombinase gene, cells in which chromosomes are disappeared and/or cells in which a recombinase has been allowed to act transiently can be selectively obtained by culturing the plant cells, into which the vector for introduction of the recombinase gene is introduced, under conditions where the negative selectable marker gene functions.
As items other than those specifically described, the present invention can be conducted in the same manner as in the first or second embodiment of the present invention. Specifically, in the present invention, the recognition sequence and recombinase gene used in the vector in the first embodiment of the present invention can be used as two recognition sequences oriented in the same or opposite direction and recombinase gene encoding a recombinase which recognizes the sequences to exert function; the recognition sequence and recombinase gene used in the vector in the second embodiment of the present invention can be used as a recognition sequence comprising a point-symmetric nucleotide sequence and recombinase gene encoding a recombinase which recognizes this to exert function. The vector for introduction of a recognition sequence and the vector for introduction of a recombinase gene can be introduced into a plant cell in the same manner as in the first embodiment of the present invention, and the plant cells to which the vector for introduction of a recognition sequence can be cultured in the same manner as in the first embodiment of the present invention.
In the cells for which two recognition sequences oriented in the opposite direction are introduced into chromosomes, the chromosomes are replicated and duplicated as somatic cell division (mitosis) starts. At this time, if the recombinase functions, DNA recombination may occur in the regions between two recognition sequences, which exist on each of these two chromosomes produced by duplication.
When this recombination occurs symmetrically, there is no substantial change in both chromosomes after recombination. However, when this recombination occurs asymmetrically, one chromosome having two centromeres in a point-symmetric position (dicentric chromosome) and one chromosome without centromere (acentric chromosome) are produced after recombination. In normal somatic cell division, the duplicated chromosomes move to both poles of the spindle fibers which are subsequently produced, and are divided while moving along the spindle fibers to be chromosomes of newly-produced daughter cells, however, the dicentric chromosome and acentric chromosome cannot move along the spindle fibers and therefore cannot be divided into daughter cells. Thus, both daughter cells which are produced after somatic cell division at this time lose the corresponding chromosomes (
The same phenomenon also occurs in cells to which one recognition sequence comprising a point-symmetric nucleotide sequence is introduced into chromosomes. This is because when a recognition sequence comprising a point-symmetric nucleotide sequence is introduced into chromosomes, DNA recombination occurs between the recognition sequences which exist on each of the two chromosomes produced by duplication, and also in this case, as a result of asymmetric recombination, the dicentric chromosome and acentric chromosome are produced all the same (
As a result of keen examination, the inventors made the above finding and achieved the first, second and third embodiments of the present invention.
Specifically, in the first embodiment of the present invention, a vector comprising two recognition sequences oriented in the opposite direction and a recombinase gene encoding a recombinase which recognizes the recognition sequence, positioned inside or outside of the region between the two recognition sequences, is introduced into a plant cell, and these cells are cultured and grown.
If two recognition sequences oriented in the opposite direction and a recombinase gene encoding a recombinase which recognizes the recognition sequence are introduced into the chromosomes of these plant cells by introduction of the above-described vectors into a plant cell, two chromosomes with the same structure introduced are produced after somatic cell division starts during the growth of these plant cells. At this time, the functions of the recombinase produced by the expression of the recombinase gene on the chromosomes cause a DNA recombination in the regions between the two recognition sequences which exist on these two chromosomes, and as a result, a dicentric chromosome and acentric chromosome are produced to generate daughter cells in which chromosomes are disappeared (
In the second embodiment of the present invention, a vector comprising one recognition sequence comprising a point-symmetric nucleotide sequence and a recombinase gene encoding a recombinase which recognizes the recognition sequence is introduced into a plant cell, and these cells are cultured and grown.
Also, in this case, daughter cells in which chromosomes are disappeared are produced in the same manner as in the first embodiment of the present invention. One different point from the case in the first embodiment of the present invention is that DNA recombination occurs between two recognition sequences which exist on each of the duplicated two chromosomes (
In the third embodiment of the present invention, after a vector comprising two recognition sequences oriented in the opposite direction or one recognition sequence comprising a point-symmetric nucleotide sequence is introduced into a plant cell, the recombinase which recognizes the above-described recognition sequence functions is allowed to act during the growth of the cells.
For example, the following description is given for the case where a vector for introduction of a recognition sequence, which carries two recognition sequences oriented in the opposite direction, is introduced into a plant cell, and subsequently a vector for introduction of a recombinase gene, having a recombinase gene between by recognition sequences oriented in the same direction, is introduced into the plant cells to allow the recombinase to act transiently during the growth of the cells (
The recombinase gene, thus positioned in the vector for introduction of a recombinase gene and introduced into a plant cell, is incorporated and expressed in such a state it exists between the two recognition sequences oriented in the same direction even if incorporated into chromosomes of the plant cells; thus, after the recombinase is produced to some extent, the gene is disappeared and freed from the introduced chromosomes, and then disappears by the function of the recombinase produced by the gene itself. Thus, the recombinase functions transiently. With the vector of the third embodiment of the present invention, the transient function of a recombinase is ensured through such mechanisms and thus negative effects such as DNA instability due to constant expression of a recombinase gene in cells with target chromosomes disappeared can be prevented.
However, even a vector without a recognition sequence, having only this recombinase gene, can be used as a vector for introduction of a recombinase gene. As described above, the recombinase gene introduced into a plant cell can be expressed without being incorporated into chromosomes to allow transient function of a recombinase. Therefore, even a vector without a recognition sequence, having a recombinase gene, allows transient function of a recombinant enzyme in plant cells, into which the vector is introduced, by the functions of the free recombinase gene. When a recombinase is allowed to act transiently through such mechanism, the target chromosome is disappeared, and cells leaving no trace of the vector for introduction of the recombinase gene, as well as no trace of the vector for introduction of the recognition sequence (i.e., cells leaving no trace of genetic manipulation) can be obtained (
When a negative selectable marker gene is positioned in the vector used in the above-described first or second embodiment of the present invention or the vector for introduction of a recognition sequence, used in the third embodiment of the present invention) cells in which chromosomes are disappeared can be obtained more efficiently.
For examples when a vector comprising a negative selectable marker gene, outside of two recognition sequences oriented in the opposite direction together with a recombinase genes in the first embodiment of the present invention is introduced into a plant cell (
In the third embodiment of the present invention, the above-described negative selectable marker gene can be positioned together with a recombinase gene in the vector for introduction of a recombinase gene.
For example, when a vector comprising a recombinase gene without a recognition sequence is used as a vector for introduction of a recombinase genes and the recombinase gene positioned in this vector is introduced into a chromosome other than those to which the recognition sequence was introduced by the vector for introduction of a recognition sequence, the recombinase gene remains on the chromosome to which the gene was introduced, even after the target chromosome is disappeared and is expressed constantly to produce a recombinase with resultant negative effects such as DNA instability.
However, in this case, a vector comprising a negative selectable marker gene together with a recombinase gene is used as a vector for introduction of a recombinase gene, the negative selectable marker gene is also introduced to and remains on the chromosome even if a recombinase gene is introduced to and remains on the chromosome other than those to which the recognition sequence was introduced by a vector for introduction of a recognition sequence; thus, normal growth and differentiation are inhibited by culturing under conditions where the negative selectable marker gene functions. Said cells are thus disappeared, and cells to which the recombinase has been allowed to act transiently can reliably be obtained (
When a recombinase gene is positioned between two recognition sequences oriented in the same direction in a vector for introduction of a recombinase gene, cells in which the recombinase has been allowed to act transiently can be obtained more reliably by positioning a negative selectable marker gene between the two recognition sequences together with the recombinase gene.
When a vector for introduction of a recombinase gene in which a recombinase gene is positioned in such a state that it exists between two recognition sequences oriented in the same direction is introduced into a plant cell, the recombinase gene usually produces a recombinase to some extent even if incorporated into the chromosomes of plant cells, and is disappeared and freed from the introduced chromosomes and subsequently disappears (
However, also in this case, when a negative selectable marker gene is positioned in a vector for introduction of a recombinase gene as described above, this negative selectable marker gene behaves in the same manner as the recombinase gene for site-specific recombination; thus, the negative selectable marker gene also continues to exist on the chromosomes of cells when the recombinase gene continues to be expressed without being disappeared after introduction into the chromosomes of plant cells, and culturing under conditions where this negative selectable marker gene functions inhibits normal differentiation and growth of cells and eliminates the cells (
Hereinafter, the details of the present invention is described according to examples. However, the present invention is not limited to the examples described below. In the following examples, if not otherwise specified, further details of the experimental procedures followed Molecular Cloning (Sambrook et al. (1989)) or the manufacturer's instructions.
A plasmid, pCRScodN, having the NPTII structural gene linked with the promoter of the nopaline synthase gene (Nos-P) and the polyadenylation signal of the nopaline synthase gene (hereinafter, all polyadenylation signals are those derived from nopaline synthase) and codA structural gene linked with the 35S promoter (35S-P) and polyadenylation signal, oriented in the opposite direction, between recognition sequence RS derived from site-specific recombination system R/RS, was constructed. The codA structural gene was obtained by PCR method using genomic DNA of E. coli (DH5α, purchased from Toyobo Co., Ltd.) as a template and primer α represented by SEQ ID NO:1 (5′-gctctagagc atgtggaggc taacagtg-3′) and primer β represented by SEQ ID NO:2 (5′-gcgagctctc agtgctctac gtaggccg-3′).
The structure of pCRScodN is shown in
A plasmid, pTSsps, was constructed by inserting a DNA fragment obtained by annealing oligonucleotide, spsU, represented by SEQ ID NO:3 (5′-tgcagaataa ataaacgcca tggcacccgg gaaagaaata aaatgaaacg caaacacatg acctgcaggc acataagatg atacgcaagc gccgagctct actacgcaat ggeagacgca aaagcaggct acgcatgca) and oligonucleotide, spsL, represented by SEQ ID NO:4 (5′-tgcatggta gcctgctttt gcgtctgcca ttgcgtagta gagctcggcg cttgcgtatc atcttatgtg cctgcaggt atgtgtntgc gtttcatttt atttctttcc cgggtgccat ggcgtttatt tattctgoa-3′) into the restriction enzyme SmaI site of plasmid pTS1 (WO2004/87910) (
When this vector is introduced into a plant cell, the region between the right border (RB) and the left border (LB) derived from the T-DNA, indicated by the black triangles in the figure, is introduced into chromosomes. The codA gene is a gene encoding an enzyme which converts 5-fluorocytosine (5-FC) into cytotoxic 5-fluorouracil; thus, when plant cells to which cod gene is introduced into the chromosomes and expressed are cultured in a 5-FC supplemented medium, the cells are killed; thus, in this example, as described in the following II in detail, this gene is used as a negative selectable marker gene to selectively obtain cells in which chromosomes are disappeared. The NPTII gene functions as a selectable marker gene to select plant cells to which the above-described RB-LB region is introduced into chromosomes by this vector.
A plasmid, 128-35Rrubipt, having the ipt gene linked with the Rubisco promoter (Rub-P) and site-specific recombinase (R) structural gene linked with the 35S-P and polyadenylation signal, between RSs oriented in the same direction, was constructed (
A plasmid, pTSkss, was constructed by inserting a DNA fragment obtained by annealing oligonucleotide, kpnsseU, represented by SEQ ID NO:5 (5′-ctgcacgcta cctgcagg-3′) and oligonucleotide, kpnsseL, represented by SEQ ID NO:6 (5′-cctgcaggta gcgtgcag-3′) into the restriction enzyme SmaI site of plasmid pTS1 (WO2004/87910) (
Subsequently, the RSs and the region therebetween are excised from the 128-35Rrubipt with restriction enzyme SseI, was linked with the restriction enzyme SseI site of the above-described pTS35H to construct a vector plasmid, pTShygMRS35RRubipt, for the introduction of the recombinase gene [
When the vector constructed here for the introduction of the recombinase gene, pTShygMS35RRubipt, is introduced into a plant cell to which the above-described vector for introduction of the recognition sequence, pTSspsRScodN, was introduced, the R gene positioned in this pTShygMRS35RRubipt is expressed to produce the recombinase. In this case, when the cells are cultured and grown, the two chromosomes produced by duplication at the start of somatic cell division, having two RSs derived from pTSspsRScodN, oriented in the opposite direction, cause DNA recombination in the regions between the above-described two RSs by the function of the recombinase.
Among the cells in which such DNA recombination has been caused, a dicentric chromosome and acentric chromosome are produced in cells in which asymmetric recombination has been caused; as a result, daughter cells are produced, in which the structures derived from the above-described pTSspsRScodN (i.e., two RSs oriented in the opposite direction and chromosomes having the coda gene and others which exist in the region between these two RSs) are lost. However, in cells in which symmetric recombination has been caused, there is no substantial change in the chromosome after recombination. Thus, a chromosome with the structure derived from pTSspsRScodN is maintained. Therefore, when pTShygMRS35RRubipt is introduced into a plant cell to which pTSspsRScodN has been introduced and the cells are cultured in the presence of 5-FC, cells in which symmetric recombination has been caused are killed by the function of the codA gene which remains in the chromosome, and only cells in which chromosomes are disappeared by asymmetric recombination can be selected.
The R gene positioned in pTShygMRS35RRubipt, thus introduced into a plant cell, is incorporated and expressed in a state that it exists between the RSs oriented in the same direction even if incorporated into chromosomes of plant cells; thus, after a recombinase is produced to some extent, the gene is disappeared and freed together with the ipt gene from the chromosome, and then disappears by the function of the recombinase produced by the gene itself. Thus, the recombinase is allowed to act transiently (
When the R gene is not disappeared from chromosomes through the above-described mechanism in the pTShygMRS35RRubipt, the ipt gene functions as a negative selectable marker gene to eliminate relevant cells, and the Hpt gene functions as a selectable marker gene to select plant cells having chromosomes into which the above-described RB-LB region is introduced by this vector
A. tumefaciens 4404 strain was inoculated into 10 mL of a YEB liquid medium [5 g/L beef extract, 1 g/L yeast extract, 1 g/L peptone, 5 g/L sucrose, 2 mM MgSO4, pH 7.2 at 22° C. (hereinafter, pH at 22° C., unless otherwise specified)] and cultured at 28° C. until OD630 reaches 0.4-0.6. After harvesting of this culture medium by centrifugation at 6,900×g for 10 minutes at 4° C., the precipitated cells are suspended in 20 mL of 10 mM HEPES (pH 80) and the cells are collected again by centrifugation at 6,900×g for 10 minutes at 4° C., and the obtained cells are suspended into 200 μL of a YEB liquid medium to be used as cell solution for plasmid introduction.
Subsequently, 50 μL of this cell solution for plasmid introduction was mixed with 3 μL each of pTSspsRScodN and pTShygMRS35RRubipt which were prepared in I and II, respectively, in a 0.5 μL tube, and electroporation (Gene Pulser II System [BIORAD]) was conducted to introduce the above-described vector into A. tumefaciens 4404 strain. The cells after electroporation which 200 μL of the YEB liquid medium was supplemented, were cultured by shaking at 25° C. for 1 hour, and were seeded into a 50 mg/L kanamycin-supplemented YEB agar medium (agar 1.5 w/v %, other compositions are the same as those described above) and cultured at 28° C. for 2 days. As a result of this culture, cells which formed colonies were further introduced into the YEB liquid medium and cultured, and plasmids were extracted by the alkaline method, followed by digestion with restriction enzyme EcoRI or HindIII, and polyacrylamide gel electrophoresis was conducted to analyze the length of the restriction enzyme-digested products and demonstrated the introduction of pTSspsRScodN or pTShygMRS35RRubipt into A. tumefaciens 4404 strain. Cells into which the introduction of pTSspsRScodN was demonstrated were referred to as LBA4404 (pTSspsRScodN), and those into which the introduction of pTShygMRS35RRubipt was demonstrated as LBA4404 (pTShygMRS35RRubipt).
Nicotiana tabacum SR1 (hereinafter the same below unless otherwise specified) grown in an incubator, whose medial veins were removed from its leaves, was cut into about 8 mm square to obtain 36 leaf discs, which were immersed into an LBA4404 (pTSspsRScodN) culture solution (OD630=0.25, after overnight culture in YEB liquid medium, culture concentration was adjusted by dilution with sterilized water) for about 1 minute for infection, and after removal of an excess culture solution on a sterile filter, were put on a 50 mg/L acetosyringone-supplemented MS agar medium without a plant hormone (hormone free) (T. Murashige and F. Skoog Physiol. Plant. 15: 473 (1962); however, agar was supplemented at 0.8 w/v %) on upper sides of the leaves and cultured for 3 days at 25° C. under full light (explant, plant tissue and plant individual were cultured under these conditions unless otherwise specified).
The above-described cultured leaf discs were introduced into MS agar medium supplemented with 6-benzylaminopurine (1 mg/L), naphthalene acetic acid (0.1 mg/L), carbenicillin (500 mg/L) and kanamycin (200 mg/L), and after the culture was continued, 24 adventitious buds were redifferentiated, and these adventitious buds separated were introduced to and further cultured on a hormone-free MS agar medium supplemented with carbenicillin (500 mg/L) and kanamycin (200 mg/L) for rooting, and 12 rooting individuals were obtained from 12 adventitious buds, and finally 12 lineages of kanamycin-resistant recombinants each derived from these 12 rooting individuals could be obtained.
Seeds were collected from acclimated rooting individuals for the obtained 12 lineages of kanamycin-resistant recombinants and seeded into a hormone free MS agar medium containing kanamycin (200 mg/L) and one kanamycin-resistant seedling strain, budded and grown was each selected for one lineage.
Chromosomal DNA was extracted from the 12 strains of 12 kanamycin-resistant recombinant lineages, obtained in IV, by CTAB method, and was digested with restriction enzyme HindIII to be used for 0.8% agarose gel electrophoresis. The electrophoretic surface of the electrophoresed agarose gel after alkaline and acid treatment was transcribed to a nylon membrane and was hybridized with a probe with a sequence homologous to codA gene preliminarily labeled by DIG PCR labeling kit (purchased from Boehringer Mannheim). After hybridization, chemiluminescence detection was conducted with DIG Wash and Block Buffer (purchased from Boehringer Mannheim), and introduction of a copy of pTSspsRScodN was demonstrated in one lineage (Cod N-23) of the above-described 12 lineages.
In V, LBA4404 (pTShygMS35RRubipt) was infected to recognition sequence-introduced Nicotiana tabacum Cod N-23, in which introduction of a copy of pTSspsRScodN was demonstrated, in the same manner as in IV. After infection, 64 leaf discs co-cultured with LBA4404 (pTShygMRS35RRubipt) for 3 days were introduced to an MS agar medium containing naphthalenacetic acid (1 mg/L), benzoyladenine (0.1 mg/L), carbenicillin (500 mg/L) and hygromycin (20 ml) and the culture was continued to obtain 90 calluses, and these 90 calluses were introduced to mediums of the same compositions, followed by continuing the culture for 4 weeks, and 50 adventitious buds were obtained. When these adventitious buds were subcultured on a hormone-free MS agar medium, 24 rooting individuals could be obtained.
Chromosomal DNA was extracted from 24 rooting individuals obtained in VI with Fast DNA Kit (BIO 101 Inc.), and PCR analysis was conducted using primer Km1 represented by SEQ ID NO:7 (5′-agaggctatt cggctatgca-3′) and primer Km2 represented by SEQ ID NO:8 (5′-ccatgatatt cggcaagcag-3′) which bind to the NPTII structural gene, primer RBS1 represented by SEQ ID NO:9 (5′-actgatagtt taaactgaag gcggg-3′) which binds to the proximity of the right border of pTSspsRScodN and primer SPR 1a represented by SEQ ID NO:10 (5′-atgcgttta tttattctgc-3′) which binds to the sequence derived from spsU of pTSspsRScodN, primer SPL 1a represented by SEQ ID NO:11 (5′-acataagatg atacgcaagc-3′) which binds to the sequence derived from spsL of pTSspsRScodN and primer pBSPh02 represented by SEQ ID NO:12 (5′-aagccggcga acgtggcgag aa-3′) which binds to the proximity of the left border of pTSspsRScodN and primer Hm1 represented by SEQ ID NO:13 (51-cgtctgtcga gaagtttctg-3′) and primer Hm2 represented by SEQ ID NO:14 (5′-ctatcggcga gtacttctac-3′) which bind to the Hpt gene.
PCR reaction was conducted with 1 μg of DNA, dissolved in the mixture of 0.2 μM each of the primers, 10 mM Tris-HCl (pH 8.8 at 25° C.), 50 mM KCl, 1.5 mM MgCl2, 1 w/v % Triton X-100, 0.1 mM dNTPs, 1.25 units of Taq polymerase (purchased from CETUS) and 50 μL of the PCR buffer solution (after heating at 94° C. for 1.5 minutes) 30 cycles of 94° C. for 30 seconds, 60° C. for 30 seconds and 72° C. for 2 minutes). The PCR reaction solution was used for agarose gel electrophoresis to detect amplified DNA fragments.
Here, when the Nicotiana tabacum used in the PCR analysis has chromosomes in which the structure derived from pTSspsRScodN is retained, DNA fragments of approximately 500 bp (Km1-Km2), approximately 200 bp (RBS1-SPR1a) and approximately 100 bp (SPL1a-pBSPh02) will be amplified (
As a result of the PCR analysis, amplified DNA fragments of approximately 900 bp were detected for all the 24 individuals used for electrophoresis. Amplified DNA fragments of approximately 500 bp, 200 bp and 100 bp were detected in 20 individuals, while none of these 3 DNA fragments was amplified in 4 individuals (Nos. 30, 34, 42 and 53). Thus, these 4 individuals were selected as those with predetermined chromosomes were disappeared (hereinafter, simply referred to as chromosome-disappeared individuals), and subsequently the following experiment was conducted.
In
The leaves of about 5 mm square were collected from the chromosome-disappeared individuals selected in A (Nos. 30, 34, 42 and 53) and immersed into solution A of the DNA reagent kit for plant analysis (Partec 06-5-4004), and after being immersed in this solution and shredded with a razors 50 μL of this was filtered through a CellTrics filter (Pante 06-4-2371), and the filtrate was collected. Using this filtrate to which 300 μL of solution B of the above-described reagent kit (Partec 065-4004) was added as a sample, flow cytometry analysis of chromosomal DNA amount was conducted using a ploidy Analyzer PA type (Partec). Here, the chromosomal DNA amount is detected as fluorescence intensity (FLI); the larger the chromosomal DNA amount is, the stronger the fluorescence intensity is indicated.
The results of the flow cytometry analysis are shown in Table 1.
As can be seen in Table 1, the DNA amounts of all the individuals, selected as chromosome-disappeared individuals in A (Nos. 30, 34, 42 and 53), are smaller than that of the wild type, suggesting that these are chromosome-disappeared individuals.
Specifically, in this example, chromosome-disappeared individuals can be easily produced with a probability of 4 individuals/64 leaf discs (=6.3×10−2) from plant individuals to which a vector for introduction of a recombinase gene was introduced; in addition, the production was easy, which could be conducted without proceeding through germ cells and required only use of a vector with a very simple structure, very common gene transfer technique and plant tissue culturing technique.
The RSs and the region therebetween are excised from the 128-35Rrubipt, constructed in Example 1-II, with restriction enzyme SseI, was linked with the restriction enzyme SseI site of the pTL7 (H. Ebinuma et al., Molecular Method of Plant Analysis, 22: 95 (2002)) to construct a vector plasmid, pTL7MRS35RRubipt, for the introduction of recombinase gene [
When this vector for introduction of recombinase gene, pTL7MRS35RRubipt, is introduced into a plant cell to which the above-described vector for introduction of recognition sequence, pTSspsRScodN, was introduced, and the cells are cultured and grown, the two chromosomes produced by duplication, having two RSs derived from pTSspsRScodN, oriented in the opposite direction, cause DNA recombination in the same manner as in Example 1; in the case of asymmetric recombination, daughter cells are produced in which the structures derived from the above-described pTSspsRScodN (i.e., two RSs oriented in the opposite direction and chromosomes having the codA gene and others which exist in the region between these two RSs) are lost, and in the case of symmetric recombination, a chromosome with these structures is maintained. Therefore, when pTL7MRS35RRubipt is introduced into a plant cell to which pTSspsRScodN has been introduced and the cells are cultured in the presence of 5-FC, cells in which symmetric recombination has been caused are killed by the function of the codA gene which remains in the chromosomes, and only cells in which chromosomes are disappeared by asymmetric recombination can be selected.
The R gene and ipt gene positioned in pTL7MRS35RRubipt for the introduction of the recombinase gene functions in the same manner as in Example 1. Specifically, when the R gene is incorporated into the chromosomes of plant cells, after a recombinase is produced to some extent, the R gene is disappeared and freed together with the ipt gene from the chromosomes to which they are introduced by the function of the recombinase produced by the gene itself, and then disappears. When the R gene is not disappeared from chromosomes through the above-described mechanism, the ipt gene functions as a negative selectable marker gene to eliminate relevant cells.
The pTL7MRS35RRubipt for the introduction of a recombinase gene, constructed in the above I, was introduced into A. tumefaciens 4404 strain in the same manner as in Example 1-III, and after DNA analysis to demonstrate this, cells were referred to as LBA4404 (pT7MRS35RRubipt)
The LBA4404 (pTL7MRS35RRubipt), obtained in the above-described II, was infected to the recognition sequence-introduced Nicotiana tabacum Cod N-23, in which introduction of a copy of pTSspsRScodN was demonstrated in Example 1-V, to introduce a vector for introduction of a recombinase gene (pTL7MRS35RRubipt) into recognition sequence-introduced Nicotiana tabacum. The infection was conducted in the same manner as in Example 1-IV.
After infection, 32 leaf discs co-cultured with LBA4404 (pTL7MRS35RRubipt) for 3 days were introduced to an MS agar medium containing 6-benzylaminopurine (1 mg/L), naphthalenacetic acid (0.1 mm) and carbenicillin (500 mg/L) and cultured for 1 week, and subsequently were introduced to the MS agar medium containing 6-benzylaminopurine (1 mg/L), naphthalenacetic acid (0.1 mg/L), carbenicillin (500 mL) and 5-FC (0.2 mg/L), and the culture was continued to obtain 24 calluses, and these 24 calluses were introduced to mediums of the same compositions, followed by continuing the culture, and 16 adventitious buds derived from 16 calluses were obtained. When these adventitious buds were subcultured on a hormone-free MS agar medium, 6 rooting individuals could be obtained.
Chromosomal DNA was extracted from 6 rooting individuals obtained in III with Fast DNA Kit (BIO 101 Inc.), and PCR analysis was conducted using primers Km1 and Km2, primers RBS1 and SPR1a, primers SPL1a and pBSPh02, primer RBS2 represented by SEQ ID NO:15 (5′-aaacgacaat ctgatcatga gcgga-3′) which binds to the T-DNA of the right border of pTL7MRS35RRubipt and primer Lza9 represented by SEQ ID NO:16 (5′-ggctcgtatg ttgtgtggaa ttgt-3#), primer Ra represented by SEQ ID NO:17 (5′-coaaggatac tgaaatttca acaat-3′) which binds to the R gene of pTL7MRS35RRubipt and primer Rc represented by SEQ ID NO:18 (5′-ttatttgaaa gatatgaagc tgtca-3′), and primer OMT1 represented by SEQ ID NO:19 (5′-taagacctat atccactca aaaca-3′) and primer OMT3 represented by SEQ ID NO:20 (5′-agctagccct gtggcgtgcc ttcca-3′) which bind to the O-methyltransferase (OMT) gene of the genome of Nicotiana tabacum, and PCR analysis was conducted under the same conditions as those in Example 1.
Here, when the Nicotiana tabacum used in the PCR analysis has chromosomes in which the structure derived from pTSspsRScodN is retained, DNA fragments of approximately 500 bp (Km1-Km2), approximately 200 bp (RBS1-SPR1a) and approximately 100 bp (SPL1a-pBSPh02) will be amplified (
When this chromosome disappearance occurs without incorporation of pTL7MRS35RRubipt into chromosomes, a DNA fragment of approximately 800 bp (OMT1-OMT3) alone will be amplified (
As a result of the PCR analysis, an amplified DNA fragment of approximately 800 bp was detected for all 6 individuals used for electrophoresis, while none of the amplified DNA fragments of approximately 500 bp, 200 bp, 100 bp and 1.0 kbp were detected. The amplified DNA fragment of approximately 400 bp was detected in 4 of the 6 individuals (Nos. 1, 2, 4 and 7), but was not detected for the other 2 individuals (Nos. 8 and 12).
The above results suggest that all these 6 individuals are chromosome-disappeared individuals, of which two individuals (Nos. 8 and 12) are individuals in which chromosome disappearance occurred without pTL7MRS35RRubipt being incorporated, i.e., individuals derived from cells in which, when pTL7MRS35RRubipt was introduced in the above-described III, the R gene positioned in it was not incorporated into chromosomes but remained in a free state to be expressed, and as a result, chromosome disappearance occurred; other four individuals (Nos. 1, 2, 4 and 7) are individuals in which chromosome disappearance occurred without pTL7MRS35RRubipt being incorporated, i.e. individuals derived from cells in which when pTL7MRS35RRubipt was introduced in the above-described III, the R gene positioned in it was also incorporated into chromosomes, and as a result, chromosome disappearance occurred. In all four individuals in which incorporation of pTL7MRS35RRubipt into chromosomes caused chromosome disappearances after incorporation of this pTL7MRS35RRubipt, the structure derived from pTL7MRS35RRubipt, such as the R gene, was considered to be disappeared by the function of the recombinase produced by R gene expression.
In
Flow cytometry analysis was conducted on the above-described 6 individuals (Nos. 1, 2, 4, 7, 8 and 12), determined as chromosome-disappeared individuals in A, in the same manner as in VI-B of Example 1.
The results of the flow cytometry analysis are shown in Table 2.
As can be seen in Table 2, the DNA amounts of all the six individuals, demonstrated as chromosome-disappeared individuals in A (Nos. 1, 2, 4, 7, 8 and 12), are smaller than that of the wild type, suggesting that these are chromosome-disappeared individuals.
Specifically, in this example, chromosome-disappeared individuals could be produced with a probability of 6 individuals/32 leaf discs (=1.9×10−1), from plant individuals to which a vector for introduction of a recombinase gene was introduced; furthermore, in the introduction of a vector for introduction of a recombinase, only chromosome-disappeared individuals could be obtained as rooting individuals by culturing tissues after the introduction in the presence of 5-FC. Two of the six (33%) produced chromosome-disappeared individuals, are individuals produced without a recombinase gene being incorporated, and had no trace of the vector for introduction of a recombinase gene, as well as no trace of the vector for introduction of a recognition sequence, left in the cells (i.e., individuals without trace of genetic manipulation being left).
The production was easy, which could be conducted without proceeding through germ cells and required only use of a vector with very simple structure, very common gene transfer technique and plant tissue culturing technique.
A plasmid vector for introduction of recombinase gene, pTL735R, was constructed by linking the R structural gene linked with 35S-P and the polyadenylation signal to the EcoRI site of pTL7 (
When the vector for introduction of a recombinase gene, pTL735R, is introduced into a plant cell to which the above-described vector for introduction of a recognition sequences pTSspsRScodN, was introduced, and the cells are cultured and grown, DNA recombination occurs between the two chromosomes, having two RSs derived from pTSspsRScodN, oriented in the opposite direction; in the case of asymmetric recombination, daughter cells are produced in which the structures derived from this pTSspsRScodN (i.e., two RSs oriented in the opposite direction and chromosomes having the codA gene and others which exist in the region between these two RSs) are lost, and in the case of symmetric recombination, a chromosome with these structures is maintained. Therefore, when pTL735R is introduced into a plant cell to which pTSspsRScodN has been introduced and the cells are cultured in the presence of 5-FC, cells in which symmetric recombination has been caused are killed by the function of the codA gene which remains in the chromosomes, and only cells in which chromosomes are disappeared by asymmetric recombination can be selected.
The R gene positioned in pTL735R for the introduction of a recombinase gene, introduced into a plant cell is expressed regardless of whether being incorporated into the chromosomes of the cells; however, when the R gene is expressed without being incorporated into chromosomes, the recombinase functions transiently, and the chromosomes are disappeared by the above-described mechanism, furthermore, cells with no trace of the vector for introduction of recombinase genes pTL735R, as well as no trace of the vector for introduction of recombinase, pTSspsRScodN, left in the cells, can be obtained; thus, in this example, the function of the free R gene is utilized.
The vector for introduction of recombinase genes pTL735R, constructed in the above I, was introduced into A. tumefaciens 4404 strain in the same manner as in Example 1-III, and after DNA analysis to demonstrate this, these cells were referred to as LBA4404 (pTL735R),
The LBA4404 (pTL73 SR), obtained in the above-described II, was infected to the recognition sequence-introduced Nicotiana tabacum Cod N-23, in which introduction of a copy of pTSspsRScodN was demonstrated, to introduce a vector for introduction of a recombinase gene (pTL735R) into the recognition sequence-introduced Nicotiana tabacum. The infection was conducted in the same manner as in Example 1-IV.
After infection, 32 leaf discs co-cultured with LBA4404 (pTL735R) for 3 days were introduced to an MS agar medium containing 6-benzylaminopurine (1 mg/L), naphthalenacetic acid (0.1 mg/L) and carbenicillin (500 mg/L) and cultured for 1 week and subsequently were introduced to an MS agar medium containing 6-benzylaminopurine (1 mg/L), naphthalenacetic acid (0.1 mg/L), carbenicillin (500 mg/L) and 5-FC (0.2 mg/L), and culture was continued to obtain 19 calluses, and these 19 calluses were introduced to mediums of the same compositions, followed by continuing the culture, and 14 adventitious buds derived from 14 calluses were obtained. When these adventitious buds were subcultured on a hormone-free MS agar medium, 14 rooting individuals could be obtained.
Chromosomal DNA was extracted from the 14 rooting individuals, obtained in III, with a Fast DNA Kit (BIO 101 Inc.), and PCR analysis was conducted using primers Km1 and Km2, primers RBS1 and SPR1a, primers SPL1a and pBSPh02, used in Examples 1 and 2, and primers Ra and Rc and primers OMT1 and OMT3, used in Example 2, and PCR analysis was conducted under the same conditions as those in Example 1.
Here, when the Nicotiana tabacum used in the PCR analysis has chromosomes in which the structure derived from pTSspsRScodN is retained, DNA fragments of approximately 500 bp (Km1-Km2), approximately 200 bp (RBS1-SPR1a) and approximately 100 bp (SPL1a-pBSPh02) will be amplified (
When this chromosome disappearance occurs without incorporation of pTL736R into chromosomes, a DNA fragment of approximately 800 bp (OMT1-OMT3) alone will be amplified (
As a result of the PCR analysis, an amplified DNA fragment of approximately 800 bp was detected for all 14 individuals (R-1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13 and 15) used for electrophoresis. In 11 individuals (R-1, 2, 3, 4, 5, 6, 7, 9, 10, 11 and 15) of these, none of the amplified DNA fragments of approximately 500 bp, 200 bp and 100 bp were detected, in addition, the amplified DNA fragment of approximately 1.0 kb was detected in 6 individuals (R-3, 5, 7, 9, 11 and 15), but was not detected in 5 individuals (R-1, 2, 4, 6 and 10).
Thus, in this example, 11 chromosome-disappeared individuals were obtained, of which 5 individuals (R-1, 2, 4, 6 and 10) are considered to be individuals in which chromosome disappearance occurred without pTL735R being incorporated, i.e., individuals derived from cells in which, when pTL735R was introduced in the above-described III, the R gene positioned in it was not incorporated into chromosomes but remained in a free state to be expressed, and as a result, chromosome disappearance occurred.
In
Flow cytometry analysis was conducted on the above-described 5 individuals (R-1, 2, 4, 6 and 10) of the 11 individuals, determined as chromosome-disappeared individuals in A, in the same manner as in VI-B of Example 1.
The results are shown in Table 3.
As can be seen in Table 3, the DNA amounts of all five individuals (R-1, 2, 4, 6 and 10), are smaller than that of the wild type, suggesting these are chromosome-disappeared individuals.
Specifically, in this example, chromosome-disappeared individuals could be produced without incorporation of a recombinase gene into the chromosomes with a probability of 5 individuals/32 leaf discs (=1.6×10−1), from plant individuals to which a vector for introduction of a recombinase gene was introduced; chromosome-disappeared individuals could be obtained with no trace of the vector for introduction of a recombinase gene, as well as no trace of the vector for introduction of a recognition sequence, left in the cells (i.e., individuals without trace of genetic manipulation being left).
The production was easy, which could be conducted without proceeding through germ cells and required only use of a vector with a very simple structure, very common gene transfer technique and plant tissue culturing technique.
A plasmid vector for introduction of recombinase gene, pTL7rubipt35R, was constructed by linking the ipt gene linked with Rub-P to the KpnI site of pTL735R (
When this vector for introduction of recombinase gene, pTL7rubipt35R, is introduced into a plant cell to which the above-described vector for introduction of recognition sequence, pTSspsRScodN, was introduced, and the cells are cultured and grown, DNA recombination occurs between the two chromosomes, produced by duplication, having two RSs derived from pTSspsRScodN, oriented in the opposite direction, in the same manner as in Examples 1, 2 and 3; in the case of asymmetric recombination, daughter cells are produced, in which the structures derived from this pTSspsRScodN (i.e., chromosome having two RSs oriented in the opposite direction and the codA gene and others which exist in the region between these two RSs) are lost and in the case of symmetric recombination, a chromosome with these structures is maintained. Therefore, when pTL7rubipt35R is introduced into a plant cell to which pTSspsRScodN has been introduced and the cells are cultured in the presence of 5-FC, cells in which symmetric recombination has been caused are killed by the function of the codA gene which remains in the chromosomes, and only cells in which chromosomes are disappeared by asymmetric recombination can be selected.
The R gene positioned in the vector for introduction of recombinase gene, pTL7rubipt35R introduced into a plant cell, is expressed regardless of whether being incorporated into the chromosomes of the cells, in the sane manner as for the R gene positioned in the vector for introduction of recombinase gene, pTL735R constructed in Example 3; when the R gene is expressed without being incorporated into chromosomes, the recombinase functions transiently, and the chromosomes is disappeared by the above-described mechanism, furthermore, cells with no trace of the vector for introduction of the recombinase gene (pTL7rubipt35R), as well as no trace of the vector for introduction of the recognition sequence (pTSspsRScodN), left in the cells, can be obtained.
However, the ipt gene is also positioned in the vector for introduction of the recombinase gene (pTL7rubipt35R), constructed in this example, as a negative selectable marker gene together with the R gene and thus introduction of pTL7rubipt35R into a plant cell inhibits normal growth and differentiation of cells having this chromosome since the apt gene is also incorporated into this chromosome and expressed even if the R gene positioned in this vector is incorporated into the chromosomes of the cells. The cells are thus disappeared, and cells in which the recombinase has been allowed to act transiently can be reliably obtained. II. Introduction of a Vector for Introduction of Recombinase Gene (pTL7rubipt35R) into Agrobacterium
The pTL7rubipt35R for the introduction of the recombinase gene, constructed in the above I, was introduced into A. tumefaciens 4404 strain in the same manner as in Example 1-III, and after DNA analysis to demonstrate this, the strain was referred to as LBA4404 (pTL7rubipt35R). III. Introduction of a Vector for Introduction of Recombinase Gene (pTL7rubipt35R) into Recognition Sequence-Introduced Nicotiana tabacum
The LBA4404 (pTL7rubipt35R), obtained in the above-described II, was infected to the recognition sequence-introduced Nicotiana tabacum Cod N-23, in which introduction of a copy of pTSspsRScodN was demonstrated in Example 1-V, to introduce a vector for introduction of the recombinase gene (pTL7rubipt35R) into the recognition sequence-introduced Nicotiana tabacum. The infection was conducted in the same manner as in Example 1-IV.
After infection, 32 leaf discs co-cultured with LBA4404 (pTL7rubipt35R) for 3 days were introduced to an MS agar medium containing 6-benzylaminopurine (1 mg/L), naphthalenacetic acid (0.1 mg/L) and carbenicillin (500 mg/L) and cultured for 1 week and subsequently were introduced to an MS agar medium containing 6-benzylaminopurine (1 mg/L), naphthalenacetic acid (0.1 mg/L), carbenicillin (500 mg/L) and 5-FC (0.2 mg/L), and the culture was continued to obtain 53 calluses, and these 53 calluses were introduced to mediums of the same compositions, followed by continuing the culture, and 5 adventitious buds derived from 5 calluses were obtained. When these adventitious buds were subcultured on a hormone-free MS agar medium, 5 rooting individuals could be obtained.
Chromosomal DNA was extracted from the 5 rooting individuals, obtained in III, in the same manner as Example 39 with a Fast DNA Kit (BIO 101 Inc.) and PCR analysis was conducted using primers Km1 and Km2, primers RBL1 and SPR1a, and primers SPL1a and pBSPh02, used in Examples 1 and 2, and primers Ra and Rc and primers OMT1 and OMT3, used in Example 2, and PCR analysis was conducted under the same conditions as those in Example 1.
Therefore, when the Nicotiana tabacum used in the PCR analysis has chromosomes in which the structure derived from pTSspsRScodN is retained, DNA fragments of approximately 500 bp (Km1-Km2), approximately 200 bp (RBS1-SPR1a) and approximately 100 bp (SPL1a-pBSPh02) will be amplified (
When this chromosome disappearance occurs without incorporation of pTL7rubipt35R into chromosomes, a DNA fragment of approximately 800 bp (OMT1-OMT3) alone will be amplified (
As a result of the PCR analysis, an amplified DNA fragment of approximately 800 bp was detected for all 5 individuals (I-2, 4, 8, 10 and 11) used for electrophoresis, while amplified DNA fragments of approximately 500 bp, 200 bp, 100 bp and 1.0 kb were not detected.
Thus, in this example, 5 chromosome-disappeared individuals were obtained (I-2, 4, 8, 10 and 11), all of which are considered to be individuals in which chromosome disappearance occurred without pTL7rubipt35R being incorporated, i.e., individuals derived from cells in which, when pTL7rubipt35R was introduced in the above-described III, the R gene positioned in it was not incorporated into chromosomes but remained in a free state to be expressed, and as a result, chromosome disappearance occurred.
In
Flow cytometry analysis was conducted on the above-described 5 individuals (I-2, 4, 8, 10 and 11), determined as chromosome-disappeared individuals in A, in the same manner as in VI-B of Example 1.
The results are shown in Table 3.
As can be seen in Table 3, the DNA amounts of all the above-described 5 individuals (I-2, 4, 8, 10 and 11) are smaller than that of the wild type, suggesting these are chromosome-disappeared individuals.
Specifically, in this example, chromosome-disappeared individuals could be obtained with a probability of 5 individuals/32 leaf discs (=1.6×10−1), from plant individuals to which a vector for introduction of a recombinase gene was introduced. Furthermore, in this example, a negative selectable marker gene (ipt gene) positioned in the vector together with a recombinase gene inhibited the dedifferentiation of cells, with a recombinase gene incorporated into the chromosomes, into rooting individuals and thus, in all the obtained chromosome-disappeared individuals, the chromosomes were disappeared without the recombinase gene being incorporated into the chromosomes, i.e., individuals with no trace of the vector for introduction of the recombinase gene, as well as no trace of the vector for introduction of the recognition sequence, left in the cells (i.e., individuals without trace of genetic manipulation being left).
The production was easy, which could be conducted without proceeding through germ cells and required only use of a vector with a very simple structure, very common gene transfer technique and plant tissue culturing technique.
While the invention has been described in detail and with reference to specific embodiments thereof, it will be apparent to one skill in the art that various changes and modifications can be made therein without departing from the spirit and scope thereof.
This application is based on Japanese patent application No. 2004-382394 filed on Dec. 8, 2004 and Japanese patent application No. 2005-174225 filed on May 18, 2005, the entire contents of which are incorporated hereinto by reference, All references cited herein are incorporated in their entirety.
The present invention provides a simple aneuploid production process, applicable to all species, without producing unexpected damage to chromosomes other than a chromosome which is to be disappeared.
SEQ ID NO:1—Description of artificial sequence: Synthetic DNA
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SEQ ID NO:20—Description of artificial sequence: Synthetic DNA
| Number | Date | Country | Kind |
|---|---|---|---|
| 2004-382394 | Dec 2004 | JP | national |
| 2005-174225 | May 2005 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP05/23184 | 12/8/2005 | WO | 00 | 2/13/2008 |
