eISSN: 2221-6197 DOI: 10.31301/2221-6197

Modern concepts about relationships in the wheat-aegilops alliance

Year: 2016

Pages: 297-310

Number: Volume 8, issue 4

Type: scientific article

Summary:

In the early twentieth century then-known species of wheat only on the basis of morphological differences were divided into three groups: Einkorn, Emmer and Spelta. Later, this division was confirmed, as it became clear that these groups differ in their level of ploidy. So, einkorn is diploid, emmer is tetraploid, and spelta - hexaploid with chromosome numbers of 14 (2n=2x), 28 (2n=4x) and 42 (2n=6x), respectively. It turned out that polyploid species are allopolyploids, and their formation involved the types of the genera Triticum and Aegilops submitted, at least 12 individual diploid genomes, but in the evolution of polyploid wheat Nature for their creation was used no more than 6 genomes and only 3 of them that form the hexaploid bread and tetraploid macaroni wheat, is currently "feed" humanity. And what types of wheat and aegilops become donors of these subgenomes are not clear. The importance of determining the true donors of wheat subgenomes is that this knowledge will give a new stimulus to more conscious experiments to create new polyploid wheat with improved economic-useful features, because in order to purposefully try to create a new polyploid form with the best properties, it is imperative to know what actually the genomes of diploid species of wheat-aegilops alliance unites by Nature in tetraploid and hexaploid wheat in both turgidum-aestivum and timopheevii series. Modern methods of molecular biology, technologies including whole genome sequencing of the new generations, enable a new level to explore the relationship of genomes and subgenomes of wheat and aegilops that allows to speculate on the donation of subgenomes with more confidence. Determination of the nucleotide sequences of the complete genomes of T.aestivum, T.uratu and Ae.tauschii, as well as plastomes of several species of wheat and aegilops and chondriome of bread wheat is an extremely important milestones in the study of wheat-aegilops alliance and shed new light on the phylogenetic relationships of these cereals. The cited literature covers more than three hundred years period.

Keywords:

wheat, aegilops, genone, subgenome, DNA, sequencing, NGS, donor, evolution, phylogeny, Triticum, Aegilops

References:

  1. Вавилов Н.И. К познанию мягких пшениц (систематико-географический этюд) // Труды по прикладной ботанике и селекции. 1922-1923. Т.13. С.149-205.
  2. Вахитов В.А., Чемерис А.В., Сабиржанов Б.Е., Ахунов Э.Д., Куликов А.М., Никоноров Ю.М., Гималов Ф.Р., Бикбулатова С.М., Баймиев Ал.Х. Филогенетические взаимоотношения родов Triticum L. и Aegilops L. нуклеотидные последовательности промоторных областей рДНК их отдельных представителей // Генетика. 2003. Т.39, №1. С.5-17.
  3. Дорофеев В.Ф., Коровина О.Н. // Культурная флора СССР. 1979. Т.1. Пшеница. Ленинград: Колос, Ленинградское отделение. 348 с.
  4. Дорофеев В.Ф., Мигушова Э.Ф. Новое в эволюции и систематике пшеницы // Докл. ВАСХНИЛ. 1981. №2. С.6-9.
  5. Дорофеев В.Ф., Удачин Р.А., Семенова Л.В. и др. Пшеницы мира // Л., Колос. 1987. 560 С.
  6. Гончаров Н.П. Сравнительная генетика пшениц и их сородичей / Новосибирск: Сиб. унив. изд-во, 2002. 252 с.
  7. Гончаров Н.П. Константин Андреевич Фляксбергер // Историко-биологические исследования. 2013. Т.5. С.106-108.
  8. Жангазиев А.С. Генетические основы систематики пшениц в роде Triticum L. // Вестник КазНУ. Серия биологическая. 2011. №4. С.64-70.
  9. Мартынов И.И. Три ботаника, или Сокращение систем Турнефорта, Линнея и Жюсьё, С кратким описанием жизни каждого, показанием прочих Систематиков и Ботаников, и начертанием Ботаники, каковую желательно бы иметь, выбранное из иностранных писателей / СПб.: Типография Департамента народного просвещения. 1821. 239 с.
  10. Митрофанова О.Д., Удачин Р.А. Константин Андреевич Фляксбергер – основоположник научного изучения пшеницы в России // Вестник ВОГиС. 2007. Т.11. 591-608.
  11. Рожевиц Р.Ю., Шишкин Б.К. Флора СССР. Т.2. Л. 1934. 778 С.
  12. Фляксбергер К.А. О вхождении пшеницы в культуру // Природа. 1929. №11. С. 965-971.
  13. Фляксбергер К.А. Пшеницы. М.-Л. ОГИЗ. 1935. 261 С.
  14. Фляксбергер К.А. Хлебные злаки. Пшеница. / Культурная флора СССР. Т.1. М.-Л. Сельхозгиз. 1935а. С.19-434.
  15. Цвелев Н.Н. Злаки СССР // Л., Наука. 1976. 788 с.
  16. Adonina I.G., Goncharov N.P., Badaeva E.D., Sergeeva E.M., Petrash V., Salina E.A. (GAA)n microsatellite as an indicator of the A genome reorganization during wheat evolution and domestication // Comp. Cytogenet. 2015. V.9. P.533-547. doi: 10.3897/CompCytogen.v9i4.5120.
  17. Badaeva E.D., Amosova A.V., Goncharov N.P., Macas J., Ruban A.S., Grechishnikova I.V., Zoshchuk S.A., Houben A. A Set of Cytogenetic Markers Allows the Precise Identification of All A-Genome Chromosomes in Diploid and Polyploid Wheat // Cytogenet. Genome Res. 2015;146(1):71-9. doi: 10.1159/000433458.
  18. Bahieldin A., Al-Kordy M.A., Shokry A.M., Gadalla N.O., Al-Hejin A.M., Sabir J.S., Hassan S.M., Al-Ahmadi A.A., Schwarz E.N., Eissa H.F., El-Domyati F.M., Jansen R.K. Corrected sequence of the wheat plastid genome // C. R. Biol. 2014. V.337. P.499-502. doi: 10.1016/j.crvi.2014.07.001.
  19. Berkman P.J., Lai K., Lorenc M.T., Edwards D. Next-generation sequencing applications for wheat crop improvement // Am. J. Bot. 2012. V.99. P.365-371. doi: 10.3732/ajb.1100309.
  20. Bernardo A., Wang S., St. Amand P., Bai G. Using Next Generation Sequencing for Multiplexed Trait-Linked Markers in Wheat // PLoS One. 2015 Dec 1;10(12):e0143890. doi: 10.1371/journal.pone.0143890.
  21. Brenchley R., Spannagl M., Pfeifer M., Barker G.L., D'Amore R., Allen A.M., McKenzie N., Kramer M., Kerhornou A., Bolser D., Kay S., Waite D., Trick M., Bancroft I., Gu Y., Huo N., Luo M.C., Sehgal S., Gill B., Kianian S., Anderson O., Kersey P., Dvorak J., McCombie W.R., Hall A., Mayer K.F., Edwards K.J., Bevan M.W., Hall N. Analysis of the bread wheat genome using whole-genome shotgun sequencing // Nature. 2012. V.491. P.705-710. doi: 10.1038/nature11650.
  22. Briggle L.W., Reitz L.P. Classification of Triticum species and of wheat varieties grown in the United States / USDA. Technical Bulletin No. 1278. 1963.
  23. Cui P., Liu H., Lin Q., Ding F., Zhuo G., Hu S., Liu D., Yang W., Zhan K., Zhang A., Yu J. A complete mitochondrial genome of wheat (Triticum aestivum cv. Chinese Yumai), and fast evolving mitochondrial genes in higher plants // J. Genet. 2009. V.88. P.299-307.
  24. Demir P., Onde S., Severcan F. Phylogeny of cultivated and wild wheat species using ATR-FTIR spectroscopy // Spectrochim. Acta A Mol. Biomol. Spectrosc. 2015. V.135. P.757-763. doi: 10.1016/j.saa.2014.07.025.
  25. Deng P., Wang M., Feng K., Cui L., Tong W., Song W., Nie X. Genome-wide characterization of microsatellites in Triticeae species: abundance, distribution and evolution // Sci. Rep. 2016 Aug 26;6:32224. doi: 10.1038/srep32224.
  26. Dizkirici A., Kansu C., Onde S., Murat M.B., Kaya O.Z. Phylogenetic relationships among Triticum and Aegilops L. species as genome progenitors of bread wheat based on sequence diversity in trnT-F region of chloroplast DNA // Genetic Resources and Crop Evolution. 2013. V.60. P.2227–2240. DOI: 10.1007/s10722-013-9988-x
  27. Dudnikov A.Ju. Chloroplast DNA non-coding sequences variation in Aegilops tauschii: evolutionary history of the species // Genetic Resources and Crop Evolution. 2012. V.59. P.683–699. doi:10.1007/s10722-011-9711-8
  28. Eilam T., Anikster Y., Millet E., Manisterski J., Sagi-Assif O., Feldman M. Genome size and genome evolution in diploid Triticeae species // Genome. 2007. V.50. P.1029-1037.
  29. El Baidouri M., Murat F., Veyssiere M., Molinier M., Flores R., Burlot L., Alaux M., Quesneville H., Pont C., Salse J. Reconciling the evolutionary origin of bread wheat (Triticum aestivum) // New Phytol. 2016 Aug 23. doi: 10.1111/nph.14113. [Epub ahead of print]
  30. Gogniashvili M., Jinjikhadze T., Maisaia I., Akhalkatsi M., Kotorashvili A., Kotaria N., Beridze T., Dudnikov A.J. Complete chloroplast genomes of Aegilops tauschii and Ae. cylindrica Host sheds light on plasmon D evolution // Curr. Genet. 2016. V.62. P.791-798.
  31. Gogniashvili M., Naskidashvili P., Bedoshvili D., Kotorashvili A., Kotaria N., Beridze T. Complete chloroplast DNA sequences of Zanduri wheat (Triticum ) // Genetic Resources and Crop Evolution. 2015. V. 62. P.1269–1277/ DOI: 10.1007/s10722-015-0230-x
  32. Goncharov N.P. Genus Triticum taxonomy: the present and the future // Plant Systematics and Evolution. 2011. V. 295, P.1–11.
  33. Goncharov N.P., Golovnina K.A., Kondratenko E.Ya. Taxonomy and molecular phylogeny of natural and artificial wheat species // Breeding Science. 2009. V.59. P. 492-498. doi:10.1270/jsbbs.59.492
  34. Gornicki P., Zhu H., Wang J., Challa G.S., Zhang Z., Gill B.S., Li W. The chloroplast view of the evolution of polyploid wheat // New Phytol. 2014 Nov;204(3):704-14. doi: 10.1111/nph.12931.
  35. Guo C.H., Terachi T. Variations in a hotspot region of chloroplast DNAs among common wheat and Aegilops revealed by nucleotide sequence analysis // Genes Genet Syst. 2005. V.80. P.277-285.
  36. Gupta P.K., Mir R.R., Mohan A., Kumar J. Wheat genomics: present status and future prospects // Int. J. Plant Genomics. 2008. 2008:896451. doi: 10.1155/2008/896451.
  37. Haider N. The origin of the B-genome of bread wheat (Triticum aestivum) // Genetika. 2013. V.49. P.303-314.
  38. He J., Zhao X., Laroche A., Lu Z.X., Liu H., Li Z. Genotyping-by-sequencing (GBS), an ultimate marker-assisted selection (MAS) tool to accelerate plant breeding // Front Plant Sci. 2014 Sep 30;5:484. doi: 10.3389/fpls.2014.00484.
  39. Hirosawa S., Takumi S., Ishii T., Kawahara T., Nakamura C., Mori N. Chloroplast and nuclear DNA variation in common wheat: insight into the origin and evolution of common wheat // Genes Genet. Syst. 2004. V.79. P.271-282.
  40. Huang Z., Long H., Wei Y.M., Yan Z.H., Zheng Y.L. Allelic variations of α-gliadin genes from species of Aegilops section Sitopsis and insights into evolution of α-gliadin multigene family among Triticum and Aegilops // Genetica. 2016. V.144. P.213-222. doi: 10.1007/s10709-016-9891-4.
  41. Jenkins J.A. Chromosome homologies in wheat and aegilops // American Journal of Botany. 1929. V. 16,. P. 238-245.
  42. Jia J., Zhao S., Kong X., Li Y., Zhao G., He W., Appels R., Pfeifer M., Tao Y., Zhang X., Jing R., Zhang C., Ma Y., Gao L., Gao C., Spannagl M., Mayer K.F., Li D., Pan S., Zheng F., Hu Q., Xia X., Li J., Liang Q., Chen J., Wicker T., Gou C., Kuang H., He G., Luo Y., Keller B., Xia Q., Lu P., Wang J., Zou H., Zhang R., Xu J., Gao J., Middleton C., Quan Z., Liu G., Wang J.; International Wheat Genome Sequencing Consortium., Yang H., Liu X., He Z., Mao L., Wang J. Aegilops tauschii draft genome sequence reveals a gene repertoire for wheat adaptation // Nature. 2013. V.496. P.91-95. doi: 10.1038/nature12028.
  43. International Wheat Genome Sequencing Consortium (IWGSC) A chromosome-based draft sequence of the hexaploid bread wheat (Triticum aestivum) genome // Science. 2014. V.345(6194):1251788. doi: 10.1126/science.1251788.
  44. Ishii T., Takahashi C., Ikeda N., Kamijima O., Mori N. Mitochondrial microsatellite variability in common wheat and its ancestral species // Genes Genet. Syst. 2006. V.81. P.211-214.
  45. Kihara H. Über cytologische Studien bei einigen Getreidearten // Bot. Mag. (Tokyo). 1919. V.33. S.17-38.
  46. Kimber G. A reassessment of the origin of the polyploid wheats // Genetics. 1974. V.78. P.487-492.
  47. Kornicke F. Der Weizen / Kornicke F., Werner H. Handbuch des Getreidebaus. Bonn-Berlin. S.22-114.
  48. Li L.F., Liu B., Olsen K.M., Wendel J.F. Multiple rounds of ancient and recent hybridizations have occurred within the Aegilops-Triticum complex // New Phytol. 2015. V.208. P.11-12. doi: 10.1111/nph.13563
  49. Li L.F., Liu B., Olsen K.M., Wendel J.F. A re-evaluation of the homoploid hybrid origin of Aegilops tauschii, the donor of the wheat D-subgenome // New Phytol. 2015. V.208. P.4-8. doi: 10.1111/nph.13294.
  50. Ling H.Q., Zhao S., Liu D., Wang J., Sun H., Zhang C., Fan H., Li D., Dong L., Tao Y., Gao C., Wu H., Li Y., Cui Y., Guo X., Zheng S., Wang B., Yu K., Liang Q., Yang W., Lou X., Chen J., Feng M., Jian J., Zhang X., Luo G., Jiang Y., Liu J., Wang Z., Sha Y., Zhang B., Wu H., Tang D., Shen Q., Xue P., Zou S., Wang X., Liu X., Wang F., Yang Y., An X., Dong Z., Zhang K., Zhang X., Luo M.C., Dvorak J., Tong Y., Wang J., Yang H., Li Z., Wang D., Zhang A., Wang J. Draft genome of the wheat A-genome progenitor Triticum urartu // Nature. 2013 Apr 4;496(7443):87-90. doi: 10.1038/nature11997.
  51. Linnaei C. Species plantarum / Holmiae [Stockholm]: L. Salvii, 1753. I. 560 p.
  52. Luo G., Zhang X., Zhang Y., Yang W., Li Y., Sun J., Zhan K., Zhang A., Liu D. Composition, variation, expression and evolution of low-molecular-weight glutenin subunit genes in Triticum urartu // BMC Plant Biol. 2015 Feb 28;15:68. doi: 10.1186/s12870-014-0322-3.
  53. Marcussen T., Sandve S.R., Heier L., Spannagl M., Pfeifer M.; International Wheat Genome Sequencing Consortium., Jakobsen K.S., Wulff B.B., Steuernagel B., Mayer K.F., Olsen O.A. Ancient hybridizations among the ancestral genomes of bread wheat // Science. V.345(6194):1250092. doi: 10.1126/science.1250092.
  54. Middleton C.P., Senerchia N., Stein N., Akhunov E.D., Keller B., Wicker T., Kilian B. Sequencing of chloroplast genomes from wheat, barley, rye and their relatives provides a detailed insight into the evolution of the Triticeae tribe // PLoS One. 2014 Mar 10;9(3):e85761. doi: 10.1371/journal.pone.0085761.
  55. Miyashita N.T., Mori N., Tsunewaki K. Molecular variation in chloroplast DNA regions in ancestral species of wheat // Genetics. V.137. P.883-889.
  56. Mochida K., Shinozaki K. Unlocking Triticeae genomics to sustainably feed the future // Plant Cell Physiol. 2013. V.54. P.1931-1950. doi: 10.1093/pcp/pct163.
  57. Nie X., Li B., Wang L., Liu P., Biradar S.S., Li T., Dolezel J., Edwards D., Luo M., Weining S. Development of chromosome-arm-specific microsatellite markers in Triticum aestivum (Poaceae) using NGS technology // Am. J. Bot. 2012. V.99. e369-71. doi: 10.3732/ajb.1200077.
  58. Ogihara, Y., Isono, K., Kojima, T. et al. Chinese spring wheat (Triticum aestivum) chloroplast genome: Complete sequence and contig clones // Plant Molecular Biology Reporter. 2000. V.18. P.243–253. DOI: 10.1007/BF02823995
  59. Ogihara Y., Isono K., Kojima T., Endo A., Hanaoka M., Shiina T., Terachi T., Utsugi S., Murata M., Mori N., Takumi S., Ikeo K., Gojobori T., Murai R., Murai K., Matsuoka Y., Ohnishi Y., Tajiri H., Tsunewaki K. Structural features of a wheat plastome as revealed by complete sequencing of chloroplast DNA // Mol. Genet. Genomics. 2002. V.266. P.740-746.
  60. Ogihara Y., Ohsawa T. Molecular analysis of the complete set of length mutations found in the plastomes of Triticum-Aegilops species // Genome. 2002. V.45. P.956-962.
  61. Ogihara Y, Tsunewaki K Diversity and evolution of chloroplast DNA in Triticum and Aegilops as revealed by restriction fragment analysis // Theor. Appl. Genet. 1988. V.76. P.321-332.
  62. Ogihara Y., Yamazaki Y., Murai K., Kanno A., Terachi T., Shiina T., Miyashita N., Nasuda S., Nakamura C., Mori N., Takumi S., Murata M., Futo S., Tsunewaki K. Structural dynamics of cereal mitochondrial genomes as revealed by complete nucleotide sequencing of the wheat mitochondrial genome // Nucleic Acids Res. 2005. V.33. P.6235-6250.
  63. Ozkan H., Levy A.A., Feldman M. Allopolypolidy-induced rapid genome evolution in the wheat (Aegilops-Triticum) group // Plant Cell. 2001. V.13. P.1745-1747.
  64. Ozkan H., Tuna M., Kilian B., Mori N., Ohta S. Genome size variation in diploid and tetraploid wild wheats // AoB Plants. 2010;2010:plq015. doi: 10.1093/aobpla/plq015.
  65. Percival J. The wheat plant. A monograph. 1921. 463 P.
  66. Reinisch A.J., Dong J.M., Brubaker C.L., Stelly D.M., Wendel J.F., Paterson A.H. A Detailed RFLP Map of Cotton, Gossypium Hirsutum X Gossypium Barbadense: Chromosome Organization and Evolution in a Disomic Polyploid Genome // Genetics. 1994. V.138. 829–847.
  67. Sakamura T. Kurze Mitteilung über die Chromosomen-zahlen und die Verwandtschaftsverhaltnisse der Triticum-arten // Bot. Mag. (Tokyo). 1918. V.32. S. 150-153. doi: 10.15281/jplantres1887.32.379_150
  68. Sandve S.R., Marcussen T., Mayer K., Jakobsen K.S., Heier L., Steuernagel B., Wulff B.B., Olsen O.A. Chloroplast phylogeny of Triticum/Aegilops species is not incongruent with an ancient homoploid hybrid origin of the ancestor of the bread wheat D-genome // New Phytol. V.208. P.9-10. doi: 10.1111/nph.13487.
  69. Sax K. Chromosome relationship in wheat // Science. V.54. P.413-415.
  70. Seringe N.C. Monographie des cereales de la Suisse / Bern. 1818.
  71. Schulz A. Die Geschichte der kultiverten Getreide. Halle. 1913.
  72. Stein N., Feuillet C., Wicker T., Schlagenhauf E., Keller B. Subgenome chromosome walking in wheat: a 450-kb physical contig in Triticum monococcum spans the Lr10 resistance locus in hexaploid wheat (Triticum aestivum L.) // Proc. Natl. Acad. Sci. USA. 2000. V.97. P.13436-13441.
  73. Terachi T., Ogihara Y., Tsunewaki K. The molecular basis of genetic diversity among cytoplasms of Triticum and Aegilops. 7. Restriction endonuclease analysis of mitochondrial DNAs from polyploid wheats and their ancestral species // Theor. Genet. 1990. V.80. P.366-373.
  74. de Tournefort J.P. Elemens de botanique ou methode pour connoitre les plantes / 1694. Tome 1. 307 p.
  75. Trick M., Adamski N.M., Mugford S.G., Jiang C.C., Febrer M., Uauy C. Combining SNP discovery from next-generation sequencing data with bulked segregant analysis (BSA) to fine-map genes in polyploid wheat // BMC Plant Biol. 2012 Jan 26;12:14. doi: 10.1186/1471-2229-12-14.
  76. Tsujimura M., Mori N., Yamagishi H., Terachi T. A possible breakage of linkage disequilibrium between mitochondrial and chloroplast genomes during Emmer and Dinkel wheat evolution // Genome. V.56. P.187-193. doi: 10.1139/gen-2012-0153.
  77. Tsunewaki K. Memoir on the origin of wheat stocks used by Prof. Tetsu Sakamura, on the centennial of his discovery of the correct chromosome number and polyploidy in wheat // Genes Genet. Syst. 2016. V.91. P.41-46. doi: 10.1266/ggs.15-00077.
  78. Vavilov N.I. The law of homologous series in variation // J. Gen. 1922. V.12. P. 47-90.
  79. Waines J.G., Barnhart D. Biosystematic research in Aegilops and Triticum // Hereditas. 1992. V.116. P.207-212.
  80. Wang G.-Z., Matsuoka Y., Tsunewaki K. Evolutionary features of chondriome divergence in Triticum (wheat) and Aegilops shown by RFLP analysis of mitochondrial DNAs // Theor. Appl. Genet. 2000. V.100. P.221–231.
  81. Wang G.Z., Miyashita N.T., Tsunewaki K. Plasmon analyses of Triticum (wheat) and Aegilops: PCR-single-strand conformational polymorphism (PCR-SSCP) analyses of organellar DNAs // Proc. Natl. Acad. Sci. USA. 1997. V.94. P.14570-1457.
  82. Watkins A.E. The wheat species: a critique // Journal of Genetics 1930. 23. P.173-263.
  83. Winkler H. Verbreitung und Ursache der Parthenogenesis im Pflanzen- und Tierreiche. 1920. Jena: Gustav Fischer Verlag. 250 s.
  84. Xie J., Huo N., Zhou S., Wang Y., Guo G., Deal K.R., Ouyang S., Liang Y., Wang Z., Xiao L., Zhu T., Hu T., Tiwari V., Zhang J., Li H., Ni Z., Yao Y., Peng H., Zhang S., Anderson O.D., McGuire P.E., Dvorak J., Luo M.C., Liu Z., Gu Y.Q., Sun Q. Sequencing and comparative analysis of Aegilops tauschii chromosome arm 3DS reveal rapid evolution of Triticeae genomes // J. Genet. 2016. Oct 5. pii: S1673-8527(16)30145-X. doi: 10.1016/j.jgg.2016.09.005. [Epub ahead of print]
  85. Xu L., Tang Y., Gao S., Su S., Hong L., Wang W., Fang Z., Li X., Ma J., Quan W., Sun H., Li X., Wang Y., Liao X., Gao J., Zhang F., Li L., Zhao C. Comprehensive analyses of the annexin gene family in wheat // BMC Genomics. 2016. May 28;17:415. doi: 10.1186/s12864-016-2750-y.
  86. Yuan J., Guo X., Hu J., Lv Z., Han F. Characterization of two CENH3 genes and their roles in wheat evolution // New Phytol. 2015. V.206. P.839-851. doi: 10.1111/nph.13235.
  87. Yamane K., Kawahara T. Intra- and interspecific phylogenetic relationships among diploid Triticum-Aegilops species (Poaceae) based on base-pair substitutions, indels, and microsatellites in chloroplast noncoding sequences // Am. J. Bot. 2005. V.92. P.1887-1898. doi: 10.3732/ajb.92.11.1887.
  88. Zhao S., Jiang Q.T., Ma J., Zhang X.W., Zhao Q.Z., Wang X.Y., Wang C.S., Cao X., Lu Z.X., Zheng Y.L., Wei Y.M. Characterization and expression analysis of WOX5 genes from wheat and its relatives // Gene. 2014. V.537. P.63-69. doi: 10.1016/j.gene.2013.12.022.
Download pdf
up
eISSN: 2221-6197 DOI: 10.31301/2221-6197