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Morphological, cytological and molecular analyses of a synthetic hexaploid derived from an interspecific hybrid between Gossypium hirsutum and Gossypium anomalum

Xia ZhangThe Institute of Industrial Crops, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, ChinaCaijiao ZhaiThe Institute of Industrial Crops, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, ChinaLinchi HeQi GuoThe Institute of Industrial Crops, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, ChinaXianggui ZhangKey Laboratory of Cotton and Rapeseed, Ministry of Agriculture, Nanjing, ChinaPeng XuThe Institute of Industrial Crops, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, ChinaHongmei SuThe Institute of Industrial Crops, Jiangsu Academy of Agricultural Sciences, Nanjing 210014, ChinaYuan‐Yong GongKey Laboratory of Cotton and Rapeseed, Ministry of Agriculture, Nanjing, ChinaNI Wan-chaoKey Laboratory of Cotton and Rapeseed, Ministry of Agriculture, Nanjing, ChinaXinlian ShenKey Laboratory of Cotton and Rapeseed, Ministry of Agriculture, Nanjing, China
2014en
ABI

Annotatsiya

Gossypium anomalum represents an inestimable source of genes that could potentially be transferred into the gene pool of cultivated cotton. To resolve interspecific hybrid sterility problems, we previously treated triploid hybrids derived from a cross between Gossypium hirsutum and G. anomalum with 0.15% colchicine and obtained a putative fertile hexaploid. In this study, we performed morphological, molecular and cytological analyses to assess the hybridity and doubled status of putative interspecific hybrid plants. Most of the morphological characteristics of the putative hexaploid plants were intermediate between G. hirsutum and G. anomalum. Analysis of mitotic metaphase plates revealed 78 chromosomes, confirming the doubled hybrid status of the hexaploid. Genome-wide molecular analysis with different genome-derived SSR markers revealed a high level of polymorphism (96.6%) between G. hirsutum and G. anomalum. The marker transferability rate from other species to G. anomalum was as high as 98.0%. The high percentage of polymorphic markers with additive banding profiles in the hexaploid indicates the hybridity of the hexaploid on a genome-wide level. A-genome-derived markers were more powerful for distinguishing the genomic differences between G. hirsutum and G. anomalum than D-genome-derived markers. This study demonstrates the hybridity and chromosomally doubled status of the (G. anomalum × G. hirsutum)2 hexaploid using morphological, cytological and molecular marker methods. The informative SSR markers screened in the study will be useful marker resources for tracking the flow of G. anomalum genetic material among progenies that may be produced by future backcrosses to G. hirsutum.

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