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dc.contributor.authorMagwanga, Richard
dc.contributor.authorLu, Pu
dc.contributor.authorKirungu, Joy
dc.contributor.authorDiouf, Latyr
dc.contributor.authorDong, Qi
dc.contributor.authorHu, Yangguang
dc.contributor.authorCai, Xiaoyan
dc.contributor.authorXu, Yanchao
dc.contributor.authorHou
dc.contributor.authorZhou, Zhongli
dc.contributor.authorWang, Xingxing
dc.contributor.authorWang, Kunbo
dc.contributor.authorLiu, Fang
dc.date.accessioned2021-04-14T09:07:54Z
dc.date.available2021-04-14T09:07:54Z
dc.date.issued2018-05-30
dc.identifier.urihttp://ir.jooust.ac.ke:8080/xmlui/handle/123456789/9458
dc.description.abstractCotton production is on the decline due to ever-changing environmental conditions. Drought and salinity stress contribute to over 30% of total loss in cotton production, the situation has worsened more due to the narrow genetic base of the cultivated upland cotton. The genetic diversity of upland cotton has been eroded over the years due to intense selection and inbreeding. To break the bottleneck, the wild cotton progenitors offer unique traits which can be introgressed into the cultivated cotton, thereby improving their performance. In this research, we developed a BC2F2 population between wild male parent, G. tomentosum as the donor, known for its high tolerance to drought and the elite female parent, G. hirsutum as the recurrent parent, which is high yielding but sensitive to drought stress. The population was genotyped through the genotyping by sequencing (GBS) method, in which 10,888 single-nucleotide polymorphism (SNP) s were generated and used to construct a genetic map. The map spanned 4191.3 cM, with average marker distance of 0.3849 cM. The map size of the two sub genomes had a narrow range, 2149 cM and 2042.3 cM for At and Dt_sub genomes respectively. A total of 66,434 genes were mined, with 32,032 (48.2%) and 34,402 (51.8%) genes being obtained within the At and Dt_sub genomes respectively. Pkinase (PF00069) was found to be the dominant domain, with 1069 genes. Analysis of the main sub family, serine threonine protein kinases through gene ontology (GO), cis element and miRNA targets analysis revealed that most of the genes were involved in various functions aimed at enhancing abiotic stress tolerance. Further analysis of the RNA sequence data and qRT-PCR validation revealed 16 putative genes, which were highly up regulated under drought stress condition, and were found to be targeted by ghr-miR169a and ghr-miR164, previously associated with NAC (NAM, ATAF1/2 and CUC2) and myeloblastosis (MYB), the top rank drought stress tolerance genes. These genes can be exploited further to aid in development of more drought tolerant cotton genotypes.en_US
dc.language.isoenen_US
dc.publisherMultidisciplinary Digital Publishing Instituteen_US
dc.subjectCottonen_US
dc.subjectDroughten_US
dc.subjectgenetic diversityen_US
dc.subjectgenotyping by sequencingen_US
dc.subjectbackcrossen_US
dc.titleGBS Mapping and Analysis of Genes Conserved between Gossypium tomentosum and Gossypium hirsutum Cotton Cultivars that Respond to Drought Stress at the Seedling Stage of the BC2F2 Generationen_US
dc.typeArticleen_US


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