Genetic and physical fine mapping of a multilocular gene Bjln1 in Brassica juncea to a 208-kb region
文献类型： 外文期刊
作者： Xiao, Lu 1 ; Zhao, Huiyan 1 ; Zhao, Zhi 1 ; Du, Dezhi 1 ; Xu, Liang 1 ; Yao, Yanmei 2 ; Zhao, Zhigang; Xing, Xiaorong; 1 ;
作者机构： 1.Qinghai Acad Agr & Forestry Sci, Key Lab Spring Rape Genet Improvement Qinghai Pro, Natl Key Lab Breeding Base Innovat & Utilizat Pla, Xining 810016, Qinghai, Peoples R China
2.Qinghai Acad Agr & Forestry Sci, Key Lab Spring Rape Genet Improvement Qinghai Pro, Natl Key Lab Breeding Base Innovat & Utilizat Pla, Xining 81
关键词： Brassica juncea;Locule number;SSR;Synteny;Fine mapping
期刊名称：MOLECULAR BREEDING （ 影响因子：2.589； 五年影响因子：2.75 ）
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收录情况： SCI
摘要： Most of the germplasm resources in Brassica juncea produce silique with only two locules, whereas a few varieties can produce silique with three or four locules. The increase in locule number in B. juncea has been shown to cause an increase in the number of seeds per silique, resulting in an increase in the yield per plant. Thus, the development of high-locule-number varieties may be an effective way of improving the yield of B. juncea. Duoshi, a B. juncea landrace originating from the Qinghai-Tibetan plateau, produces silique with 3-4 locules. Genetic analysis has shown that the high-locule-number trait in Duoshi is determined by two recessive genes, tentatively designated as Bjln1 and Bjln2. For fine mapping of the Bjln1 gene, a BC3 population was developed from the cross between Duoshi (multilocular parent) and Xinjie (bilocular parent). Using a combination of amplified fragment length polymorphism (AFLP) and bulked segregant analysis, only two AFLP markers linked to Bjln1 were identified. Preliminary linkage analysis showed that the two AFLP markers were located on the same side of Bjln1. Blast analysis revealed that the sequences of the two AFLP markers had homologues on Scaffold000019 at the bottom of B. rapa A7. Using the results of linkage analysis and BlastN searches, simple sequence repeat (SSR) markers were subsequently developed based on the sequence information from B. rapa A7. Seven SSR markers were eventually identified, of which ln 8 was co-segregated with Bjln1. ln 7 and ln 9, the closest flanking markers, were mapped at 2.0 and 0.4 cM distant from the Bjln1 gene, respectively. The SSR markers were cloned, sequenced and mapped on A7 of B. rapa (corresponding to J7 in the A genome of B. juncea). The two closest flanking markers, ln 7 and ln 9, were mapped within a 208-kb genomic region on B. rapa A7, in which the Bjln1 gene might be included. The present study may facilitate cloning of the Bjln1 gene as well as the selection process for developing multilocular varieties in B. juncea by marker-assisted selection and genetic engineering.
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