[Identification of molecular markers linked to the fertility restoring gene for the CMS Capsicum annuum L].

Shi yan sheng wu xue bao Pub Date : 2005-06-01
Cai Tao Chang, Chun Guo Wang, Cheng Bin Chen, Feng Wu, De Ling Sun
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Abstract

Bulked segregant analysis method was used to identify random amplified polymorphic DNA (RAPD) markers linked to the fertility restoring gene for the cytoplasmic male sterility (CMS) capsicum annum L. Totally 336 random primers were screened on the DNA samples of restorer and sterile bulks. Primer S418 produced a special band in restorer line. It was about 3000 bp, including two fragments 1515 bp and 1162 bp. Fluorescence in situ hybridization(FISH) indicated the fragment of 1515 bp only existed in restorer line.It was designed to S418(1515). Analysis of the sequence indicated S418(1515) was unknown before. The homology of blastn was less than 40%, however the homology of tBlastx indicated this sequence was high homologous with the part sequences of rice which were distributed on 2,4,7,10 chromosomes. It suggested this sequence might have the similar function with them. This result offered a good foundation to research the molecular mechanism of fertility restoration for CMS capsicum. Based on the sequence, special primers were designed to transform the RAPD marker to PCR marker. The result indicated that these primers could be used to screen the restorer lines from a large quantitive of candidate lines.

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[CMS辣椒育性恢复基因分子标记的鉴定]。
采用散装分离分析方法,鉴定了辣椒细胞质雄性不育(CMS)育性恢复基因的随机扩增多态性DNA (RAPD)标记,共筛选到336个随机引物,分别用于恢复系和不育系的DNA样品。引物S418在恢复系中产生特殊条带。全长约3000 bp,包括1515 bp和1162 bp两个片段。荧光原位杂交(FISH)结果表明,1515bp的片段仅存在于恢复系中。它被设计成1818年(1515年)。序列分析表明S418(1515)是未知的。该序列与水稻2、4、7、10条染色体上的部分序列具有高度的同源性。这表明该序列可能与它们具有相似的功能。该结果为研究CMS辣椒育性恢复的分子机制提供了良好的基础。根据该序列设计专用引物,将RAPD标记转化为PCR标记。结果表明,这些引物可用于从大量候选系中筛选恢复系。
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