首页> 外文期刊>African Journal of Biotechnology >Studies on some major yield responsive genes in selected rice (Oryza species) cultivars grown in Nigeria using candidate gene SSR-based markers approach
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Studies on some major yield responsive genes in selected rice (Oryza species) cultivars grown in Nigeria using candidate gene SSR-based markers approach

机译:基于候选基因SSR的标记方法在尼日利亚种植的选定水稻(Oryza物种)品种中的一些主要产量反应基因的研究

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This study was aimed at determining the presence of five major yield responsive genes shown to be among key determinants of rice yield in ten rice cultivars grown in Nigeria using candidate gene SSRs markers (Cg-SSRs). DNAs were extracted from young leaf samples using optimized cetyltrimethylammonium bromide (CTAB)-extraction method. An established gene sequences for high yielding rice Nipponbare cultivar for the five genes were retrieved from NCBI database and used to mine for SSRS using SSR identification tool. A pair of primer were designed manually from the nucleotide sequences flanking the selected SSRS for each gene. The designed primers were used to screen for the presence of the genes. Three pair of primers (for Gif1, Gn1a and Gw2) were able to amplify the targeted regions. The remaining two (for Gs3 and Dep1) did not amplify even the positive control. Two representative polymerase chain reaction (PCR)-products for the PCR-positive genes were sequenced and compared with established gene sequences of high yielding cultivars on NCBI database and their percentage sequence identities were determined. Phylogenetic trees (dendrograms) were generated using neighbor joining method. Overall, all the ten cultivars have both Gif1 and Gn1a genes while only eight cultivars have Gw2 gene. Gs3 and Dep1 need further optimization of PCR-conditions.
机译:该研究旨在确定尼日利亚在尼日利亚生长的10种大米品种的主要决定因素中存在五个主要产量响应基因的存在,使用候选基因SSR标记物(CG-SSRS)。使用优化的十六烷基三甲基溴化铵(CTAB) - 萃取方法从幼叶样品中提取DNA。从NCBI数据库中检索了对五个基因的高产米尼比布栽培品种的已建立的基因序列,并使用SSR识别工具用于SSRS。从侧翼所选择的SSR的核苷酸序列手动设计一对引物。设计的引物用于筛选基因的存在。三对引物(对于GIF1,GN1A和GW2)能够扩增靶区域。剩下的两个(对于GS3和DEP1)甚至没有放大阳性对照。对PCR阳性基因的两个代表性聚合酶链反应(PCR)进行测序,并与NCBI数据库的高产品种的已建立的基因序列进行比较,确定其百分比序列同一性。使用邻近加入方法产生系统发育树(树枝图)。总体而言,所有10种品种都有GIF1和GN1A基因,而只有八种品种具有GW2基因。 GS3和DEP1需要进一步优化PCR条件。

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