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机构地区:[1]扬州大学农学院教育部植物功能基因组学重点实验室,江苏扬州225009
出 处:《植物生理学报》2013年第8期778-786,共9页Plant Physiology Journal
基 金:江苏省大学生实践创新训练计划项目(2012JSSPITP1409)
摘 要:从籼稻‘龙特甫B’来源的转基因后代中筛选获得一份淡黄叶突变体ygl-11,并对其进行了遗传分析和基因克隆研究。遗传分析表明,该淡黄叶突变性状受1对隐性核基因控制,并且与导入的T-DNA标签共分离。采用T-DNA标签的方法,从淡黄叶突变体植株中克隆了T-DNA插入位点的侧翼序列;序列分析表明T-DNA插入在水稻第11染色体OsGUN4基因5'非翻译区–103bp处。RT-PCR分析结果表明,突变体植株叶片中OsGUN4基因不表达;定量RT-PCR结果显示该基因在幼嫩的绿色叶片组织中表达量最高,在根和种子等组织中的表达极低。In present study, a novel yellow-green leaf mutant ygl-11 was selected from the transgenic progeny of the indica rice cultivar 'Longtefu B', and its genetic behavior as well as mutated gene was carefully studied. The leaf of the ygl-11 mutant is yellow during the whole growing periods. The mutation could be stably inherited according to the observation of several generations. The genetic analysis results indicated that the yellow-leaf mutation was controlled by a recessive gene and co-segregated with the integrated T-DNA in ygl-11 mutant. By using the inverse- and TAIL-PCR methods with minor modification, the flanking genomic sequence of the T-DNA insertion was cloned from the mutant. After alignment between the cloned sequences and rice genomic sequences, the T-DNA was identified to insert into the 5'-untranslational region of the OsGUN4 gene on chromosome 11. The result of semi-quantitative RT-PCR revealed that there was no expression of the OsGUN4 gene inygl-11 mutant. Real-time RT-PCR analysis showed that the OsGUN4 gene highly expresses in green tissue of wild type rice, but very low in root and seed.
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