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[苎麻(Boehmeria nivea (L.) Gaud.)atp6和atp9基因的克隆、表达及其与细胞质雄性不育的关系]

[Cloning and expression of atp6 and atp9 genes from ramie (Boehmeria nivea (L.) Gaud.) and their relationship with cytoplasmic male sterility].

作者信息

Duan Ji-Qiang, DU Guang-Hui, Li Jian-Yong, Liang Xue-Ni, Liu Fei-Hu

机构信息

Laboratory of Plant Improvement and Utilization, Yunnan University, Kunming 650091, China.

出版信息

Yi Chuan. 2008 Nov;30(11):1487-98. doi: 10.3724/sp.j.1005.2008.01487.

Abstract

The atp6 and apt9 gene fragments associated with cytoplasmic male sterility (CMS) were cloned from the mitochondrial DNA of a ramie (Boehmeria nivea (L.) Gaud.) cytoplasmic male sterile line and its maintainer and restorer lines using PCR and degenerated primer strategy. The primers were designed according to the reserved sequences in the encoding region of mitochondrial genes atp6 and atp9 of some dicotyledons from GenBank. These fragments did not have complete encoding region but showed the homology of 94% and 85% with atp6 and atp9 genes from the referred dicotyledons in GenBank. The complete atp6 and atp9 genes including the complete open reading frames were cloned by means of amplifying the 3' and 5'end unknown sequences of these gene fragments using DNA Walking method. The atp6 gene showed no difference among ramie male sterile line, maintainer and restorer lines at mtDNA sequence, transcription and translation control and protein level. However, compared to the maintainer and restorer lines, the atp9 gene of the male sterile line was different and deletion in several bases at the 3' end of the encoding region. An abnormally high expression of atp9 gene in the male sterile line at the budding stage and full-bloom stage was analyzed by RT-PCR analysis. These results indicated that the variation in DNA sequence and/or abnormality in expression of atp9 gene in the male sterile line maybe closely related to ramie CMS.

摘要

采用PCR和简并引物策略,从苎麻(Boehmeria nivea (L.) Gaud.)细胞质雄性不育系及其保持系和恢复系的线粒体DNA中克隆了与细胞质雄性不育(CMS)相关的atp6和apt9基因片段。根据GenBank中一些双子叶植物线粒体基因atp6和atp9编码区的保守序列设计引物。这些片段没有完整的编码区,但与GenBank中参考双子叶植物的atp6和atp9基因具有94%和85%的同源性。通过DNA步移法扩增这些基因片段的3'和5'端未知序列,克隆了包括完整开放阅读框的完整atp6和atp9基因。atp6基因在苎麻雄性不育系、保持系和恢复系的mtDNA序列、转录和翻译调控以及蛋白质水平上没有差异。然而,与保持系和恢复系相比,雄性不育系的atp9基因存在差异,其编码区3'端有几个碱基缺失。通过RT-PCR分析,发现雄性不育系在现蕾期和盛花期atp9基因表达异常高。这些结果表明,雄性不育系中atp9基因的DNA序列变异和/或表达异常可能与苎麻CMS密切相关。

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