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通过野生型基因拯救鉴定oda6为衣藻动力蛋白突变体。

Identification of oda6 as a Chlamydomonas dynein mutant by rescue with the wild-type gene.

作者信息

Mitchell D R, Kang Y

机构信息

Department of Anatomy and Cell Biology, State University of New York Health Science Center, Syracuse 13210.

出版信息

J Cell Biol. 1991 May;113(4):835-42. doi: 10.1083/jcb.113.4.835.

Abstract

We find that two Chlamydomonas outer arm dynein assembly loci, oda6 and oda9, are located on the left arm of linkage group XII, in the vicinity of the previously mapped locus for a 70,000 Mr dynein intermediate chain protein. Restriction fragment length polymorphism mapping indicates that this dynein gene is very closely linked to the oda6 locus. A cDNA clone encoding the 70,000 Mr protein was isolated, sequenced, and used to select genomic clones spanning the corresponding locus from both wild-type and oda6 libraries. When wild-type clones were introduced into cells containing an oda6 allele, the mutant phenotype was rescued, while no rescue was observed after transformation with oda6 clones. Genetic analysis further revealed that newly introduced gene copies were responsible for the rescued phenotype and thus confirms that ODA6 encodes the 70,000 Mr dynein intermediate chain protein. The inability of oda6 mutants to assemble any major outer arm dynein subunits shows that this protein is essential for assembly of stable outer dynein arms. This is the first use of transformation with a wild-type gene to identify the product of a Chlamydomonas mutant.

摘要

我们发现衣藻外臂动力蛋白装配位点oda6和oda9位于连锁群XII的左臂上,靠近先前定位的一个70,000道尔顿动力蛋白中间链蛋白的位点。限制性片段长度多态性图谱分析表明,该动力蛋白基因与oda6位点紧密连锁。分离并测序了编码70,000道尔顿蛋白的cDNA克隆,并用于从野生型和oda6文库中筛选跨越相应位点的基因组克隆。当将野生型克隆导入含有oda6等位基因的细胞中时,突变表型得到了挽救,而用oda6克隆转化后未观察到挽救现象。遗传分析进一步表明,新导入的基因拷贝导致了挽救的表型,从而证实ODA6编码70,000道尔顿的动力蛋白中间链蛋白。oda6突变体无法装配任何主要的外臂动力蛋白亚基,这表明该蛋白对于稳定的外动力蛋白臂的装配至关重要。这是首次利用野生型基因转化来鉴定衣藻突变体的产物。

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