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核基因对细胞质雄性不育的抑制作用改变了一个新的线粒体基因区域的表达。

Suppression of cytoplasmic male sterility by nuclear genes alters expression of a novel mitochondrial gene region.

作者信息

Singh M, Brown G G

机构信息

Department of Biology, McGill University, Montreal, Quebec, Canada.

出版信息

Plant Cell. 1991 Dec;3(12):1349-62. doi: 10.1105/tpc.3.12.1349.

Abstract

To identify regions of the mitochondrial genome that potentially could specify the "Polima" (pol) cytoplasmic male sterility (CMS) of Brassica napus, transcripts of 14 mitochondrial genes from nap (male fertile), pol (male sterile), and nuclear fertility-restored pol cytoplasm plants were analyzed. Transcriptional differences among these plants were detected only with the ATPase subunit 6 (atp6) gene. Structural analysis of the atp6 gene regions of pol and nap mitochondrial DNAs showed that rearrangements in the pol mitochondrial genome occurring upstream of atp6 have generated a chimeric 224-codon open reading frame, designated orf224, that is cotranscribed with atp6. In CMS plants, most transcripts of this region are dicistronic, comprising both orf224 and atp6 sequences. Nuclear restorer genes at either of two distinct loci appear to specifically alter this transcript pattern such that monocistronic atp6 transcripts predominate. The differences in expression of this region appear to result, in part, from differential processing of a tRNA-like element comprising a tRNA pseudogene present immediately upstream of atp6 in both the sterile and fertile mitochondrial DNAs. Possible mechanisms by which expression of the orf224/atp6 locus and the Polima CMS trait may be specifically related are considered.

摘要

为了确定油菜线粒体基因组中可能决定“波里马”(pol)细胞质雄性不育(CMS)的区域,对来自nap(雄性可育)、pol(雄性不育)和核育性恢复的pol细胞质植株的14个线粒体基因的转录本进行了分析。仅在ATP酶亚基6(atp6)基因上检测到了这些植株之间的转录差异。对pol和nap线粒体DNA的atp6基因区域进行结构分析表明,pol线粒体基因组中atp6上游发生的重排产生了一个嵌合的224密码子开放阅读框,命名为orf224,它与atp6共转录。在CMS植株中,该区域的大多数转录本是双顺反子的,包含orf224和atp6序列。两个不同位点之一的核恢复基因似乎特异性地改变了这种转录模式,使得单顺反子atp6转录本占主导。该区域表达的差异似乎部分源于对一个类似tRNA元件的不同加工,该元件由不育和可育线粒体DNA中atp6上游紧邻的一个tRNA假基因组成。文中考虑了orf224/atp6位点的表达与波里马CMS性状可能具体相关的潜在机制。

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