水稻线粒体rps10基因向细胞核的转移:获得5'非翻译区,随后进行基因复制。

N Kubo, X Jordana, K Ozawa, S Zanlungo, K Harada, T Sasaki, K Kadowaki
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引用次数: 42

摘要

线粒体核糖体蛋白S10 (rps10)由马铃薯和豌豆的线粒体基因组编码。在这里,我们发现rps10基因在水稻的线粒体基因组中缺失,并且已经转移到细胞核中。克隆和转录分析表明,水稻核基因组中存在两个rps10基因,它们的转录产物丰度不同。Western分析在水稻线粒体的可溶部分检测到RPS10蛋白,尽管两种RPS10都没有明显的靶向线粒体的n端序列。这一结果表明,水稻RPS10的内部区域存在靶向信息。基因组序列分析表明,每个rps10基因在5'非翻译区(5' UTR)都有一个内含子,这些内含子序列彼此同源。这一结果强烈表明rps10基因转移到细胞核后发生了复制事件。通过RFLP分析,两个rps10基因分别位于第6号和第12号染色体上,因此重复的rps10基因已被易位到不同的染色体上。有趣的是,水稻rps10基因的5' UTR和内含子与几种具有不同功能的水稻基因(如osk4、EF-1beta2和RAG1)中的序列同源,这表明5' UTR具有共同的起源和功能作用。获得5'侧区可能加速了线粒体rps10基因的激活,并将其转移到核基因组中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Transfer of the mitochondrial rps10 gene to the nucleus in rice: acquisition of the 5' untranslated region followed by gene duplication.

Mitochondrial ribosomal protein S10 (rps10) is encoded by the mitochondrial genome in potato and pea. Here we show that the rps10 gene is absent from the mitochondrial genome of rice and has been transferred to the nucleus. Cloning and transcriptional analysis show that there are two rps10 genes in the rice nuclear genome and that their transcripts differ in abundance. Western analysis detected the RPS10 protein in the soluble fraction of rice mitochondria, although neither RPS10 has any obvious N-terminal presequence for targeting to mitochondria. This result suggests that targeting information is present in the internal region of rice RPS10. Genomic sequence analysis indicated that each rps10 gene has an intron in the 5' untranslated region (5' UTR) and that these intron sequences are homologous to each other. This result strongly suggests that a duplication event occurred after transfer of the rps10 gene to the nucleus. The duplicated rps10 genes have since been translocated to different chromosomes, because the two rps10 genes were mapped on chromosomes 6 and 12 by RFLP analysis. Interestingly, the 5' UTR and the intron of the rice rps10 genes are homologous to sequences found in several rice genes with various functions, such as osk4, EF-1beta2 and RAG1, suggesting a common origin and a functional role for the 5' UTR. Acquisition of the 5' flanking region might have accelerated the activation of the mitochondrial rps10 gene which was transferred to the nuclear genome.

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