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对改变的线粒体atp6 RNA进行处理并完全编辑后可恢复细胞质雄性不育水稻的育性。

Processing followed by complete editing of an altered mitochondrial atp6 RNA restores fertility of cytoplasmic male sterile rice.

作者信息

Iwabuchi M, Kyozuka J, Shimamoto K

机构信息

Plantech Research Institute, Yokohama, Japan.

出版信息

EMBO J. 1993 Apr;12(4):1437-46. doi: 10.1002/j.1460-2075.1993.tb05787.x.

Abstract

Two atp6 genes were found in the mitochondrial genome of cytoplasmic male sterile (CMS) rice carrying the [cms-bo] cytoplasm. One (N-atp6) was identical to the normal cytoplasmic gene, while the second (B-atp6) was identified as a candidate CMS gene by Southern analysis of the mitochondrial genome of CMS cybrid rice. The coding sequence of B-atp6 was identical to the normal N-atp6 gene but its 3'-flanking sequence was different starting at 49 bases downstream from the stop codon. Northern analysis showed that B-atp6 is transcribed into a 2.0 kb RNA in the absence of the Rf-1 gene, whereas two discontinuous RNAs, of approximately 1.5 and 0.45 kb, were detected in the presence of the Rf-1 gene. Determination of the 3' and 5' ends of these RNAs suggested that the two discontinuous RNAs were generated from the 2.0 kb RNA by RNA processing at sites within the B-atp6-specific sequences by the action of the Rf-1 gene. Sequence analysis of cDNA clones derived from the N-atp6 RNA and the processed and unprocessed RNAs of B-atp6 indicated that the processed B-atp6 RNAs were edited as efficiently as the N-atp6, whereas unedited and partially edited RNAs were detected among unprocessed RNAs. RNA processing by Rf-1 thus influences the sequential post-transcriptional editing of the B-atp6 RNAs. Because the unprocessed RNAs of B-atp6 are possibly translated into altered polypeptides, our results suggest that interaction of RNA processing and editing plays a role in controlling CMS expression and the restoration of fertility in rice.

摘要

在携带[cms-bo]细胞质的细胞质雄性不育(CMS)水稻的线粒体基因组中发现了两个atp6基因。其中一个(N-atp6)与正常细胞质基因相同,而另一个(B-atp6)通过对CMS体细胞杂种水稻线粒体基因组的Southern分析被鉴定为候选CMS基因。B-atp6的编码序列与正常的N-atp6基因相同,但其3'侧翼序列在终止密码子下游49个碱基处开始不同。Northern分析表明,在没有Rf-1基因的情况下,B-atp6转录成2.0 kb的RNA,而在有Rf-1基因的情况下,检测到两条不连续的RNA,大小约为1.5 kb和0.45 kb。这些RNA的3'和5'末端的测定表明,这两条不连续的RNA是由Rf-1基因的作用在B-atp6特异性序列内的位点通过RNA加工从2.0 kb的RNA产生的。对来自N-atp6 RNA以及B-atp6加工和未加工RNA的cDNA克隆的序列分析表明,加工后的B-atp6 RNA与N-atp6一样有效地被编辑,而在未加工的RNA中检测到未编辑和部分编辑的RNA。因此,Rf-1介导的RNA加工影响了B-atp6 RNA的顺序转录后编辑。由于B-atp6的未加工RNA可能被翻译成改变的多肽,我们的结果表明RNA加工和编辑的相互作用在控制水稻CMS表达和育性恢复中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/153b/413355/ef83efe7fea8/emboj00076-0182-a.jpg

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