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首页> 外文期刊>Nucleic acids research >Transcripts of the ndhH–D operon of barley plastids: possible role of unedited site III in splicing of the ndhA intron
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Transcripts of the ndhH–D operon of barley plastids: possible role of unedited site III in splicing of the ndhA intron

机译:大麦质体ndhH–D操纵子的转录本:未编辑位点III在ndhA内含子剪接中的可能作用

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摘要

The plastid ndhH–D operon produces several transcripts containing ndhA sequence with and without its group II intron. After sequencing an 8125 bp fragment of barley plastid DNA including the ndhH–D operon, we investigated the editing–splicing status of transcripts in the range 1.0–7.8 kb. Reverse transcription and sequencing of RNA bands separated by electrophoresis were used to determine C→U editing sites. Sites I, II and IV of ndhA and site V of ndhD were edited in all transcripts analysed and, probably, were edited before any splicing had taken place. In contrast, site III of ndhA (13 bp from the 5′-end base of the second exon) was not edited in transcripts containing the intron (including the 1.7 kb inter-mediary transcript consisting of the intron and the second exon) but was edited in all transcripts lacking the ndhA intron. Comparison of the secondary structures of the ndhA intron and intron–second exon intermediate suggests that G pairing prevents editing of site III in transcripts containing the intron and maintains the secondary structure required for splicing. Splicing of the ndhA intron releases the site?III C from pairing and, probably, brings it close to cis- acting elements for editing upstream in the first exon.
机译:质体的ndhH–D操纵子会产生包含ndhA序列的多个转录物,带有或不带有II组内含子。对包括ndhH–D操纵子的大麦质体DNA的8125 bp片段进行测序后,我们研究了1.0–7.8 kb范围内转录本的编辑-剪接状态。通过电泳分离的RNA条带的反转录和测序被用于确定C→U编辑位点。在所有已分析的转录本中,编辑了ndhA的I,II和IV位以及ndhD的V位,并且很可能在进行任何剪接之前进行了编辑。相反,ndhA的位点III(距离第二个外显子的5'端碱基13 bp)在包含内含子的转录本(包括由内含子和第二个外显子组成的1.7 kb中介转录本)中未被编辑,但是编辑了所有缺少ndhA内含子的转录本。比较ndhA内含子和内含子-第二外显子中间体的二级结构表明,G配对可防止编辑包含内含子的转录本中的位点III,并维持剪接所需的二级结构。 ndhA内含子的剪接可将位点III C解除配对,并可能使其接近顺式作用元件以在第一个外显子的上游进行编辑。

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