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小麦线粒体中编码NADH脱氢酶亚基4的转录本的RNA编辑:编辑位点在四个外显子间分布不均。

RNA editing of the transcript coding for subunit 4 of NADH dehydrogenase in wheat mitochondria: uneven distribution of the editing sites among the four exons.

作者信息

Lamattina L, Grienenberger J M

机构信息

Institut de Biologie Moléculaire des Plantes du CNRS, Université Louis Pasteur, Strasbourg, France.

出版信息

Nucleic Acids Res. 1991 Jun 25;19(12):3275-82. doi: 10.1093/nar/19.12.3275.

Abstract

The wheat mitochondrial (mt) NADH dehydrogenase subunit 4 gene (nad4) has been localized and sequenced. This gene, about 8 kb long, is composed of four exons separated by three class II introns. The nad4 gene exists as a single copy in the wheat mitochondrial genome and it is transcribed into one abundant mRNA of 1.8 kb, whose extremities have been mapped. The complete cDNA sequence corresponding to the nad4 transcript has been determined by combining the direct sequencing of uncloned cDNA and a method involving cDNA synthesis and PCR amplification using specific oligonucleotides as primers, followed by cloning and sequencing of the amplification product. Comparison of the genomic sequence with that of the cDNA shows that all nad4 transcripts are fully edited at 23 positions, with an uneven distribution of the editing sites between the different exons: While exon 1 and exon 4 are extensively edited (with a change of 11% of the amino acid sequence), exon 2 is not edited at all and exon 3 is 0.5% edited. This uneven distribution is discussed.

摘要

小麦线粒体(mt)烟酰胺腺嘌呤二核苷酸脱氢酶亚基4基因(nad4)已被定位和测序。该基因长度约为8 kb,由四个外显子组成,中间被三个II类内含子隔开。nad4基因在小麦线粒体基因组中以单拷贝形式存在,转录成一个1.8 kb的丰富mRNA,其末端已被定位。通过将未克隆的cDNA直接测序与一种涉及cDNA合成和使用特定寡核苷酸作为引物的PCR扩增方法相结合,随后对扩增产物进行克隆和测序,确定了与nad4转录本相对应的完整cDNA序列。基因组序列与cDNA序列的比较表明,所有nad4转录本在23个位置上都经过了完全编辑,不同外显子之间编辑位点的分布不均匀:外显子1和外显子4经过广泛编辑(氨基酸序列变化11%),外显子2完全不编辑,外显子3编辑率为0.5%。本文讨论了这种不均匀分布。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d51f/328322/8572808fdd57/nar00092-0096-a.jpg

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