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人类线粒体中重叠转运RNA的加工与编辑

Processing and editing of overlapping tRNAs in human mitochondria.

作者信息

Reichert A, Rothbauer U, Mörl M

机构信息

Max-Planck-Institute for Evolutionary Anthropology, Institute of Zoology, University of Munich, Luisenstrasse 14, 80333 Munich, Germany.

出版信息

J Biol Chem. 1998 Nov 27;273(48):31977-84. doi: 10.1074/jbc.273.48.31977.

DOI:10.1074/jbc.273.48.31977
PMID:9822669
Abstract

Overlapping tRNA genes in mitochondria of many metazoans introduce a problem for the processing of such polycistronic primary transcripts. Using runoff transcripts and an S100 extract from HeLa cell mitochondria, the processing of the human mitochondrial tRNATyr/tRNACys precursor (carrying an overlap of one base) was investigated: tRNACys is released in its complete form carrying the overlapping residue at the first position, whereas tRNATyr lacks that nucleotide at the discriminator position. Partial deletion of tRNACys or complete replacement by a non-tRNA-like sequence does not alter the processing reaction and indicates that the upstream tRNATyr alone is recognized by a 3'-endonuclease activity. The truncated 3'-end of this tRNATyr is then completed in an editing reaction that incorporates the missing residue. The processing of this tRNA overlap seems to be species-specific, because an overlapping tRNA precursor (tRNASer(AGY)/tRNALeu(CUN)) from opossum mitochondria is not recognized by the human extract. Because processing activities for overlapping and nonoverlapping tRNA precursors could not be separated, it seems that one general activity is responsible for the 3'-end processing of mitochondrial tRNAs and that this activity coevolved with the particular overlap between tRNATyr and tRNACys in human mitochondria, being unable to recognize overlaps between other tRNAs.

摘要

许多后生动物线粒体中的重叠tRNA基因给此类多顺反子初级转录本的加工带来了问题。利用从人宫颈癌(HeLa)细胞线粒体中获得的连续转录本和S100提取物,对人线粒体tRNATyr/tRNACys前体(携带一个碱基的重叠)的加工进行了研究:tRNACys以完整形式释放,在第一位携带重叠残基,而tRNATyr在鉴别位点缺少该核苷酸。tRNACys的部分缺失或被非tRNA样序列完全取代不会改变加工反应,这表明上游的tRNATyr单独被一种3'-核酸内切酶活性识别。然后,这种tRNATyr的截短3'-末端在一个编辑反应中完成,该反应掺入缺失的残基。这种tRNA重叠的加工似乎具有物种特异性,因为来自负鼠线粒体的重叠tRNA前体(tRNASer(AGY)/tRNALeu(CUN))不被人提取物识别。由于重叠和非重叠tRNA前体的加工活性无法分离,似乎一种普遍的活性负责线粒体tRNA的3'-末端加工,并且这种活性与人线粒体中tRNATyr和tRNACys之间的特定重叠共同进化,无法识别其他tRNA之间的重叠。

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