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锥虫中的RNA编辑。向导RNA的作用。

RNA editing in trypanosomes. The us(e) of guide RNAs.

作者信息

Benne R

机构信息

E.C. Slater Institute for Biochemical Research, University of Amsterdam, The Netherlands.

出版信息

Mol Biol Rep. 1992 Sep;16(4):217-27. doi: 10.1007/BF00419661.

DOI:10.1007/BF00419661
PMID:1454054
Abstract

Guide RNAs are encoded in maxicircle and minicircle DNA of trypanosome mitochondria. They play a pivotal role in RNA editing, a process during which the nucleotide sequence of mitochondrial RNAs is altered by U-insertion and deletion. Guide RNAs vary in length from 35 to 78 nucleotides, which correlates with the variation in length of the three functionally important regions of which they are composed: (i) a 4-14 nucleotide 'anchor' sequence embedded in the 5' region, which is complementary to a target sequence on the pre-edited RNA downstream of an editing domain, (ii) a middle part containing the editing information, which ranges from guiding the insertion of just one U into one site to that of the insertion of 32 Us into 10 sites, and (iii) a 5-24 nucleotide 3' terminal oligo [U] extension. Moreover, a variable uridylation site creates gRNAs containing a varying segment of editing information for the same domain. Comparison of different guide RNAs demonstrates that, besides the U-tail, they have no obvious common primary and secondary sequence motifs, each particular sequence being unique. The occurrence in vivo and the synthesis in vitro of chimeric molecules, in which a guide RNA is covalently linked through its 3' U-tail to an editing site of a pre-edited RNA, suggests that RNA editing occurs by consecutive transesterification reactions and is evidence that the guide RNAs not only provide the genetic information, but also the Us themselves.

摘要

引导RNA由锥虫线粒体的大环和小环DNA编码。它们在RNA编辑中起关键作用,在这个过程中,线粒体RNA的核苷酸序列通过U的插入和缺失而改变。引导RNA的长度从35到78个核苷酸不等,这与它们所组成的三个功能重要区域的长度变化相关:(i)嵌入5'区域的4-14个核苷酸的“锚定”序列,它与编辑结构域下游的预编辑RNA上的靶序列互补;(ii)包含编辑信息的中间部分,其范围从引导仅一个U插入一个位点到引导32个U插入10个位点;(iii)一个5-24个核苷酸的3'末端寡聚[U]延伸。此外,一个可变的尿苷酸化位点产生了针对同一结构域包含不同编辑信息片段的引导RNA。不同引导RNA的比较表明,除了U尾外,它们没有明显的共同一级和二级序列基序,每个特定序列都是独特的。体内出现以及体外合成的嵌合分子,其中引导RNA通过其3' U尾与预编辑RNA的编辑位点共价连接,这表明RNA编辑是通过连续的转酯反应发生的,并且证明引导RNA不仅提供遗传信息,而且还提供U本身。

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