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11种昆虫基因组中的剪接体小核RNA基因

Spliceosomal small nuclear RNA genes in 11 insect genomes.

作者信息

Mount Stephen M, Gotea Valer, Lin Chiao-Feng, Hernandez Kristina, Makalowski Wojciech

机构信息

Department of Cell Biology and Molecular Genetics, University of Maryland, College Park, Maryland 20742-5815, USA.

出版信息

RNA. 2007 Jan;13(1):5-14. doi: 10.1261/rna.259207. Epub 2006 Nov 9.

Abstract

The removal of introns from the primary transcripts of protein-coding genes is accomplished by the spliceosome, a large macromolecular complex of which small nuclear RNAs (snRNAs) are crucial components. Following the recent sequencing of the honeybee (Apis mellifera) genome, we used various computational methods, ranging from sequence similarity search to RNA secondary structure prediction, to search for putative snRNA genes (including their promoters) and to examine their pattern of conservation among 11 available insect genomes (A. mellifera, Tribolium castaneum, Bombyx mori, Anopheles gambiae, Aedes aegypti, and six Drosophila species). We identified candidates for all nine spliceosomal snRNA genes in all the analyzed genomes. All the species contain a similar number of snRNA genes, with the exception of A. aegypti, whose genome contains more U1, U2, and U5 genes, and A. mellifera, whose genome contains fewer U2 and U5 genes. We found that snRNA genes are generally more closely related to homologs within the same genus than to those in other genera. Promoter regions for all spliceosomal snRNA genes within each insect species share similar sequence motifs that are likely to correspond to the PSEA (proximal sequence element A), the binding site for snRNA activating protein complex, but these promoter elements vary in sequence among the five insect families surveyed here. In contrast to the other insect species investigated, Dipteran genomes are characterized by a rapid evolution (or loss) of components of the U12 spliceosome and a striking loss of U12-type introns.

摘要

从蛋白质编码基因的初级转录本中去除内含子是由剪接体完成的,剪接体是一种大型高分子复合物,小核RNA(snRNA)是其关键组成部分。随着蜜蜂(Apis mellifera)基因组最近测序完成,我们使用了多种计算方法,从序列相似性搜索到RNA二级结构预测,来寻找假定的snRNA基因(包括其启动子),并研究它们在11个可用昆虫基因组(意大利蜜蜂、赤拟谷盗、家蚕、冈比亚按蚊、埃及伊蚊和6种果蝇)中的保守模式。我们在所有分析的基因组中鉴定出了所有9种剪接体snRNA基因的候选基因。除埃及伊蚊(其基因组包含更多的U1、U2和U5基因)和意大利蜜蜂(其基因组包含较少的U2和U5基因)外,所有物种含有的snRNA基因数量相似。我们发现,snRNA基因通常与其同属内的同源基因比与其他属的同源基因关系更密切。每个昆虫物种内所有剪接体snRNA基因的启动子区域共享相似的序列基序,这些基序可能对应于PSEA(近端序列元件A),即snRNA激活蛋白复合物的结合位点,但这些启动子元件在本文调查的5个昆虫科中的序列有所不同。与其他被研究的昆虫物种不同,双翅目基因组的特征是U12剪接体成分的快速进化(或丢失)以及U12型内含子的显著丢失。

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