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Genome-based identification of spliceosomal proteins in the silk moth Bombyx mori

机译:基于基因组的蚕蛾剪接体蛋白鉴定

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Pre-messenger RNA splicing is a highly conserved eukaryotic cellular function that takes place by way of a large, RNA-protein assembly known as the spliceosome. In the mammalian system, nearly 300 proteins associate with uridine-rich small nuclear (sn)RNAs to form this complex. Some of these splicing factors are ubiquitously present in the spliceosome, whereas others are involved only in the processing of specific transcripts. Several proteomics analyses have delineated the proteins of the spliceosome in several species. In this study, we mine multiple sequence data sets of the silk moth Bombyx mori in an attempt to identify the entire set of known spliceosomal proteins. Five data sets were utilized, including the 3X, 6X, and Build 2.0 genomic contigs as well as the expressed sequence tag and protein libraries. While homologs for 88% of vertebrate splicing factors were delineated in the Bombyx mori genome, there appear to be several spliceosomal polypeptides absent in Bombyx mori and seven additional insect species. This apparent increase in spliceosomal complexity in vertebrates may reflect the tissue-specific and developmental stage-specific alternative pre-mRNA splicing requirements in vertebrates. Phylogenetic analyses of 15 eukaryotic taxa using the core splicing factors suggest that the essential functional units of the pre-mRNA processing machinery have remained highly conserved from yeast to humans. The Sm and LSm proteins are the most conserved, whereas proteins of the U1 small nuclear ribonucleoprotein particle are the most divergent. These data highlight both the differential conservation and relative phylogenetic signals of the essential spliceosomal components throughout evolution. © 2010 Wiley Periodicals, Inc.
机译:信使前RNA剪接是高度保守的真核细胞功能,其通过称为剪接体的大型RNA-蛋白质装配发生。在哺乳动物系统中,将近300种蛋白质与富含尿苷的小核(sn)RNA结合形成这种复合物。这些剪接因子中的一些普遍存在于剪接体中,而其他剪接因子仅涉及特定转录本的加工。几种蛋白质组学分析已经描述了几种物种中剪接体的蛋白质。在这项研究中,我们挖掘家蚕的多个序列数据集,以试图鉴定出整个已知的剪接体蛋白。利用了五个数据集,包括3X,6X和Build 2.0基因组重叠群以及表达的序列标签和蛋白质文库。虽然在家蚕基因组中描绘了88%的脊椎动物剪接因子的同源物,但家蚕似乎缺少一些剪接体多肽,另外还有7种昆虫。脊椎动物剪接体复杂性的这种明显增加可能反映了脊椎动物中组织特异性和发育阶段特异性的替代性mRNA剪接要求。使用核心剪接因子对15个真核生物类群的系统发育分析表明,从酵母到人类,mRNA加工前机械的基本功能单元一直保持高度保守。 Sm和LSm蛋白是最保守的,而U1小核糖核蛋白颗粒的蛋白则最分歧。这些数据突出了整个进化过程中必需剪接体组分的差异保守性和相对系统发生信号。 ©2010 Wiley Periodicals,Inc.

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