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扁形虫中剪接前导RNA令人惊讶的多样性和分布

Surprising diversity and distribution of spliced leader RNAs in flatworms.

作者信息

Davis R E

机构信息

Department of Biological Sciences, Fordham University, Bronx, NY 10458, USA.

出版信息

Mol Biochem Parasitol. 1997 Jul;87(1):29-48. doi: 10.1016/s0166-6851(97)00040-6.

Abstract

Trans-splicing generates the mature 5' ends of certain mRNAs through the addition of a small spliced leader (SL) exon to pre-mRNAs. To search for novel flatworm spliced leaders, degenerate oligonucleotides and 5' RACE [corrected was used to isolate and characterize the 5' terminal sequences of enolase mRNAs in diverse flatworms. Several new spliced leaders and their SL RNA genes were identified, characterized, and compared. All parasitic trematodes examined trans-splice enolase. A primitive polyclad turbellarian, Stylochus zebra, also contains a trans-spliced enolase mRNA. The S. zebra SL is the longest SL yet identified, 51 nucleotides. Comparison of flatworm SLs indicates that they vary significantly in sequence and length. This suggests that neither spliced leader exon sequence nor size is likely to be essential for trans-splicing in flatworms. Flatworm SL RNAs have unusual Sm binding sites with characteristics distinct from other known flatworm snRNA Sm binding sites. Predicted flatworm SL RNA secondary structures show variation exhibiting 2-4 stem loops. Although limited in sequence similarity, phylogenetically conserved regions within the diverse flatworm SL RNAs suggest that they are likely to be derived from a common ancestor and provide information on potentially important SL RNA elements. The identification of a SL in a primitive flatworm suggests that trans-splicing may have been an ancestral feature in the phylum. Representative species of other early and more recent clades within the phylum, however, do not trans-splice enolase, nor do they or representatives of several other flatworm groups, have an SL RNA with a phylogenetically conserved region identified in the current study.

摘要

反式剪接通过向前体mRNA添加一个小的剪接前导(SL)外显子来产生某些mRNA的成熟5'末端。为了寻找新的扁虫剪接前导序列,使用简并寡核苷酸和5' RACE [已校正]来分离和表征不同扁虫中烯醇化酶mRNA的5'末端序列。鉴定、表征并比较了几种新的剪接前导序列及其SL RNA基因。所有检测的寄生吸虫都对烯醇化酶进行反式剪接。一种原始的多肠目涡虫,斑马纹Stylochus,也含有反式剪接的烯醇化酶mRNA。斑马纹Stylochus的SL是迄今鉴定出的最长的SL,有51个核苷酸。扁虫SL的比较表明它们在序列和长度上有显著差异。这表明剪接前导外显子序列和大小对于扁虫的反式剪接可能都不是必需的。扁虫SL RNA具有不寻常的Sm结合位点,其特征与其他已知的扁虫snRNA Sm结合位点不同。预测的扁虫SL RNA二级结构显示出具有2 - 4个茎环的变异。尽管序列相似性有限,但不同扁虫SL RNA中的系统发育保守区域表明它们可能源自共同祖先,并提供了关于潜在重要的SL RNA元件的信息。在一种原始扁虫中鉴定出SL表明反式剪接可能是该门的一个祖先特征。然而,该门内其他早期和近期类群的代表性物种既不反式剪接烯醇化酶,它们或其他几个扁虫类群的代表也没有在本研究中鉴定出的具有系统发育保守区域的SL RNA。

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