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U12 snRNA对一类次要的真核细胞核前体mRNA内含子体内剪接的需求

Requirement of U12 snRNA for in vivo splicing of a minor class of eukaryotic nuclear pre-mRNA introns.

作者信息

Hall S L, Padgett R A

机构信息

Department of Molecular Biology, Cleveland Clinic Foundation, OH 44195, USA.

出版信息

Science. 1996 Mar 22;271(5256):1716-8. doi: 10.1126/science.271.5256.1716.

Abstract

A conserved sequence element in a minor class of eukaryotic pre-messenger RNA (pre-mRNA) introns was previously proposed to base pair with a complementary sequence in the U12 small nuclear RNA (snRNA) in a manner analogous to the pairing of US snRNA with the branch site sequence of the major class of introns. Here, mutations generated in this conserved sequence element block the splicing of a member of this minor intron class in vivo. The block was relieved by coexpression of a U12 snRNA containing compensatory mutations that restore the proposed base pairing interaction. These results show that this minor class of pre-mRNA introns is a distinct class existing alongside the major class of introns in animal genomes, and these results also establish an in vivo function for U12 snRNA.

摘要

先前有人提出,真核生物前体信使RNA(pre-mRNA)小类内含子中的一个保守序列元件,会以类似于U1 snRNA与主要类内含子分支位点序列配对的方式,与U12小核RNA(snRNA)中的互补序列进行碱基配对。在此,该保守序列元件中产生的突变在体内阻断了这一小类内含子成员的剪接。通过共表达含有补偿性突变的U12 snRNA恢复了所提出的碱基配对相互作用,从而解除了阻断。这些结果表明,这类前体mRNA小类内含子是动物基因组中与主要类内含子并存的一个独特类别,这些结果还确立了U12 snRNA的体内功能。

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