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剪接体内U5小核核糖核蛋白(snRNP)的p220可识别位于5'剪接位点的典型GU二核苷酸。

The canonical GU dinucleotide at the 5' splice site is recognized by p220 of the U5 snRNP within the spliceosome.

作者信息

Reyes J L, Kois P, Konforti B B, Konarska M M

机构信息

Rockefeller University, New York, New York 10021, USA.

出版信息

RNA. 1996 Mar;2(3):213-25.

Abstract

Specific recognition of the 5' splice site (5'SS) by the spliceosome components was studied using a simple in vitro system in which a short 5'SS RNA oligonucleotide specifically induces the assembly of snRNP particles into spliceosome-like complexes and actively participates in a trans-splicing reaction. Short-range cross-liking demonstrates that a U5 snRNP protein component, p220 (the human analogue of the yeast Prp8) specifically interacts with the invariant GU dinucleotide at the 5' end of the intron. The GU:p220 interaction can be detected in the functional splicing complex B. Although p220 has been known to contact several nucleotides around the 5' splice junction, the p220:GU dinucleotide interaction described here is remarkably specific. Consistent with the high conservation of the GU, even minor modifications of this element affect recognition of the 5'SS RNA by p220. Substitution of uridine at the GU with base analogues containing a large methyl or iodo group, but not a smaller flouro group at base position 5, interferes with association of 5'SS RNA with snRNP complexes and their functional participation in splicing.

摘要

利用一个简单的体外系统研究了剪接体成分对5'剪接位点(5'SS)的特异性识别,在该系统中,一个短的5'SS RNA寡核苷酸特异性诱导snRNP颗粒组装成剪接体样复合物,并积极参与反式剪接反应。短程交联表明,U5 snRNP蛋白成分p220(酵母Prp8的人类类似物)与内含子5'端的不变GU二核苷酸特异性相互作用。GU:p220相互作用可在功能性剪接复合物B中检测到。尽管已知p220与5'剪接连接处周围的几个核苷酸接触,但此处描述的p220:GU二核苷酸相互作用具有显著特异性。与GU的高度保守性一致,该元件的即使微小修饰也会影响p220对5'SS RNA的识别。将GU处的尿苷替换为在碱基位置5含有大甲基或碘基团而非较小氟基团的碱基类似物,会干扰5'SS RNA与snRNP复合物的结合及其在剪接中的功能参与。

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