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在体内对定位于细胞核的RNA进行筛选。

In vivo selection of RNAs that localize in the nucleus.

作者信息

Grimm C, Lund E, Dahlberg J E

机构信息

Department of Biomolecular Chemistry, University of Wisconsin, Madison 53706, USA.

出版信息

EMBO J. 1997 Feb 17;16(4):793-806. doi: 10.1093/emboj/16.4.793.

Abstract

Nuclear localization of an RNA is affected by cis-acting elements (NLEs) that lead to nuclear import or retention or to blockage of export from the nucleus. To identify such elements, we selected and analyzed transcripts that localized in the nuclei of Xenopus laevis oocytes. The RNAs were isolated from a collection of m7G-capped RNAs in which a combinatorial library (n = 20) of sequences had been inserted. One class of selected RNAs (Sm+) had a consensus Sm binding site (AAUUUUUGG) and bound Sm proteins in the cytoplasm; these RNAs resembled small nuclear RNAs like U1 and U5 RNAs in their bi-directional nucleocytoplasmic transport and their 5'-cap hypermethylation. Another class, Sm- RNAs, contained sequences that masked the m7G-caps of the RNAs and promoted interaction with La protein. These RNAs were retained within nuclei after nuclear injection and were imported when injected into the cytoplasm. Their nuclear import and retention were independent of a 5'-cap, required an imperfect double-stranded stem near the 5' end, and depended on interaction with La protein. Import of the Sm- RNAs, while using the import pathway of proteins, was distinct from that of U6 RNA.

摘要

RNA的核定位受顺式作用元件(NLEs)影响,这些元件可导致核输入、核滞留或阻止从细胞核输出。为了鉴定此类元件,我们选择并分析了非洲爪蟾卵母细胞核中定位的转录本。这些RNA是从一组m7G加帽的RNA中分离出来的,其中插入了一个序列组合文库(n = 20)。一类选定的RNA(Sm+)具有共有Sm结合位点(AAUUUUUGG),并在细胞质中结合Sm蛋白;这些RNA在双向核质运输及其5'-帽超甲基化方面类似于U1和U5等小核RNA。另一类Sm-RNA包含掩盖RNA的m7G帽并促进与La蛋白相互作用的序列。这些RNA在核注射后保留在细胞核内,注射到细胞质中时则被输入。它们的核输入和滞留不依赖于5'-帽,需要在5'端附近有一个不完全双链茎,并依赖于与La蛋白的相互作用。Sm-RNA的输入虽然利用蛋白质的输入途径,但与U6 RNA的输入不同。

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