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多毛短膜虫中多种mRNA循环序列元件结合蛋白的存在。

Presence of multiple mRNA cycling sequence element-binding proteins in Crithidia fasciculata.

作者信息

Mittra Bidyottam, Sinha Krishna M, Hines Jane C, Ray Dan S

机构信息

Molecular Biology Institute and Department of Microbiology, Immunology and Molecular Genetics, University of California, Los Angeles, California 90095, USA.

出版信息

J Biol Chem. 2003 Jul 18;278(29):26564-71. doi: 10.1074/jbc.M304322200. Epub 2003 May 3.

Abstract

A consensus sequence present in the 5'- or 3'-untranslated regions of several Crithidia fasciculata messenger RNAs encoding proteins involved in DNA metabolism has been shown to be necessary for the periodic accumulation of these mRNAs during the cell cycle. A protein complex termed cycling sequence-binding protein (CSBP) has two subunits, CSBPA and CSBPB, and binds the consensus sequence with high specificity. The binding activity of CSBP was shown to vary during the cell cycle in parallel with the levels of putative target mRNAs. Although disruption of the CSBPA gene resulted in loss of both CSBPA and CSBPB, the putative target message levels still continued to vary during the cell cycle. The presence of an additional and distinct binding activity was revealed in these CSBPA null mutant cells. This activity, termed CSBP II, was also expressed in wild-type Crithidia cells. CSBP II has higher binding specificity for the cycling sequence element than the earlier described CSBP complex. Three polypeptides associated with purified CSBP II show specific binding to the cycling sequence. These proteins may represent a family of sequence-specific RNA-binding proteins involved in post-transcriptional regulation.

摘要

在几种编码参与DNA代谢的蛋白质的克氏锥虫信使核糖核酸(mRNA)的5'-或3'-非翻译区中存在的一个共有序列,已被证明对于这些mRNA在细胞周期中的周期性积累是必需的。一种称为循环序列结合蛋白(CSBP)的蛋白质复合物有两个亚基,即CSBPA和CSBPB,并以高特异性结合该共有序列。CSBP的结合活性在细胞周期中与假定的靶mRNA水平平行变化。虽然CSBPA基因的破坏导致CSBPA和CSBPB都缺失,但假定的靶信使水平在细胞周期中仍继续变化。在这些CSBPA基因敲除突变细胞中发现了另一种不同的结合活性。这种活性称为CSBP II,在野生型克氏锥虫细胞中也有表达。与早期描述的CSBP复合物相比,CSBP II对循环序列元件具有更高的结合特异性。与纯化的CSBP II相关的三种多肽显示出与循环序列的特异性结合。这些蛋白质可能代表参与转录后调控的序列特异性RNA结合蛋白家族。

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