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P因子前体mRNA剪接的负调控因子PSI的体细胞特异性表达与克隆

Soma-specific expression and cloning of PSI, a negative regulator of P element pre-mRNA splicing.

作者信息

Siebel C W, Admon A, Rio D C

机构信息

Department of Molecular and Cell Biology, University of California at Berkeley 94720.

出版信息

Genes Dev. 1995 Feb 1;9(3):269-83. doi: 10.1101/gad.9.3.269.

Abstract

PSI is an RNA-binding protein involved in repressing splicing of the P element third intron in Drosophila somatic cell extracts. PSI produced in bacteria restores splicing inhibition to an extract relieved of inhibitory activity, indicating that PSI plays a direct role in somatic inhibition. Sequence analysis of cDNAs encoding PSI reveals three KH RNA-binding domains, a conserved motif also found in the yeast splicing regulator MER1. Notably, PSI is expressed highly in somatic embryonic nuclei but is undetectable in germ-line cells. In contrast, hrp48, another protein implicated in somatic inhibition, is found in the nucleus and cytoplasm of both tissues. The splicing inhibitory properties and soma-specific expression of PSI may be sufficient to explain the germ-line-specific transposition of P elements.

摘要

PSI是一种RNA结合蛋白,参与抑制果蝇体细胞提取物中P因子第三内含子的剪接。在细菌中产生的PSI可将剪接抑制恢复到去除抑制活性的提取物中,这表明PSI在体细胞抑制中起直接作用。对编码PSI的cDNA进行序列分析,发现了三个KH RNA结合结构域,这是一种在酵母剪接调节因子MER1中也存在的保守基序。值得注意的是,PSI在体细胞胚胎细胞核中高度表达,但在生殖系细胞中无法检测到。相比之下,另一种与体细胞抑制有关的蛋白hrp48在这两种组织的细胞核和细胞质中都有发现。PSI的剪接抑制特性和体细胞特异性表达可能足以解释P因子的生殖系特异性转座。

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