Suppr超能文献

FBP2/KSRP的一个同源物与非洲爪蟾卵母细胞中的定位mRNA结合。

A homolog of FBP2/KSRP binds to localized mRNAs in Xenopus oocytes.

作者信息

Kroll Todd T, Zhao Wei-Meng, Jiang Can, Huber Paul W

机构信息

Department of Chemistry and Biochemistry, University of Notre Dame, Notre Dame, IN 46556, USA.

出版信息

Development. 2002 Dec;129(24):5609-19. doi: 10.1242/dev.00160.

Abstract

A Xenopus oocyte expression library was screened for proteins that bind to the 340-nucleotide localization element of Vg1 mRNA. Four different isolates encoded a Xenopus homolog of the human transcription factor, FUSE-binding protein 2 (FBP2). This protein has been independently identified as the splicing regulatory factor KSRP. The only significant difference between the Xenopus protein, designated VgRBP71, and KSRP is the absence of a 58 amino acid segment near the N-terminal of the former. In vivo binding assays show that VgRBP71 is associated with mRNAs localized to either the vegetal or animal hemispheres, but was not found with control mRNAs. Unlike other factors that bind to the localization element of Vg1 mRNA, VgRBP71 does not accumulate at the vegetal cortex with the mRNA; rather, it is present in the nucleus and throughout the cytoplasm at all stages of oogenesis. Cytoplasmic VgRBP71 appears to be most concentrated at the cell cortex. VgRBP71 interacts with Prrp, another protein that binds to the Vg1 localization element; this association does not require the presence of Vg1 mRNA.

摘要

利用非洲爪蟾卵母细胞表达文库筛选与Vg1 mRNA的340核苷酸定位元件结合的蛋白质。四种不同的分离株编码人类转录因子FUSE结合蛋白2(FBP2)的非洲爪蟾同源物。该蛋白已被独立鉴定为剪接调节因子KSRP。非洲爪蟾蛋白(命名为VgRBP71)与KSRP之间唯一显著的差异是前者N端附近缺少一个58个氨基酸的片段。体内结合试验表明,VgRBP71与定位于植物或动物半球的mRNA相关,但在对照mRNA中未发现。与其他结合Vg1 mRNA定位元件的因子不同,VgRBP71不会与mRNA一起在植物皮质积累;相反,它在卵子发生的所有阶段都存在于细胞核和整个细胞质中。细胞质中的VgRBP71似乎最集中在细胞皮质。VgRBP71与Prrp相互作用,Prrp是另一种与Vg1定位元件结合的蛋白质;这种结合不需要Vg1 mRNA的存在。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验