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PUF-8 和 TCER-1 对于线虫生殖细胞中多种 mRNA 的正常水平是必需的。

PUF-8 and TCER-1 are essential for normal levels of multiple mRNAs in the C. elegans germline.

机构信息

Department of Biological Sciences and Bioengineering, Indian Institute of Technology, Kanpur 208016, India.

出版信息

Development. 2013 Mar;140(6):1312-20. doi: 10.1242/dev.087833.

Abstract

PUF family proteins are well-conserved regulators of cell proliferation in different developmental processes. They regulate target mRNAs by promoting degradation or by influencing translation through interaction with the translation initiation machinery. Here we show that Caenorhabditis elegans PUF-8 functions redundantly with the nuclear protein TCER-1 in the post-transcriptional maintenance of at least six germline mRNAs. The levels of spliced mRNAs in the puf-8(-) tcer-1(-) double mutant are only 10-30% of the wild type, whereas the unspliced forms increase by ∼2- to 3-fold compared with the wild type. These two proteins colocalise at the inner nuclear periphery, and their absence leads to reduced germ cell proliferation and to sterility. A yeast two-hybrid screen of 31 components of the nuclear pore complex and mRNA processing machineries identified seven proteins involved in mRNA export as potential partners of PUF-8. One of these, the nuclear cap-binding protein NCBP-2, colocalises with PUF-8 in the nucleus. A 50 amino acid N-terminal domain of PUF-8 is essential for interaction with NCBP-2 and for PUF-8 to function redundantly with TCER-1. These results reveal two important unexpected aspects of PUF proteins: that, in addition to the C-terminal PUF domain, the N-terminal domain is crucial for PUF function, and that PUF proteins have a novel role in mRNA maintenance. We propose that PUF proteins, in addition to their known cytoplasmic roles, participate in nuclear processing and/or export of mRNAs.

摘要

PUF 家族蛋白是不同发育过程中细胞增殖的高度保守调节因子。它们通过与翻译起始机制相互作用,促进靶 mRNA 的降解或影响翻译,从而调节靶 mRNA。在这里,我们表明,秀丽隐杆线虫 PUF-8 与核蛋白 TCER-1 冗余地发挥作用,在后转录水平维持至少六种生殖系 mRNA。puf-8(-) tcer-1(-) 双突变体中剪接 mRNA 的水平仅为野生型的 10-30%,而未剪接形式比野生型增加了约 2-3 倍。这两种蛋白在核内周缘共定位,它们的缺失导致生殖细胞增殖减少和不育。核孔复合体和 mRNA 处理机器的 31 个成分的酵母双杂交筛选鉴定出 7 种参与 mRNA 输出的蛋白作为 PUF-8 的潜在伴侣。其中一种是核帽结合蛋白 NCBP-2,它与 PUF-8 在核内共定位。PUF-8 的 50 个氨基酸 N 端结构域对于与 NCBP-2 的相互作用以及 PUF-8 与 TCER-1 的冗余功能是必需的。这些结果揭示了 PUF 蛋白的两个重要的意外方面:除了 C 端 PUF 结构域外,N 端结构域对于 PUF 功能至关重要,以及 PUF 蛋白在 mRNA 维持方面具有新的作用。我们提出,除了已知的细胞质作用外,PUF 蛋白还参与 mRNA 的核处理和/或输出。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca57/3585663/d06800c6c120/DEV087833F1.jpg

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