Suppr超能文献

驱动蛋白 KIF18A 是一种新型的 PUM 调节靶标,可促进人类精原细胞瘤系的有丝分裂进程和存活。

Kinesin KIF18A is a novel PUM-regulated target promoting mitotic progression and survival of a human male germ cell line.

机构信息

Institute of Human Genetics, Polish Academy of Sciences, Strzeszynska 32, 60-479 Poznan, Poland

Institute of Bioorganic Chemistry, Polish Academy of Sciences, Noskowskiego 12/14, 61-704 Poznan, Poland.

出版信息

J Cell Sci. 2020 Apr 6;133(7):jcs240986. doi: 10.1242/jcs.240986.

Abstract

Regulation of proliferation, apoptosis and cell cycle is crucial for the physiology of germ cells. Their malfunction contributes to infertility and germ cell tumours. The kinesin KIF18A is an important regulator of those processes in animal germ cells. Post-transcriptional regulation of KIF18A has not been extensively explored. Owing to the presence of PUM-binding elements (PBEs), mRNA is a potential target of PUM proteins, where PUM refers to Pumilio proteins, RNA-binding proteins that act in post-transcriptional gene regulation. We conducted RNA co-immunoprecipitation combined with RT-qPCR, as well as luciferase reporter assays, by applying an appropriate luciferase construct encoding wild-type 3'-UTR, upon PUM overexpression or knockdown in TCam-2 cells, representing human male germ cells. We found that KIF18A is repressed by PUM1 and PUM2. To study how this regulation influences KIF18A function, an MTS proliferation assay, and apoptosis and cell cycle analysis using flow cytometry, was performed upon mRNA siRNA knockdown. KIF18A significantly influences proliferation, apoptosis and the cell cycle, with its effects being opposite to PUM effects. Repression by PUM proteins might represent one of mechanisms influencing KIF18A level in controlling proliferation, cell cycle and apoptosis in TCam-2 cells.

摘要

调控增殖、凋亡和细胞周期对于生殖细胞的生理功能至关重要。其功能障碍会导致不孕和生殖细胞瘤。驱动蛋白 KIF18A 是动物生殖细胞中这些过程的重要调节因子。KIF18A 的转录后调控尚未得到广泛探索。由于存在 PUM 结合元件(PBEs),mRNA 可能是 PUM 蛋白的潜在靶标,PUM 是指 Pumilio 蛋白,这是一种在转录后基因调控中起作用的 RNA 结合蛋白。我们通过在 TCam-2 细胞中转染适当的编码野生型 3'UTR 的荧光素酶报告基因构建体,进行了 RNA 免疫共沉淀结合 RT-qPCR 以及荧光素酶报告基因测定,在这些细胞中转染 PUM1 和 PUM2 过表达或敲低质粒。我们发现 KIF18A 受到 PUM1 和 PUM2 的抑制。为了研究这种调控如何影响 KIF18A 的功能,我们在 TCam-2 细胞中转染 KIF18A mRNA siRNA 后进行了 MTS 增殖测定、流式细胞术分析凋亡和细胞周期。KIF18A 显著影响增殖、凋亡和细胞周期,其作用与 PUM 的作用相反。PUM 蛋白的抑制可能是影响 KIF18A 水平以控制 TCam-2 细胞增殖、细胞周期和凋亡的机制之一。

相似文献

7
Essential requirement of mammalian Pumilio family in embryonic development.哺乳动物 pumilio 家族在胚胎发育中的基本要求。
Mol Biol Cell. 2018 Nov 26;29(24):2922-2932. doi: 10.1091/mbc.E18-06-0369. Epub 2018 Sep 26.

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