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PIWIL1和PABPC1的结构域功能分析表明它们通过减数分裂mRNA的3'-UTR在蛋白质翻译中发挥协同作用。

Domain-functional analyses of PIWIL1 and PABPC1 indicate their synergistic roles in protein translation via 3'-UTRs of meiotic mRNAs.

机构信息

School of Life Science, University of Science and Technology of China, Hefei, China.

Key Laboratory of Regenerative Biology, Guangdong Provincial Key Laboratory of Stem Cell and Regenerative Medicine, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.

出版信息

Biol Reprod. 2018 Oct 1;99(4):773-788. doi: 10.1093/biolre/ioy100.

Abstract

Translational regulation plays a central role during post-meiotic development of male germ cells. Previous studies suggested that P-element induced wimpy testis like 1 (PIWIL1), a PIWI-interacting RNA (piRNA) binding protein that is critical for sperm development, participates in the maintenance and translational regulation of post-meiotic mRNAs in haploid spermatids. However, how PIWIL1 regulates protein translation remains largely unclear. Using biochemical assays, we show here that PIWIL1 utilizes different domains to interact with post-meiotic mRNAs and Poly-A binding protein cytoplasmic 1 (PABPC1), a general protein translation regulator. PIWIL1 binds 3'-untranslated regions (3'-UTRs) of several spermiogenic mRNAs via its N-terminal domain, whereas its interactions with PABPC1 are mediated through its N- and C-terminal domains in an RNA-dependent manner. Using a heterologous cell system, we analyzed its effects on protein translation via luciferase reporter assay and sucrose gradient sedimentation. It was found that PIWIL1 augments protein translation with PABPC1 in the presence of 3'-UTRs of post-meiotic mRNAs. While both the N-terminal RNA recognition motif (RRM) domain and the central linker region of PABPC1 stimulate translation, only the PIWI Argonaute and Zwille (PAZ) domain of PIWIL1 positively affects translation of reporter mRNAs. Interestingly, the PAZ domain was found absent from polysomal fractions, in contrast to the N- and C-terminal domains of PIWIL1. Taken together, the results suggest that PIWIL1 interacts with various partners using different domains and participates in translational regulation partly through 3'-UTRs. It will be of interest to further explore how PIWIL1 elicit its versatile functions, including translational regulation of post-meiotic mRNAs through intrinsic structural changes and extrinsic signals during mouse spermiogenesis under more physiological settings.

摘要

翻译调控在雄性生殖细胞减数分裂后发育过程中起着核心作用。先前的研究表明,P元件诱导的弱精症样蛋白1(PIWIL1)是一种与PIWI相互作用RNA(piRNA)结合蛋白,对精子发育至关重要,参与单倍体精子细胞中减数分裂后mRNA的维持和翻译调控。然而,PIWIL1如何调节蛋白质翻译在很大程度上仍不清楚。通过生化分析,我们在此表明PIWIL1利用不同结构域与减数分裂后mRNA和多聚腺苷酸结合蛋白细胞质1(PABPC1,一种一般的蛋白质翻译调节因子)相互作用。PIWIL1通过其N端结构域与几种精子发生相关mRNA的3'非翻译区(3'-UTR)结合,而其与PABPC1的相互作用则通过其N端和C端结构域以RNA依赖的方式介导。利用异源细胞系统,我们通过荧光素酶报告基因检测和蔗糖梯度沉降分析了其对蛋白质翻译的影响。发现在存在减数分裂后mRNA的3'-UTR的情况下,PIWIL1与PABPC1一起增强蛋白质翻译。虽然PABPC1的N端RNA识别基序(RRM)结构域和中央连接区都能刺激翻译,但只有PIWIL1的PIWI Argonaute和Zwille(PAZ)结构域对报告基因mRNA的翻译有正向影响。有趣的是,与PIWIL1的N端和C端结构域不同,在多核糖体组分中未发现PAZ结构域。综上所述,结果表明PIWIL1利用不同结构域与各种伙伴相互作用,并部分通过3'-UTR参与翻译调控。进一步探索PIWIL1如何发挥其多种功能将是很有意义的,包括在更生理的环境下,通过小鼠精子发生过程中的内在结构变化和外在信号对减数分裂后mRNA进行翻译调控。

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