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RhoA activation participates in rearrangement of processing bodies and release of nucleated AU-rich mRNAs

机译:RhoA激活参与加工体的重排和有核富AU的mRNA的释放

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摘要

Cytoplasmic ribonucleoprotein granules, known as processing bodies (P-bodies), contain a common set of conserved RNA-processing enzymes, and mRNAs with AU-rich elements (AREs) are delivered to P-bodies for translational silencing. Although the dynamics of P-bodies is physically linked to cytoskeletal network, it is unclear how small GTPases are involved in the P-body regulation and the ARE-mRNA metabolism. We found here that glucose depletion activates RhoA GTPase and alters the P-body dynamics in HeLa cells. These glucose-depleted effects are reproduced by the overexpression of the RhoA-subfamily GTPases and conversely abolished by the inhibition of RhoA activation. Interestingly, both RhoA activation and glucose depletion inhibit the mRNA accumulation and degradation. These findings indicate that RhoA participates in the stress-induced rearrangement of P-bodies and the release of nucleated ARE-mRNAs for their stabilization.
机译:细胞质核糖核蛋白颗粒(称为加工体(P体))包含一组共同的保守RNA加工酶,并且带有AU富集元素(ARE)的mRNA被传递到P体进行翻译沉默。尽管P体的动力学与细胞骨架网络有物理联系,但尚不清楚PTP调节和ARE-mRNA代谢中涉及多少小GTP酶。我们在这里发现葡萄糖耗竭会激活RhoA GTPase并改变HeLa细胞中的P体动力学。通过RhoA亚家族GTPase的过表达来再现这些葡萄糖耗尽的效应,相反,通过抑制RhoA激活而消除这些葡萄糖耗尽的效应。有趣的是,RhoA激活和葡萄糖消耗均抑制mRNA的积累和降解。这些发现表明,RhoA参与了应力诱导的P体重排和有核ARE-mRNA的释放,以使其稳定。

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