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中心皮质素通过动力蛋白增强其mRNA向中心体的共翻译定位。

Centrocortin potentiates co-translational localization of its mRNA to the centrosome via dynein.

作者信息

Zein-Sabatto Hala, Brockett Jovan S, Jin Li, Husbands Christian A, Lee Jina, Fang Junnan, Buehler Joseph, Bullock Simon L, Lerit Dorothy A

机构信息

Department of Cell Biology, Emory University School of Medicine, Atlanta, GA 30322.

Division of Cell Biology, MRC Laboratory of Molecular Biology, Cambridge, UK.

出版信息

bioRxiv. 2024 Aug 9:2024.08.09.607365. doi: 10.1101/2024.08.09.607365.

Abstract

Centrosomes rely upon proteins within the pericentriolar material to nucleate and organize microtubules. Several mRNAs also reside at centrosomes, although less is known about how and why they accumulate there. We previously showed that local () mRNA supports centrosome separation, microtubule organization, and viability in embryos. Here, using mRNA as a model, we examine mechanisms of centrosomal mRNA localization. We find that while the Cen N'-terminus is sufficient for protein enrichment at centrosomes, multiple domains cooperate to concentrate mRNA at this location. We further identify an N'-terminal motif within Cen that is conserved among dynein cargo adaptor proteins and test its contribution to RNA localization. Our results support a model whereby Cen protein enables the accumulation of its own mRNA to centrosomes through a mechanism requiring active translation, microtubules, and the dynein motor complex. Taken together, our data uncover the basis of translation-dependent localization of a centrosomal RNA required for mitotic integrity.

摘要

中心体依靠中心粒外周物质中的蛋白质来成核并组织微管。一些mRNA也存在于中心体中,尽管对于它们如何以及为何在那里积累了解较少。我们之前表明,局部()mRNA支持胚胎中的中心体分离、微管组织和生存能力。在这里,我们以mRNA为模型,研究中心体mRNA定位的机制。我们发现,虽然Cen N端足以使蛋白质在中心体富集,但多个结构域协同作用将mRNA集中在这个位置。我们进一步在Cen中鉴定出一个在动力蛋白货物衔接蛋白中保守的N端基序,并测试其对RNA定位的贡献。我们的结果支持一种模型,即Cen蛋白通过一种需要活跃翻译、微管和动力蛋白运动复合体的机制,使其自身mRNA在中心体积累。综上所述,我们的数据揭示了有丝分裂完整性所需的中心体RNA翻译依赖性定位的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ec06/11326273/1193188abf66/nihpp-2024.08.09.607365v1-f0001.jpg

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