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翻译因子 mRNA 颗粒将蛋白质合成能力导向极化生长的区域。

Translation factor mRNA granules direct protein synthetic capacity to regions of polarized growth.

机构信息

Division of Molecular and Cellular Function, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.

Universidad de Buenos Aires, Instituto de Química Biológica de la Facultad de Ciencias Exactas y Naturales-Consejo Nacional de Investigaciones Científicas y Técnicas, Buenos Aires, Argentina.

出版信息

J Cell Biol. 2019 May 6;218(5):1564-1581. doi: 10.1083/jcb.201704019. Epub 2019 Mar 15.

Abstract

mRNA localization serves key functions in localized protein production, making it critical that the translation machinery itself is present at these locations. Here we show that translation factor mRNAs are localized to distinct granules within yeast cells. In contrast to many messenger RNP granules, such as processing bodies and stress granules, which contain translationally repressed mRNAs, these granules harbor translated mRNAs under active growth conditions. The granules require Pab1p for their integrity and are inherited by developing daughter cells in a She2p/She3p-dependent manner. These results point to a model where roughly half the mRNA for certain translation factors is specifically directed in granules or translation factories toward the tip of the developing daughter cell, where protein synthesis is most heavily required, which has particular implications for filamentous forms of growth. Such a feedforward mechanism would ensure adequate provision of the translation machinery where it is to be needed most over the coming growth cycle.

摘要

mRNA 定位在局部蛋白质产生中起着关键作用,因此翻译机制本身必须存在于这些位置。在这里,我们表明翻译因子 mRNA 定位于酵母细胞内的不同颗粒中。与许多信使 RNP 颗粒(如加工体和应激颗粒)不同,这些颗粒包含翻译受抑制的 mRNA,在活跃生长条件下,这些颗粒中含有翻译的 mRNA。这些颗粒需要 Pab1p 才能保持完整,并以 She2p/She3p 依赖的方式遗传给发育中的子细胞。这些结果表明了一种模型,即某些翻译因子的 mRNA 大约有一半被特异性地导向颗粒或翻译工厂,朝向发育中子细胞的尖端,那里是蛋白质合成需求最旺盛的地方,这对丝状生长形式具有特殊意义。这种前馈机制将确保在未来的生长周期中,在最需要的地方提供足够的翻译机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4c8/6504908/1fa54123eb29/JCB_201704019_Fig1.jpg

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