A viable hypomorphic mutation in the mitochondrial ribosome subunit, MRPS-31, exhibits mitochondrial dysfunction in C. elegans.

microPublication biology Pub Date : 2024-09-30 eCollection Date: 2024-01-01 DOI:10.17912/micropub.biology.001344
Kylie M Jozwik, James P Held, Chloe A Hecht, Maulik R Patel
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Abstract

The mitochondrial ribosome (mitoribosome) translates mitochondrial genome encoded proteins essential for cellular energy production. Given this critical role, defects in the mitoribosome can cause mitochondrial stress and manifest as multisystemic diseases. In a screen for unique activators of the mitochondrial unfolded protein response (UPR mt ) in Caenorhabditis elegans , we recovered a strain harboring a missense mutation in the gene encoding mitochondrial ribosome protein S31 ( MRPS-31 )-a component of the mitoribosome small subunit. Herein, we confirm causality of the mrps-31 allele and characterize its induction of UPR mt and impact on organismal development, providing a valuable model for further study of the mitoribosome.

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线粒体核糖体亚基MRPS-31的一个可行的低位突变在秀丽隐杆线粒体中表现出线粒体功能障碍。
线粒体核糖体(mitoribosome)能翻译线粒体基因组编码的蛋白质,这些蛋白质对细胞能量的产生至关重要。鉴于这一关键作用,线粒体核糖体的缺陷可导致线粒体应激,并表现为多系统疾病。在筛选线粒体未折叠蛋白反应(UPR mt)的独特激活剂的过程中,我们发现了一株线粒体核糖体蛋白 S31(MRPS-31)--线粒体核糖体小亚基的一个组成部分--的编码基因发生了错义突变。在这里,我们证实了mrps-31等位基因的因果关系,并描述了其诱导UPR mt和对生物体发育的影响,为进一步研究mitoribosome提供了一个有价值的模型。
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