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核糖核酸酶MRP特异性和功能的分子决定因素。

Molecular determinants of RNase MRP specificity and function.

作者信息

Smith Eric M, Ly Jimmy, Haug Sofia, Cheeseman Iain M

机构信息

Whitehead Institute for Biomedical Research, Cambridge, MA, USA.

Department of Biology, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

bioRxiv. 2025 Jan 28:2025.01.28.635360. doi: 10.1101/2025.01.28.635360.

Abstract

RNase MRP and RNase P are evolutionarily related complexes that facilitate rRNA and tRNA biogenesis, respectively. The two enzymes share nearly all protein subunits and have evolutionarily related catalytic RNAs. Notably, RNase P includes a unique subunit, Rpp21, whereas no RNase MRP-specific proteins have been found in humans, limiting molecular analyses of RNase MRP function. Here, we identify the RNase MRP-specific protein, C18orf21/RMRPP1. RMRPP1 and Rpp21 display significant structural homology, but we identify specific regions that drive interactions with their respective complexes. Additionally, we reveal that RNase MRP is required for 40S, but not 60S, ribosome biogenesis uncovering an alternative pathway for ribosome assembly. Finally, we identify Nepro as an essential rRNA processing factor that associates with the RNase MRP complex. Together, our findings elucidate the molecular determinants of RNase MRP function and underscore its critical role in ribosome biogenesis.

摘要

核糖核酸酶MRP(RNase MRP)和核糖核酸酶P(RNase P)是在进化上相关的复合物,分别促进核糖体RNA(rRNA)和转运RNA(tRNA)的生物合成。这两种酶几乎共享所有蛋白质亚基,并且具有进化上相关的催化RNA。值得注意的是,RNase P包含一个独特的亚基Rpp21,而在人类中尚未发现RNase MRP特异性蛋白,这限制了对RNase MRP功能的分子分析。在此,我们鉴定出了RNase MRP特异性蛋白C18orf21/RMRPP1。RMRPP1和Rpp21显示出显著的结构同源性,但我们确定了驱动它们与各自复合物相互作用的特定区域。此外,我们发现RNase MRP是40S核糖体生物合成所必需的,但不是60S核糖体生物合成所必需的,这揭示了核糖体组装的另一条途径。最后,我们确定Nepro是一种与RNase MRP复合物相关的必需rRNA加工因子。总之,我们的研究结果阐明了RNase MRP功能的分子决定因素,并强调了其在核糖体生物合成中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/18a2/11838342/721b5593d19a/nihpp-2025.01.28.635360v1-f0007.jpg

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