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酿酒酵母核糖体蛋白Rpl3p在核糖体合成中的功能分析

Functional analysis of Saccharomyces cerevisiae ribosomal protein Rpl3p in ribosome synthesis.

作者信息

Rosado Iván V, Kressler Dieter, de la Cruz Jesús

机构信息

Departamento de Genética, Universidad de Sevilla, Sevilla, Spain.

出版信息

Nucleic Acids Res. 2007;35(12):4203-13. doi: 10.1093/nar/gkm388. Epub 2007 Jun 13.

Abstract

Ribosome synthesis in eukaryotes requires a multitude of trans-acting factors. These factors act at many steps as the pre-ribosomal particles travel from the nucleolus to the cytoplasm. In contrast to the well-studied trans-acting factors, little is known about the contribution of the ribosomal proteins to ribosome biogenesis. Herein, we have analysed the role of ribosomal protein Rpl3p in 60S ribosomal subunit biogenesis. In vivo depletion of Rpl3p results in a deficit in 60S ribosomal subunits and the appearance of half-mer polysomes. This phenotype is likely due to the instability of early and intermediate pre-ribosomal particles, as evidenced by the low steady-state levels of 27SA(3), 27SB(S) and 7S(L/S) precursors. Furthermore, depletion of Rpl3p impairs the nucleocytoplasmic export of pre-60S ribosomal particles. Interestingly, flow cytometry analysis indicates that Rpl3p-depleted cells arrest in the G1 phase. Altogether, we suggest that upon depletion of Rpl3p, early assembly of 60S ribosomal subunits is aborted and subsequent steps during their maturation and export prevented.

摘要

真核生物中的核糖体合成需要多种反式作用因子。当核糖体前体颗粒从核仁运输到细胞质时,这些因子在多个步骤发挥作用。与研究充分的反式作用因子不同,人们对核糖体蛋白在核糖体生物发生中的作用了解甚少。在此,我们分析了核糖体蛋白Rpl3p在60S核糖体亚基生物发生中的作用。体内Rpl3p的缺失导致60S核糖体亚基数量不足以及出现半聚核糖体。这种表型可能是由于早期和中间核糖体前体颗粒的不稳定性,27SA(3)、27SB(S)和7S(L/S)前体的低稳态水平证明了这一点。此外,Rpl3p的缺失会损害60S核糖体前体颗粒的核质输出。有趣的是,流式细胞术分析表明,Rpl3p缺失的细胞停滞在G1期。总之,我们认为,Rpl3p缺失后,60S核糖体亚基的早期组装失败,随后其成熟和输出过程中的后续步骤也受到阻碍。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a46/1919493/137e89b4fdef/gkm388f1.jpg

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