Suppr超能文献

酿酒酵母中三种 tRNA 核输出蛋白:平行途径、偏好和精确性。

Three tRNA nuclear exporters in S. cerevisiae: parallel pathways, preferences, and precision.

机构信息

Department of Molecular Genetics, Ohio State University, Columbus, OH 43235, USA.

Center for RNA Biology, Ohio State University, Columbus, OH 43235, USA.

出版信息

Nucleic Acids Res. 2022 Sep 23;50(17):10140-10152. doi: 10.1093/nar/gkac754.

Abstract

tRNAs that are transcribed in the nucleus are exported to the cytoplasm to perform their iterative essential function in translation. However, the complex set of tRNA post-transcriptional processing and subcellular trafficking steps are not completely understood. In particular, proteins involved in tRNA nuclear export remain unknown since the canonical tRNA nuclear exportin, Los1/Exportin-t, is unessential in all tested organisms. We previously reported that budding yeast Mex67-Mtr2, a mRNA nuclear exporter, co-functions with Los1 in tRNA nuclear export. Here we employed in vivo co-purification of tRNAs with endogenously expressed nuclear exporters to document that Crm1 also is a bona fide tRNA nuclear exporter. We document that Los1, Mex67-Mtr2 and Crm1 possess individual tRNA preferences for forming nuclear export complexes with members of the 10 families of intron-containing pre-tRNAs. Remarkably, Mex67-Mtr2, but not Los1 or Crm1, is error-prone, delivering tRNAs to the cytoplasm prior to 5' leader removal. tRNA retrograde nuclear import functions to monitor the aberrant leader-containing spliced tRNAs, returning them to the nucleus where they are degraded by 3' to 5' exonucleases. Overall, our work identifies a new tRNA nuclear exporter, uncovers exporter preferences for specific tRNA families, and documents contribution of tRNA nuclear import to tRNA quality control.

摘要

在细胞核中转录的 tRNA 被输出到细胞质中,以在翻译中执行其迭代的基本功能。然而,tRNA 转录后加工和亚细胞运输步骤的复杂集合还不完全清楚。特别是,由于在所有测试的生物体中,经典的 tRNA 核输出蛋白 Los1/Exportin-t 都是非必需的,因此参与 tRNA 核输出的蛋白质仍然未知。我们之前报道过,芽殖酵母 Mex67-Mtr2,一种 mRNA 核输出蛋白,与 Los1 共同作用于 tRNA 的核输出。在这里,我们采用体内共纯化与内源性表达的核输出蛋白的 tRNA,证明 Crm1 也是一种真正的 tRNA 核输出蛋白。我们证明,Los1、Mex67-Mtr2 和 Crm1 分别具有与包含内含子的前 tRNA 的 10 个家族成员形成核输出复合物的 tRNA 偏好性。值得注意的是,Mex67-Mtr2,但不是 Los1 或 Crm1,是易错的,在 5' 前导去除之前将 tRNA 递送到细胞质中。tRNA 逆行核输入功能可监测含有异常前导的拼接 tRNA,将其返回到细胞核,在那里它们被 3' 到 5' 的外切核酸酶降解。总的来说,我们的工作确定了一种新的 tRNA 核输出蛋白,揭示了输出蛋白对特定 tRNA 家族的偏好,并记录了 tRNA 核输入对 tRNA 质量控制的贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7e0f/9508810/2e5e4c3f7287/gkac754fig1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验