Department of Molecular Genetics, Ohio State University, Columbus, OH 43235, USA.
Center for RNA Biology, Ohio State University, Columbus, OH 43235, USA.
Nucleic Acids Res. 2022 Sep 23;50(17):10140-10152. doi: 10.1093/nar/gkac754.
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.
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。