Messenger RNA delivery to mitoribosomes - hints from a bacterial toxin

被引:11
作者
Bruni, Francesco [1 ,2 ]
Proctor-Kent, Yasmin [1 ]
Lightowlers, Robert N. [3 ]
Chrzanowska-Lightowlers, Zofia M. [1 ]
机构
[1] Newcastle Univ, Inst Neurosci, Wellcome Ctr Mitochondrial Res, Newcastle Upon Tyne, Tyne & Wear, England
[2] Univ Bari Aldo Moro, Dept Biosci Biotechnol & Biopharmaceut, Via Orabona 4, I-70125 Bari, Italy
[3] Newcastle Univ, Inst Cell & Mol Biosci, Wellcome Ctr Mitochondrial Res, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国惠康基金;
关键词
LRPPRC; SLIRP; mitochondrial mRNA turnover; mitoribosome; SRL; VapC20; LARGE RIBOSOMAL-SUBUNIT; SARCIN-RICIN LOOP; CRYSTAL-STRUCTURE; EF-TU; MITOCHONDRIAL; PROTEIN; LRPPRC; GRANULES; TRANSLATION; EXPRESSION;
D O I
10.1111/febs.15342
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammalian mitochondria, messenger RNA is processed and matured from large primary transcripts in structures known as RNA granules. The identity of the factors and process transferring the matured mRNA to the mitoribosome for translation is unclear. Nascent mature transcripts are believed to associate initially with the small mitoribosomal subunit prior to recruitment of the large subunit to form the translationally active monosome. When the small subunit fails to assemble, however, the stability of mt-mRNA is only marginally affected, and under these conditions, the LRPPRC/SLIRP RNA-binding complex has been implicated in maintaining mt-mRNA stability. Here, we exploit the activity of a bacterial ribotoxin, VapC20, to show that in the absence of the large mitoribosomal subunit, mt-mRNA species are selectively lost. Further, if the small subunit is also depleted, the mt-mRNA levels are recovered. As a consequence of these data, we suggest a natural pathway for loading processed mt-mRNA onto the mitoribosome.
引用
收藏
页码:437 / 451
页数:15
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