Nuclear mRNA metabolism drives selective basket assembly on a subset of nuclear pore complexes in budding yeast

被引:18
|
作者
Bensidoun, Pierre [1 ,2 ]
Reiter, Taylor [3 ]
Montpetit, Ben [3 ]
Zenklusen, Daniel [2 ]
Oeffinger, Marlene [1 ,2 ,4 ]
机构
[1] Inst Rech Clin Montreal IRCM, Montreal, PQ, Canada
[2] Univ Montreal, Dept Biochim & Med Mol, Montreal, PQ, Canada
[3] Univ Calif Davis, Dept Viticulture & Enol, Davis, CA USA
[4] McGill Univ, Div Expt Med, Montreal, PQ, Canada
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
GLOBAL ANALYSIS; PROTEIN; EXPORT; RETENTION; LOCALIZATION; DYNAMICS; ASSOCIATION; TRANSPORT; TPR; ARCHITECTURE;
D O I
10.1016/j.molcel.2022.09.019
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
To determine which transcripts should reach the cytoplasm for translation, eukaryotic cells have established mechanisms to regulate selective mRNA export through the nuclear pore complex (NPC). The nuclear basket, a substructure of the NPC protruding into the nucleoplasm, is thought to function as a stable platform where mRNA-protein complexes (mRNPs) are rearranged and undergo quality control prior to export, ensuring that only mature mRNAs reach the cytoplasm. Here, we use proteomic, genetic, live-cell, and single-molecule res-olution microscopy approaches in budding yeast to demonstrate that basket formation is dependent on RNA polymerase II transcription and subsequent mRNP processing. We further show that while all NPCs can bind Mlp1, baskets assemble only on a subset of nucleoplasmic NPCs, and these basket-containing NPCs asso-ciate a distinct protein and RNA interactome. Taken together, our data point toward NPC heterogeneity and an RNA-dependent mechanism for functionalization of NPCs in budding yeast through nuclear basket as-sembly.
引用
收藏
页码:3856 / +
页数:23
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