Single-Molecule Quantification of Translation-Dependent Association of mRNAs with the Endoplasmic Reticulum

被引:58
作者
Voigt, Franka [1 ]
Zhang, Hui [2 ]
Cui, Xianying A. [2 ]
Triebold, Desiree [1 ,3 ]
Liu, Ai Xin [2 ]
Eglinger, Jan [1 ]
Lee, Eliza S. [2 ]
Chao, Jeffrey A. [1 ]
Palazzo, Alexander F. [2 ]
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
[2] Univ Toronto, Dept Biochem, 1 Kings Coll Circle,MSB Room 5336, Toronto, ON M5S 1A8, Canada
[3] Univ Basel, CH-4003 Basel, Switzerland
来源
CELL REPORTS | 2017年 / 21卷 / 13期
基金
加拿大自然科学与工程研究理事会; 瑞士国家科学基金会;
关键词
MEMBRANE-BOUND RIBOSOMES; UNFOLDED PROTEIN RESPONSE; GENE-EXPRESSION; IN-VIVO; MAMMALIAN-CELLS; LIVING CELLS; LIVE CELLS; TRANSLOCATION; LOCALIZATION; DYNAMICS;
D O I
10.1016/j.celrep.2017.12.008
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It is well established that mRNAs encoding secretory or membrane-bound proteins are translated on the surface of the endoplasmic reticulum (ER). The extent to which mRNAs that encode cytosolic proteins associate with the ER, however, remains controversial. To address this question, we quantified the number of cytosolic protein-encoding mRNAs that co-localize with the ER using single-molecule RNA imaging in fixed and living cells. We found that a small but significant number of mRNAs that encode cytosolic proteins associate with the ER and show that this interaction is translation dependent. Furthermore, we demonstrate that cytosolic protein-encoding transcripts can remain on the ER with dwell times consistent with multiple rounds of translation and have higher ribosome occupancies than transcripts translated in the cytosol. These results advance our understanding of the diversity and dynamics of localized translation on the ER.
引用
收藏
页码:3740 / 3753
页数:14
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