Quality control of nonstop membrane proteins at the ER membrane and in the cytosol

Shunsuke Arakawa, Kaori Yunoki, Toshiaki Izawa, Yasushi Tamura, Shuh Ichi Nishikawa, Toshiya Endo

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

Since messenger RNAs without a stop codon (nonstop mRNAs) for organelle-targeted proteins and their translation products (nonstop proteins) generate clogged translocon channels as well as stalled ribosomes, cells have mechanisms to degrade nonstop mRNAs and nonstop proteins and to clear the translocons (e.g. the Sec61 complex) by release of nonstop proteins into the organellar lumen. Here we followed the fate of nonstop endoplasmic reticulum (ER) membrane proteins with different membrane topologies in yeast to evaluate the importance of the Ltn1-dependent cytosolic degradation and the Dom34-dependent release of the nonstop membrane proteins. Ltn1-dependent degradation differed for membrane proteins with different topologies and its failure did not affect ER protein import or cell growth. On the other hand, failure in the Dom34-dependent release of the nascent polypeptide from the ribosome led to the block of the Sec61 channel and resultant inhibition of other protein import into the ER caused cell growth defects. Therefore, the nascent chain release from the translation apparatus is more instrumental in clearance of the clogged ER translocon channel and thus maintenance of normal cellular functions.

Original languageEnglish
Article number30795
JournalScientific reports
Volume6
DOIs
Publication statusPublished - 2016 Aug 2

ASJC Scopus subject areas

  • General

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