NEMF-mediated CAT tailing facilitates translocation-associated quality control

Ribosome stalling during co-translational translocation at the ER causes translocon clogging and impairs ER protein biogenesis. Mammalian cells resolve translocon clogging via a poorly characterized translocation-associated quality control (TAQC) process. Here, we combine a genome-wide CRISPR screen with live-cell imaging to dissect the molecular linchpin of TAQC. We show that TAQC substrates translated from mRNAs bearing a ribosome-stalling poly(A) sequence are degraded by lysosomes and the proteasome. By contrast, the degradation of defective nascent chains encoded by nonstop (NS) mRNAs involves an unconventional ER-associated protein degradation (ERAD) mechanism depending on ER-to-Golgi trafficking, KDEL-mediated substrate retrieval at the Golgi, and a tRNA-binding factor NEMF that appends an aggregation-prone carboxyl tail to stalled NS nascent chains. We propose that NEMF-mediated CAT tailing targets a subset of TAQC substrates via Golgi retrieval for ERAD, safeguarding ER homeostasis.

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Publication Details

Journal
The Journal of Cell Biology
Published
2025-04-21
DOI
https://doi.org/10.1083/jcb.202408199
Citations
2
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
1.61

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article

NEMF-mediated CAT tailing facilitates translocation-associated quality control

Yue Xu, Clinton Yu, Yihong Ye, Layla Saidi et al.
2 citations
The Journal of Cell Biology
RNA and protein synthesis mechanisms
1.61
article

NEMF-mediated CAT tailing facilitates translocation-associated quality control

Yue Xu, Clinton Yu, Yihong Ye, Layla Saidi, Lihui Wang, Lan Huang, Wang Xiaorong, Sijung Yun, Amanda Ennis
article en
2 citations

Abstract

Ribosome stalling during co-translational translocation at the ER causes translocon clogging and impairs ER protein biogenesis. Mammalian cells resolve translocon clogging via a poorly characterized translocation-associated quality control (TAQC) process. Here, we combine a genome-wide CRISPR screen with live-cell imaging to dissect the molecular linchpin of TAQC. We show that TAQC substrates translated from mRNAs bearing a ribosome-stalling poly(A) sequence are degraded by lysosomes and the proteasome. By contrast, the degradation of defective nascent chains encoded by nonstop (NS) mRNAs involves an unconventional ER-associated protein degradation (ERAD) mechanism depending on ER-to-Golgi trafficking, KDEL-mediated substrate retrieval at the Golgi, and a tRNA-binding factor NEMF that appends an aggregation-prone carboxyl tail to stalled NS nascent chains. We propose that NEMF-mediated CAT tailing targets a subset of TAQC substrates via Golgi retrieval for ERAD, safeguarding ER homeostasis.

The Journal of Cell BiologyVol. 224(6)
National Institutes of Health (US), University of California, Irvine (US), National Institute of Diabetes and Digestive and Kidney Diseases (US)
National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases
Openalex Percentile: Top 18%
RNA and protein synthesis mechanisms
1.61
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NEMF-mediated CAT tailing facilitates translocation-associated quality control — Yue Xu, Clinton Yu, et al. · The Journal of Cell Biology (2025) | TGRS Research Map | TGRS