Cockayne syndrome mutation in XPG activate the integrated stress response

Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are diseases provoked by mutations in multifunctional proteins that are involved in DNA repair. DNA-repair deficiency explains the high cancer incidence of XP, whereas cancer-free CS, characterized by growth retardation, neurological degeneration, and premature aging does not present as a classical DNA-repair deficiency disorder. Here, we compared a severe combined XP/CS case provoked by XPG-mutation with an XP "only" patient cell line caused by mutation in the same XPG gene to carve out the pathogenic cellular disturbances that provoke CS. We identified RNA polymerase I transcription and rRNA maturation defects, a highly phosphorylated eukaryotic initiation factor 2 alpha (eIF2alpha), and a shift from cap- to internal ribosomal entry site (IRES) translation, indicating an activated integrated stress response in CS. Disturbances in ribosomal biogenesis and translational control might thus contribute to the development of CS.

Authors

Institutions

Publication Details

Journal
Human Genetics
Published
2026-01-21
DOI
https://doi.org/10.1007/s00439-025-02804-3
Primary Topic
DNA Repair Mechanisms
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Cockayne syndrome mutation in XPG activate the integrated stress response

Zhouli Cao, Gaojie Zhu, Karin Scharffetter‐­Kochanek, Steffen Emmert et al.
Human Genetics
DNA Repair Mechanisms
article

Cockayne syndrome mutation in XPG activate the integrated stress response

Zhouli Cao, Gaojie Zhu, Karin Scharffetter‐­Kochanek, Steffen Emmert, Çagatay Güneş, Sebastian Iben, D. Zhang, Gregoire Najjar, Max Hartmann
article en

Abstract

Xeroderma pigmentosum (XP) and Cockayne syndrome (CS) are diseases provoked by mutations in multifunctional proteins that are involved in DNA repair. DNA-repair deficiency explains the high cancer incidence of XP, whereas cancer-free CS, characterized by growth retardation, neurological degeneration, and premature aging does not present as a classical DNA-repair deficiency disorder. Here, we compared a severe combined XP/CS case provoked by XPG-mutation with an XP "only" patient cell line caused by mutation in the same XPG gene to carve out the pathogenic cellular disturbances that provoke CS. We identified RNA polymerase I transcription and rRNA maturation defects, a highly phosphorylated eukaryotic initiation factor 2 alpha (eIF2alpha), and a shift from cap- to internal ribosomal entry site (IRES) translation, indicating an activated integrated stress response in CS. Disturbances in ribosomal biogenesis and translational control might thus contribute to the development of CS.

Human GeneticsVol. 145(1)
Universität Ulm (DE), University Hospital Ulm (DE), Technische Hochschule Ulm (DE), University of Rostock (DE)
Deutsche Forschungsgemeinschaft, Universität Ulm
Good health and well-being
Openalex Percentile: Top 82%
DNA Repair Mechanisms
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.