| Literature DB >> 34203326 |
Mingyue Qiang1, Fatima Khalid1, Tamara Phan1, Christina Ludwig2, Karin Scharffetter-Kochanek1, Sebastian Iben1.
Abstract
Cockayne syndrome (CS) is a developmental disorder with symptoms that are typical for the aging body, including subcutaneous fat loss, alopecia, and cataracts. Here, we show that in the cells of CS patients, RNA polymerase I transcription and the processing of the pre-rRNA are disturbed, leading to an accumulation of the 18S-E intermediate. The mature 18S rRNA level is reduced, and isolated ribosomes lack specific ribosomal proteins of the small 40S subunit. Ribosomal proteins are susceptible to unfolding and the CS cell proteome is heat-sensitive, indicating misfolded proteins and an error-prone translation process in CS cells. Pharmaceutical chaperones restored impaired cellular proliferation. Therefore, we provide evidence for severe protein synthesis malfunction, which together with a loss of proteostasis constitutes the underlying pathophysiology in CS.Entities:
Keywords: Cockayne syndrome; RNA polymerase I; loss of proteostasis; ribosome; translational fidelity
Year: 2021 PMID: 34203326 DOI: 10.3390/cells10071616
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600