Nucleolar TFIIE plays a role in ribosomal biogenesis and performance

Author:

Phan Tamara1,Maity Pallab1,Ludwig Christina2,Streit Lisa3,Michaelis Jens3,Tsesmelis Miltiadis4,Scharffetter-Kochanek Karin1,Iben Sebastian1ORCID

Affiliation:

1. Department of Dermatology and Allergic Diseases, Ulm University, Ulm, Baden-Württemberg, 89081 Germany

2. Bavarian Center for Biomolecular Mass Spectrometry, Technical University Munich, Freising, Bavaria 85354, Germany

3. Institute of Biophysics, Ulm University, Ulm, Baden-Württemberg 89081, Germany

4. Institute of Physiological Chemistry, Ulm University, Ulm, Baden-Württemberg 89081, Germany

Abstract

Abstract Ribosome biogenesis is a highly energy-demanding process in eukaryotes which requires the concerted action of all three RNA polymerases. In RNA polymerase II transcription, the general transcription factor TFIIH is recruited by TFIIE to the initiation site of protein-coding genes. Distinct mutations in TFIIH and TFIIE give rise to the degenerative disorder trichothiodystrophy (TTD). Here, we uncovered an unexpected role of TFIIE in ribosomal RNA synthesis by RNA polymerase I. With high resolution microscopy we detected TFIIE in the nucleolus where TFIIE binds to actively transcribed rDNA. Mutations in TFIIE affects gene-occupancy of RNA polymerase I, rRNA maturation, ribosomal assembly and performance. In consequence, the elevated translational error rate with imbalanced protein synthesis and turnover results in an increase in heat-sensitive proteins. Collectively, mutations in TFIIE—due to impaired ribosomal biogenesis and translational accuracy—lead to a loss of protein homeostasis (proteostasis) which can partly explain the clinical phenotype in TTD.

Funder

German Research Foundation

DFG

Publisher

Oxford University Press (OUP)

Subject

Genetics

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