Detailed Information on Publication Record
2023
Human senataxin is a bona fide R-loop resolving enzyme and transcription termination factor
HAŠANOVÁ, Zdenka, Veronika KLÁPŠŤOVÁ, Odil PORRUA, Richard ŠTEFL, Marek ŠEBESTA et. al.Basic information
Original name
Human senataxin is a bona fide R-loop resolving enzyme and transcription termination factor
Authors
HAŠANOVÁ, Zdenka (703 Slovakia, belonging to the institution), Veronika KLÁPŠŤOVÁ (203 Czech Republic, belonging to the institution), Odil PORRUA, Richard ŠTEFL (203 Czech Republic, guarantor, belonging to the institution) and Marek ŠEBESTA (703 Slovakia, belonging to the institution)
Edition
Nucleic Acids Research, Oxford University Press, 2023, 0305-1048
Other information
Language
English
Type of outcome
Článek v odborném periodiku
Field of Study
10608 Biochemistry and molecular biology
Country of publisher
United Kingdom of Great Britain and Northern Ireland
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Impact factor
Impact factor: 14.900 in 2022
RIV identification code
RIV/00216224:14740/23:00132763
Organization unit
Central European Institute of Technology
UT WoS
000942750600001
Keywords in English
RNA-POLYMERASE-II; OCULOMOTOR APRAXIA TYPE-2; SACCHAROMYCES-CEREVISIAE SEN1; GENOME INSTABILITY; REPLICATION CONFLICTS; RNA/DNA HYBRIDS; PAUSE SITES; INFO-RNA; HELICASE; ATAXIA
Tags
International impact, Reviewed
Změněno: 17/10/2024 13:47, Ing. Marie Švancarová
Abstract
V originále
Prolonged pausing of the transcription machinery may lead to the formation of three-stranded nucleic acid structures, called R-loops, typically resulting from the annealing of the nascent RNA with the template DNA. Unscheduled persistence of R-loops and RNA polymerases may interfere with transcription itself and other essential processes such as DNA replication and repair. Senataxin (SETX) is a putative helicase, mutated in two neurodegenerative disorders, which has been implicated in the control of R-loop accumulation and in transcription termination. However, understanding the precise role of SETX in these processes has been precluded by the absence of a direct characterisation of SETX biochemical activities. Here, we purify and characterise the helicase domain of SETX in parallel with its yeast orthologue, Sen1. Importantly, we show that SETX is a bona fide helicase with the ability to resolve R-loops. Furthermore, SETX has retained the transcription termination activity of Sen1 but functions in a species-specific manner. Finally, subsequent characterisation of two SETX variants harbouring disease-associated mutations shed light into the effect of such mutations on SETX folding and biochemical properties. Altogether, these results broaden our understanding of SETX function in gene expression and the maintenance of genome integrity and provide clues to elucidate the molecular basis of SETX-associated neurodegenerative diseases.
Links
EF18_046/0015974, research and development project |
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GM21-10464M, research and development project |
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649030, interní kód MU |
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90127, large research infrastructures |
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