BOLOGNA, Serena, Veronika ALTMANNOVÁ, Emanuele VALTORTA, Christiane KOENIG, Prisca LIBERALI, Christian GENTILI, Dorothea ANRATHER, Gustav AMMERER, Lucas PELKMANS, Lumír KREJČÍ and Stefano FERRARI. Sumoylation regulates EXO1 stability and processing of DNA damage. Cell Cycle. Philadelohia: TAYLOR & FRANCIS INC, 2015, vol. 14, No 15, p. 2439-2450. ISSN 1538-4101. Available from: https://dx.doi.org/10.1080/15384101.2015.1060381.
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Basic information
Original name Sumoylation regulates EXO1 stability and processing of DNA damage
Authors BOLOGNA, Serena (756 Switzerland), Veronika ALTMANNOVÁ (203 Czech Republic, belonging to the institution), Emanuele VALTORTA (380 Italy), Christiane KOENIG (756 Switzerland), Prisca LIBERALI (756 Switzerland), Christian GENTILI (756 Switzerland), Dorothea ANRATHER (40 Austria), Gustav AMMERER (40 Austria), Lucas PELKMANS (756 Switzerland), Lumír KREJČÍ (203 Czech Republic, guarantor, belonging to the institution) and Stefano FERRARI (756 Switzerland).
Edition Cell Cycle, Philadelohia, TAYLOR & FRANCIS INC, 2015, 1538-4101.
Other information
Original language English
Type of outcome Article in a journal
Field of Study Genetics and molecular biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.952
RIV identification code RIV/00216224:14110/15:00081061
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1080/15384101.2015.1060381
UT WoS 000359768900015
Keywords in English chromosome aberrations; DNA resection; exonuclease-1; sumoylation; ubiquitylation
Tags EL OK, podil
Tags International impact, Reviewed
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 29/9/2015 13:06.
Abstract
DNA double-strand break repair by the error-free pathway of homologous recombination (HR) requires the concerted action of several factors. Among these, EXO1 and DNA2/BLM are responsible for the extensive resection of DNA ends to produce 3'-overhangs, which are essential intermediates for downstream steps of HR. Here we show that EXO1 is a SUMO target and that sumoylation affects EXO1 ubiquitylation and protein stability. We identify an UBC9-PIAS1/PIAS4-dependent mechanism controlling human EXO1 sumoylation in vivo and demonstrate conservation of this mechanism in yeast by the Ubc9-Siz1/Siz2 using an in vitro reconstituted system. Furthermore, we show physical interaction between EXO1 and the de-sumoylating enzyme SENP6 both in vitro and in vivo, promoting EXO1 stability. Finally, we identify the major sites of sumoylation in EXO1 and show that ectopic expression of a sumoylation-deficient form of EXO1 rescues the DNA damage-induced chromosomal aberrations observed upon wt-EXO1 expression. Thus, our study identifies a novel layer of regulation of EXO1, making the pathways that regulate its function an ideal target for therapeutic intervention.
Links
EE2.3.30.0009, research and development projectName: Zaměstnáním čerstvých absolventů doktorského studia k vědecké excelenci
GAP207/12/2323, research and development projectName: Endonuleazová a translokázová aktivita v restričních-modifikáčních komplexéch typu I
Investor: Czech Science Foundation
GA13-26629S, research and development projectName: SUMO a stability genomu
Investor: Czech Science Foundation
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