KLISZCZAK, Maciej, Hana SEDLÁČKOVÁ, Ganesha P. PITCHAI, Werner W. STREICHER, Lumír KREJČÍ and Ian D. HICKSON. Interaction of RECQ4 and MCM10 is important for efficient DNA replication origin firing in human cells. Oncotarget. New York: Impact Journals LLC, 2015, vol. 6, No 38, p. 40464-40479. ISSN 1949-2553. Available from: https://dx.doi.org/10.18632/oncotarget.6342.
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Basic information
Original name Interaction of RECQ4 and MCM10 is important for efficient DNA replication origin firing in human cells
Authors KLISZCZAK, Maciej (208 Denmark), Hana SEDLÁČKOVÁ (203 Czech Republic, belonging to the institution), Ganesha P. PITCHAI (208 Denmark), Werner W. STREICHER (208 Denmark), Lumír KREJČÍ (203 Czech Republic, guarantor, belonging to the institution) and Ian D. HICKSON (208 Denmark).
Edition Oncotarget, New York, Impact Journals LLC, 2015, 1949-2553.
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: 5.008
RIV identification code RIV/00216224:14110/15:00081496
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.18632/oncotarget.6342
UT WoS 000366115500008
Keywords in English DNA replication; RecQ helicases; minichromosome maintenance proteins; Chromosome Section
Tags EL OK, podil
Tags International impact, Reviewed
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 20/1/2016 14:49.
Abstract
DNA replication is a highly coordinated process that is initiated at multiple replication origins in eukaryotes. These origins are bound by the origin recognition complex (ORC), which subsequently recruits the Mcm2-7 replicative helicase in a Cdt1/Cdc6-dependent manner. In budding yeast, two essential replication factors, Sld2 and Mcm10, are then important for the activation of replication origins. In humans, the putative Sld2 homolog, RECQ4, interacts with MCM10. Here, we have identified two mutants of human RECQ4 that are deficient in binding to MCM10. We show that these RECQ4 variants are able to complement the lethality of an avian cell RECQ4 deletion mutant, indicating that the essential function of RECQ4 in vertebrates is unlikely to require binding to MCM10. Nevertheless, we show that the RECQ4-MCM10 interaction is important for efficient replication origin firing.
Links
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
MUNI/M/1894/2014, interní kód MUName: Development of new MUS81 nuclease inhibitors as chemical biology probe with clinical progression
Investor: Masaryk University, INTERDISCIPLINARY - Interdisciplinary research projects
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