<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-07-23T17:11:54Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/8538" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/8538</identifier><datestamp>2024-11-29T14:10:33Z</datestamp><setSpec>com_20.500.12105_2173</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19597</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Hernández-Pérez, Santiago</subfield>
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      <subfield code="a">Cabrera, Elisa</subfield>
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      <subfield code="a">Amoedo, Hugo</subfield>
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      <subfield code="a">Rodríguez-Acebes, Sara</subfield>
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      <subfield code="a">Koundrioukoff, Stephane</subfield>
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      <subfield code="a">Debatisse, Michelle</subfield>
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      <subfield code="a">Mendez, Juan</subfield>
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      <subfield code="a">Freire, Raimundo</subfield>
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      <subfield code="c">2016-10</subfield>
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      <subfield code="a">DNA replication control is a key process in maintaining genomic integrity. Monitoring DNA replication initiation is particularly important as it needs to be coordinated with other cellular events and should occur only once per cell cycle. Crucial players in the initiation of DNA replication are the ORC protein complex, marking the origin of replication, and the Cdt1 and Cdc6 proteins, that license these origins to replicate by recruiting the MCM2-7 helicase. To accurately achieve its functions, Cdt1 is tightly regulated. Cdt1 levels are high from metaphase and during G1 and low in S/G2 phases of the cell cycle. This control is achieved, among other processes, by ubiquitination and proteasomal degradation. In an overexpression screen for Cdt1 deubiquitinating enzymes, we isolated USP37, to date the first ubiquitin hydrolase controlling Cdt1. USP37 overexpression stabilizes Cdt1, most likely a phosphorylated form of the protein. In contrast, USP37 knock down destabilizes Cdt1, predominantly during G1 and G1/S phases of the cell cycle. USP37 interacts with Cdt1 and is able to de-ubiquitinate Cdt1 in vivo and, USP37 is able to regulate the loading of MCM complexes onto the chromatin. In addition, downregulation of USP37 reduces DNA replication fork speed. Taken together, here we show that the deubiquitinase USP37 plays an important role in the regulation of DNA replication. Whether this is achieved via Cdt1, a central protein in this process, which we have shown to be stabilized by USP37, or via additional factors, remains to be tested.</subfield>
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      <subfield code="a">Mol Oncol. 2016;10(8):1196-206.</subfield>
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      <subfield code="a">10.1016/j.molonc.2016.05.008</subfield>
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      <subfield code="a">Molecular oncology</subfield>
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      <subfield code="a">27296872</subfield>
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      <subfield code="a">http://hdl.handle.net/20.500.12105/8538</subfield>
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      <subfield code="a">DNA damage</subfield>
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      <subfield code="a">DNA damage response</subfield>
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      <subfield code="a">Initiation of DNA replication</subfield>
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      <subfield code="a">Proteasome</subfield>
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      <subfield code="a">Protein degradation</subfield>
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      <subfield code="a">Ubiquitin hydrolase</subfield>
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      <subfield code="a">USP37 deubiquitinates Cdt1 and contributes to regulate DNA replication</subfield>
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