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                  <mods:namePart>Fernandez-Capetillo, Oscar</mods:namePart>
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                  <mods:namePart>Chen, Hua-Tang</mods:namePart>
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                  <mods:namePart>Celeste, Arkady</mods:namePart>
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                  <mods:namePart>Ward, Irene</mods:namePart>
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                  <mods:namePart>Romanienko, Peter J</mods:namePart>
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                  <mods:namePart>Morales, Julio C</mods:namePart>
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                  <mods:namePart>Naka, Kazuhito</mods:namePart>
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                  <mods:namePart>Xia, Zhenfang</mods:namePart>
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                  <mods:namePart>Camerini-Otero, R Daniel</mods:namePart>
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                  <mods:namePart>Carpenter, Phillip B</mods:namePart>
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                  <mods:namePart>Bonner, William M</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Chen, Junjie</mods:namePart>
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               <mods:name>
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                  <mods:namePart>Nussenzweig, André</mods:namePart>
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                  <mods:dateAccessioned encoding="iso8601">2024-02-09T14:41:51Z</mods:dateAccessioned>
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                  <mods:dateIssued encoding="iso8601">2002-12</mods:dateIssued>
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               <mods:identifier type="citation">Nat Cell Biol  . 2002;4(12):993-7.</mods:identifier>
               <mods:identifier type="doi">10.1038/ncb884</mods:identifier>
               <mods:identifier type="issn">1465-7392</mods:identifier>
               <mods:identifier type="journal">Nature cell biology</mods:identifier>
               <mods:identifier type="pubmedID">12447390</mods:identifier>
               <mods:identifier type="uri">http://hdl.handle.net/20.500.12105/17703</mods:identifier>
               <mods:abstract>Activation of the ataxia telangiectasia mutated (ATM) kinase triggers diverse cellular responses to ionizing radiation (IR), including the initiation of cell cycle checkpoints. Histone H2AX, p53 binding-protein 1 (53BP1) and Chk2 are targets of ATM-mediated phosphorylation, but little is known about their roles in signalling the presence of DNA damage. Here, we show that mice lacking either H2AX or 53BP1, but not Chk2, manifest a G2-M checkpoint defect close to that observed in ATM(-/-) cells after exposure to low, but not high, doses of IR. Moreover, H2AX regulates the ability of 53BP1 to efficiently accumulate into IR-induced foci. We propose that at threshold levels of DNA damage, H2AX-mediated concentration of 53BP1 at double-strand breaks is essential for the amplification of signals that might otherwise be insufficient to prevent entry of damaged cells into mitosis.</mods:abstract>
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               <mods:titleInfo>
                  <mods:title>DNA damage-induced G2-M checkpoint activation by histone H2AX and 53BP1.</mods:title>
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               <mods:genre>journal article</mods:genre>
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