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dc.contributor.authorHnisz, Denes
dc.contributor.authorWeintraub, Abraham S.
dc.contributor.authorDay, Daniel S.
dc.contributor.authorValton, Anne-Laure
dc.contributor.authorBak, Rasmus O.
dc.contributor.authorLi, Charles H.
dc.contributor.authorGoldmann, Johanna
dc.contributor.authorLajoie, Bryan R.
dc.contributor.authorFan, Zi Peng
dc.contributor.authorSigova, Alla A.
dc.contributor.authorReddy, Jessica
dc.contributor.authorBorges-Rivera, Diego
dc.contributor.authorLee, Tong Ihn
dc.contributor.authorJaenisch, Rudolf
dc.contributor.authorPorteus, Matthew H.
dc.contributor.authorDekker, Job
dc.contributor.authorYoung, Richard A.
dc.date2022-08-11T08:11:00.000
dc.date.accessioned2022-08-23T17:27:53Z
dc.date.available2022-08-23T17:27:53Z
dc.date.issued2016-03-03
dc.date.submitted2016-03-23
dc.identifier.citationScience. 2016 Mar 3. pii: aad9024. <a href="http://dx.doi.org/10.1126/science.aad9024">Link to article on publisher's site</a>
dc.identifier.issn0036-8075 (Linking)
dc.identifier.doi10.1126/science.aad9024
dc.identifier.pmid26940867
dc.identifier.urihttp://hdl.handle.net/20.500.14038/49962
dc.description.abstractOncogenes are activated through well-known chromosomal alterations, including gene fusion, translocation and focal amplification. Recent evidence that the control of key genes depends on chromosome structures called insulated neighborhoods led us to investigate whether proto-oncogenes occur within these structures and if oncogene activation can occur via disruption of insulated neighborhood boundaries in cancer cells. We mapped insulated neighborhoods in T-cell acute lymphoblastic leukemia (T-ALL), and found that tumor cell genomes contain recurrent microdeletions that eliminate the boundary sites of insulated neighborhoods containing prominent T-ALL proto-oncogenes. Perturbation of such boundaries in non-malignant cells was sufficient to activate proto-oncogenes. Mutations affecting chromosome neighborhood boundaries were found in many types of cancer. Thus, oncogene activation can occur via genetic alterations that disrupt insulated neighborhoods in malignant cells.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=26940867&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1126/science.aad9024
dc.subjectBiochemistry
dc.subjectCancer Biology
dc.subjectGenetics and Genomics
dc.subjectMolecular Biology
dc.subjectStructural Biology
dc.subjectSystems Biology
dc.titleActivation of proto-oncogenes by disruption of chromosome neighborhoods
dc.typeJournal Article
dc.source.journaltitleScience (New York, N.Y.)
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/sysbio_pubs/81
dc.identifier.contextkey8368710
html.description.abstract<p>Oncogenes are activated through well-known chromosomal alterations, including gene fusion, translocation and focal amplification. Recent evidence that the control of key genes depends on chromosome structures called insulated neighborhoods led us to investigate whether proto-oncogenes occur within these structures and if oncogene activation can occur via disruption of insulated neighborhood boundaries in cancer cells. We mapped insulated neighborhoods in T-cell acute lymphoblastic leukemia (T-ALL), and found that tumor cell genomes contain recurrent microdeletions that eliminate the boundary sites of insulated neighborhoods containing prominent T-ALL proto-oncogenes. Perturbation of such boundaries in non-malignant cells was sufficient to activate proto-oncogenes. Mutations affecting chromosome neighborhood boundaries were found in many types of cancer. Thus, oncogene activation can occur via genetic alterations that disrupt insulated neighborhoods in malignant cells.</p>
dc.identifier.submissionpathsysbio_pubs/81
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentProgram in Systems Biology


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