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dc.contributor.authorRajarajan, Prashanth
dc.contributor.authorBorrman, Tyler M.
dc.contributor.authorWeng, Zhiping
dc.contributor.authorAkbarian, Schahram
dc.date2022-08-11T08:07:59.000
dc.date.accessioned2022-08-23T15:38:03Z
dc.date.available2022-08-23T15:38:03Z
dc.date.issued2018-12-14
dc.date.submitted2019-01-09
dc.identifier.citation<p>Science. 2018 Dec 14;362(6420). pii: eaat4311. doi: 10.1126/science.aat4311. <a href="https://doi.org/10.1126/science.aat4311">Link to article on publisher's site</a></p>
dc.identifier.issn0036-8075 (Linking)
dc.identifier.doi10.1126/science.aat4311
dc.identifier.pmid30545851
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25853
dc.description<p>Full author list omitted for brevity. For the full list of authors, see article.</p>
dc.description.abstractTo explore the developmental reorganization of the three-dimensional genome of the brain in the context of neuropsychiatric disease, we monitored chromosomal conformations in differentiating neural progenitor cells. Neuronal and glial differentiation was associated with widespread developmental remodeling of the chromosomal contact map and included interactions anchored in common variant sequences that confer heritable risk for schizophrenia. We describe cell type-specific chromosomal connectomes composed of schizophrenia risk variants and their distal targets, which altogether show enrichment for genes that regulate neuronal connectivity and chromatin remodeling, and evidence for coordinated transcriptional regulation and proteomic interaction of the participating genes. Developmentally regulated chromosomal conformation changes at schizophrenia-relevant sequences disproportionally occurred in neurons, highlighting the existence of cell type-specific disease risk vulnerabilities in spatial genome organization.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=30545851&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1126/science.aat4311
dc.subjectBioinformatics
dc.subjectComputational Biology
dc.subjectGenetic Phenomena
dc.subjectGenomics
dc.subjectIntegrative Biology
dc.subjectMental Disorders
dc.subjectNervous System
dc.subjectNervous System Diseases
dc.subjectNeuroscience and Neurobiology
dc.subjectStructural Biology
dc.subjectSystems Biology
dc.titleNeuron-specific signatures in the chromosomal connectome associated with schizophrenia risk
dc.typeJournal Article
dc.source.journaltitleScience (New York, N.Y.)
dc.source.volume362
dc.source.issue6420
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/bioinformatics_pubs/145
dc.identifier.contextkey13591447
html.description.abstract<p>To explore the developmental reorganization of the three-dimensional genome of the brain in the context of neuropsychiatric disease, we monitored chromosomal conformations in differentiating neural progenitor cells. Neuronal and glial differentiation was associated with widespread developmental remodeling of the chromosomal contact map and included interactions anchored in common variant sequences that confer heritable risk for schizophrenia. We describe cell type-specific chromosomal connectomes composed of schizophrenia risk variants and their distal targets, which altogether show enrichment for genes that regulate neuronal connectivity and chromatin remodeling, and evidence for coordinated transcriptional regulation and proteomic interaction of the participating genes. Developmentally regulated chromosomal conformation changes at schizophrenia-relevant sequences disproportionally occurred in neurons, highlighting the existence of cell type-specific disease risk vulnerabilities in spatial genome organization.</p>
dc.identifier.submissionpathbioinformatics_pubs/145
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.source.pageseaat4311


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