Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3260
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dc.contributor.authorChawla, B.-
dc.contributor.authorRamachandran, Rajesh-
dc.contributor.authorSandhu, K.S.-
dc.date.accessioned2020-12-21T06:30:34Z-
dc.date.available2020-12-21T06:30:34Z-
dc.date.issued2020-
dc.identifier.citationCell Reports, 33(4)en_US
dc.identifier.other10.1016/j.celrep.2020.108302-
dc.identifier.urihttps://pubmed.ncbi.nlm.nih.gov/33113374-
dc.identifier.urihttp://hdl.handle.net/123456789/3260-
dc.description.abstractThe mechanisms that guide the clonally stable random mono-allelic expression of autosomal genes remain enigmatic. We show that (1) mono-allelically expressed (MAE) genes are assorted and insulated from bi-allelically expressed (BAE) genes through CTCF-mediated chromatin loops; (2) the cell-type-specific dynamics of mono-allelic expression coincides with the gain and loss of chromatin insulator sites; (3) dosage of MAE genes is more sensitive to the loss of chromatin insulation than that of BAE genes; and (4) inactive alleles of MAE genes are significantly more insulated than active alleles and are de-repressed upon CTCF depletion. This alludes to a topology wherein the inactive alleles of MAE genes are insulated from the spatial interference of transcriptional states from the neighboring bi-allelic domains via CTCF-mediated loops. We propose that CTCF functions as a typical insulator on inactive alleles, but facilitates transcription through enhancer-linking on active allele of MAE genes, indicating widespread allele-specific regulatory roles of CTCFen_US
dc.language.isoen_USen_US
dc.publisherElsevier B.V.en_US
dc.subjectChIA-PETen_US
dc.subjectchromatin insulationen_US
dc.subjectchromatin loopsen_US
dc.subjectCTCFen_US
dc.subjectCTCF-depletionen_US
dc.subjectepigenetic regulationen_US
dc.titleCTCF-Mediated Genome Architecture Regulates the Dosage of Mitotically Stable Mono-allelic Expression of Autosomal Genesen_US
dc.typeArticleen_US
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