Literature DB >> 28137913

Chromatin Domain Organization of the TCRb Locus and Its Perturbation by Ectopic CTCF Binding.

Pratishtha Rawat1, Manisha Jalan1, Ananya Sadhu1, Abhilasha Kanaujia1, Madhulika Srivastava2.   

Abstract

CTCF-mediated chromatin interactions influence organization and function of mammalian genome in diverse ways. We analyzed the interactions among CTCF binding sites (CBS) at the murine TCRb locus to discern the role of CTCF-mediated interactions in the regulation of transcription and VDJ recombination. Chromosome conformation capture analysis revealed thymocyte-specific long-range intrachromosomal interactions among various CBS across the locus that were relevant for defining the limit of the enhancer Eb-regulated recombination center (RC) and for facilitating the spatial proximity of TCRb variable (V) gene segments to the RC. Ectopic CTCF binding in the RC region, effected via genetic manipulation, altered CBS-directed chromatin loops, interfered with RC establishment, and reduced the spatial proximity of the RC with Trbv segments. Changes in chromatin loop organization by ectopic CTCF binding were relatively modest but influenced transcription and VDJ recombination dramatically. Besides revealing the importance of CTCF-mediated chromatin organization for TCRb regulation, the observed chromatin loops were consistent with the emerging idea that CBS orientations influence chromatin loop organization and underscored the importance of CBS orientations for defining chromatin architecture that supports VDJ recombination. Further, our study suggests that in addition to mediating long-range chromatin interactions, CTCF influences intricate configuration of chromatin loops that govern functional interactions between elements.
Copyright © 2017 American Society for Microbiology.

Entities:  

Keywords:  CTCF; VDJ recombination; antigen receptor loci; chromatin loop; chromatin organization

Mesh:

Substances:

Year:  2017        PMID: 28137913      PMCID: PMC5394274          DOI: 10.1128/MCB.00557-16

Source DB:  PubMed          Journal:  Mol Cell Biol        ISSN: 0270-7306            Impact factor:   4.272


  53 in total

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