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Stadhouders, R.* ; Thongjuea, S.* ; Andrieu-Soler, C.* ; Palstra, R.J.* ; Bryne, J.C.* ; van den Heuvel, A.* ; Stevens, M.* ; de Boer, E.* ; Kockx, C.* ; van der Sloot, A.* ; van den Hout, M.* ; van Ijcken, W.* ; Eick, D. ; Lenhard, B.* ; Grosveld, F.* ; Soler, E.*

Dynamic long-range chromatin interactions control Myb proto-oncogene transcription during erythroid development.

EMBO J. 31, 986-999 (2012)
DOI
Open Access Green as soon as Postprint is submitted to ZB.
The key haematopoietic regulator Myb is essential for coordinating proliferation and differentiation. ChIP-Sequencing and Chromosome Conformation Capture (3C)-Sequencing were used to characterize the structural and protein-binding dynamics of the Myb locus during erythroid differentiation. In proliferating cells expressing Myb, enhancers within the Myb-Hbs1l intergenic region were shown to form an active chromatin hub (ACH) containing the Myb promoter and first intron. This first intron was found to harbour the transition site from transcription initiation to elongation, which takes place around a conserved CTCF site. Upon erythroid differentiation, Myb expression is downregulated and the ACH destabilized. We propose a model for Myb activation by distal enhancers dynamically bound by KLF1 and the GATA1/TAL1/LDB1 complex, which primarily function as a transcription elongation element through chromatin looping.
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Publication type Article: Journal article
Document type Scientific Article
Keywords ChIP-sequencing (ChIP-Seq); chromosome conformation capture-sequencing (3C-Seq); erythroid development; long-range interactions; Myb
ISSN (print) / ISBN 0261-4189
e-ISSN 1460-2075
Quellenangaben Volume: 31, Issue: 4, Pages: 986-999 Article Number: , Supplement: ,
Publisher Wiley
Publishing Place Heidelberg, Germany
Reviewing status Peer reviewed