5′hs5 of the human β-globin locus control region is dispensable for the formation of the β-globin active chromatin hub5u2032hs5人类β-globin轨迹控制区域是可有可无的β-globin活性染色质中心的形成.pdfVIP
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5′hs5 of the human β-globin locus control region is dispensable for the formation of the β-globin active chromatin hub5u2032hs5人类β-globin轨迹控制区域是可有可无的β-globin活性染色质中心的形成
59HS5 of the Human b-globin Locus Control Region Is
Dispensable for the Formation of the b-globin Active
Chromatin Hub
1 2 2 1
Ping Kei Chan , Albert Wai , Sjaak Philipsen *, Kian-Cheng Tan-Un *
1 Department of Zoology, Kadoorie Biological Science Building, The University of Hong Kong, Hong Kong Special Administrative Region (SAR), China, 2 Erasmus MC,
Department of Cell Biology, Rotterdam, The Netherlands
Abstract
Hypersensitive site 5 (59HS5) of the b-globin Locus Control Region functions as a developmental stage-specific border in
erythroid cells. Here, we have analyzed the role of 59HS5 in the three dimensional organization of the b-gene locus using the
Chromatin Conformation Capture (3C) technique. The results show that when 59HS5 is deleted from the locus, both remote
and internal regulatory elements are still able to interact with each other in a three-dimensional configuration termed the
Active Chromatin Hub. Thus, the absence of 59HS5 does not have an appreciable effect on the three dimensional
organization of the b-globin locus. This rules out models in which 59HS5 nucleates interactions with remote and/or internal
regulatory elements. We also determined the binding of CTCF, the only defined insulator protein in mammalian cells, to
59HS5 by using chromatin immunoprecipitation (ChIP) assays. We detect low levels of CTCF binding to 59HS5 in primitive
erythroid cells, in which it functions as a border element. Surprisingly, we also observe binding levels of CTCF to 59HS5 in
definitive erythroid cells. Thus, binding of CTCF to 59HS5 per se does not render it a functional border element. This is
consistent with the previous data suggesting that CTCF has dual functionality.
Citation: Chan PK, Wai A, Philipsen S
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