Abstract
Hypersensitive site 5 (5′HS5) of the β-globin Locus Control Region functions as a developmental stage-specific border in erythroid cells. Here, we have analyzed the role of 5′HS5 in the three dimensional organization of the β-gene locus using the Chromatin Conformation Capture (3C) technique. The results show that when 5′HS5 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 5′HS5 does not have an appreciable effect on the three dimensional organization of the β-globin locus. This rules out models in which 5′HS5 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 5′HS5 by using chromatin immunoprecipitation (ChIP) assays. We detect low levels of CTCF binding to 5′HS5 in primitive erythroid cells, in which it functions as a border element. Surprisingly, we also observe binding levels of CTCF to 5′HS5 in definitive erythroid cells. Thus, binding of CTCF to 5′HS5 per se does not render it a functional border element. This is consistent with the previous data suggesting that CTCF has dual functionality.
Highlights
The human b-globin locus contains five genes that are arranged in the same order as their developmental expression pattern: 59-e Gc Ac-globin gene (Ac) d b-39
The resultant transcriptionally active locus is arranged in a three dimensional structure termed the active chromatin hub (ACH), in which the Locus Control Region (LCR) hypersensitive sites interact directly with the transcribed genes through a looping mechanism [6,7]
This property of the LCR may be due to the spatial organization of its hypersensitive sites, but it is possible that the locus contains elements that block LCR action in one of the directions [11]
Summary
The human b-globin locus contains five genes that are arranged in the same order as their developmental expression pattern: 59-e (embryonic) Gc Ac (foetal) d b (adult)-39. Each of the hypersensitive sites holds a unique array of transcription factor binding sites, including those for GATA1, NF-E2 and EKLF proteins This suggests that the HS in the human LCR may have different stage-specific activities and cannot be replaced functionally by each other [3,4]. The mode of action of the LCR to the b-globin genes appears to be orientation dependent as an inverted LCR is incapable of activating downstream globin genes at high levels, and the e-gene can not be activated when placed upstream of the LCR [10] This property of the LCR may be due to the spatial organization of its hypersensitive sites, but it is possible that the locus contains elements that block LCR action in one of the directions [11]
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