King's College London, The James Black Centre, UK.
Blood Cells Mol Dis. 2010 Aug 15;45(2):140-6. doi: 10.1016/j.bcmd.2010.05.006. Epub 2010 Jun 12.
BCL11A is a major regulator of fetal hemoglobin production. Reduced levels of BCL11A have been shown to delay switching from fetal to adult hemoglobin, suggesting that it acts as a stage-specific repressor of gamma globin expression. We have carried out a survey of BCL11A binding in the globin, BCL11A and GATA1 loci by ChIP-on-chip analysis in primary human erythroid cells. We found strong occupancy in both alpha and beta globin upstream regulatory regions as well as in regions involved in switching and hereditary persistence of fetal hemoglobin. Genetic studies have identified a restricted 14kb region in BCL11A intron 2 as being highly associated with HbF levels. Strong GATA-1 binding and acetylated histone H3 was found in this area, which could be indicative of a regulatory element, changes in which might be responsible for the overall regulation of BCL11A. We also observed BCL11A and GATA-1 binding in a known auto-regulatory promoter element of the GATA1 locus.
BCL11A 是胎儿血红蛋白产生的主要调节因子。研究表明,BCL11A 水平降低会延迟从胎儿血红蛋白向成人血红蛋白的转换,这表明它作为γ珠蛋白表达的阶段特异性抑制剂发挥作用。我们通过在原代人红细胞中的染色质免疫沉淀芯片分析,对珠蛋白、BCL11A 和 GATA1 基因座中的 BCL11A 结合进行了调查。我们发现,BCL11A 在α和β珠蛋白的上游调控区以及在与开关和遗传性胎儿血红蛋白持续存在相关的区域均有强烈的占据。遗传研究已经确定了 BCL11A 内含子 2 中一个受限的 14kb 区域与 HbF 水平高度相关。在该区域发现了强烈的 GATA-1 结合和乙酰化组蛋白 H3,这可能表明存在一个调节元件,其变化可能负责 BCL11A 的整体调节。我们还观察到 BCL11A 和 GATA-1 在 GATA1 基因座的一个已知的自身调节启动子元件中的结合。