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Gfi1 的表达受五个不同的调控区域控制,这些区域分布在 100 千碱基上,Scl/Tal1、Gata2、PU.1、Erg、Meis1 和 Runx1 在早期造血细胞中作为上游调节因子发挥作用。

Gfi1 expression is controlled by five distinct regulatory regions spread over 100 kilobases, with Scl/Tal1, Gata2, PU.1, Erg, Meis1, and Runx1 acting as upstream regulators in early hematopoietic cells.

机构信息

University of Cambridge, Department of Haematology, Cambridge Institute for Medical Research, Cambridge, United Kingdom.

出版信息

Mol Cell Biol. 2010 Aug;30(15):3853-63. doi: 10.1128/MCB.00032-10. Epub 2010 Jun 1.

Abstract

The growth factor independence 1 (Gfi1) gene was originally discovered in the hematopoietic system, where it functions as a key regulator of stem cell homeostasis, as well as neutrophil and T-cell development. Outside the blood system, Gfi1 is essential for inner-ear hair and intestinal secretory cell differentiation. To understand the regulatory hierarchies within which Gfi1 operates to control these diverse biological functions, we used a combination of comparative genomics, locus-wide chromatin immunoprecipitation assays, functional validation in cell lines, and extensive transgenic mouse assays to identify and characterize the complete ensemble of Gfi1 regulatory elements. This concerted effort identified five distinct regulatory elements spread over 100kb each driving expression in transgenic mice to a subdomain of endogenous Gfi1. Detailed characterization of an enhancer 35 kb upstream of Gfi1 demonstrated activity in the dorsal aorta region and fetal liver in transgenic mice, which was bound by key stem cell transcription factors Scl/Tal1, PU.1/Sfpi1, Runx1, Erg, Meis1, and Gata2. Taken together, our results reveal the regulatory regions responsible for Gfi1 expression and importantly establish that Gfi1 expression at the sites of hematopoietic stem cell (HSC) emergence is controlled by key HSC regulators, thus integrating Gfi1 into the wider HSC regulatory networks.

摘要

生长因子独立性 1(Gfi1)基因最初在造血系统中被发现,在造血系统中,它作为干细胞动态平衡以及中性粒细胞和 T 细胞发育的关键调节剂发挥作用。在血液系统之外,Gfi1 对于内耳毛细胞和肠道分泌细胞的分化是必不可少的。为了了解 Gfi1 控制这些不同生物学功能的调控层次,我们使用了比较基因组学、全基因座染色质免疫沉淀分析、细胞系中的功能验证以及广泛的转基因小鼠实验,以鉴定和表征 Gfi1 调控元件的完整集合。这项协同努力确定了五个不同的调控元件,每个元件跨越 100kb,在转基因小鼠中驱动内源性 Gfi1 的一个亚域表达。对 Gfi1 上游 35kb 的增强子的详细特征分析表明,其在转基因小鼠的背主动脉区域和胎肝中具有活性,该活性被关键的干细胞转录因子 Scl/Tal1、PU.1/Sfpi1、Runx1、Erg、Meis1 和 Gata2 结合。总之,我们的结果揭示了负责 Gfi1 表达的调控区域,并重要地证实了造血干细胞(HSC)出现部位的 Gfi1 表达受关键 HSC 调控因子的控制,从而将 Gfi1 整合到更广泛的 HSC 调控网络中。

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