Lam L T, Bresnick E H
University of Wisconsin Medical School, Department of Pharmacology, Madison, Wisconsin 53706, USA.
J Biol Chem. 1998 Sep 11;273(37):24223-31. doi: 10.1074/jbc.273.37.24223.
Previously, we characterized a DNA-binding protein, HS2NF5, that bound tightly to a conserved region within hypersensitive site 2 (HS2) of the human beta-globin locus control region (LCR) (Lam, L. T. , and Bresnick, E. H. (1996) J. Biol. Chem. 271, 32421-32429). The beta-globin LCR controls the chromatin structure, transcription, and replication of the beta-globin genes. We have now purified HS2NF5 to near-homogeneity from fetal bovine thymus. Two polypeptides of 56 and 61 kDa copurified with the DNA binding activity. The two proteins bound to the LCR recognition site with an affinity (3.1 nM) and specificity similar to mouse erythroleukemia cell HS2NF5. The amino acid sequences of tryptic peptides of purified HS2NF5 revealed it to be identical to the murine homolog of the suppressor of hairless transcription factor, also known as recombination signal binding protein Jkappa or C promoter binding factor 1 (CBF1). The CBF1 site within HS2 resides near sites for hematopoietic regulators such as GATA-1, NF-E2, and TAL1. An additional conserved, high affinity CBF1 site was localized within HS4 of the LCR. As CBF1 is a downstream target of the Notch signaling pathway, we propose that Notch may modulate LCR activity during hematopoiesis.
此前,我们鉴定了一种DNA结合蛋白HS2NF5,它能紧密结合于人β-珠蛋白基因座控制区(LCR)超敏位点2(HS2)内的一个保守区域(林,L.T.,和布雷斯尼克,E.H.(1996)《生物化学杂志》271,32421 - 32429)。β-珠蛋白LCR控制着β-珠蛋白基因的染色质结构、转录和复制。我们现在已从胎牛胸腺中将HS2NF5纯化至接近均一性。两种分子量分别为56 kDa和61 kDa的多肽与DNA结合活性一起共纯化。这两种蛋白质以3.1 nM的亲和力结合到LCR识别位点,其特异性与小鼠红白血病细胞的HS2NF5相似。纯化的HS2NF5胰蛋白酶肽段的氨基酸序列显示,它与无毛转录因子抑制子的鼠同源物相同,后者也被称为重组信号结合蛋白Jκ或C启动子结合因子1(CBF1)。HS2内的CBF1位点位于造血调节因子如GATA - 1、NF - E2和TAL1的位点附近。LCR的HS4内还定位了另一个保守的高亲和力CBF1位点。由于CBF1是Notch信号通路的下游靶点,我们推测Notch可能在造血过程中调节LCR活性。