Ristiniemi J, Oikarinen J
Collagen Research Unit and Biocenter, University of Oulu, Finland.
J Biol Chem. 1989 Feb 5;264(4):2164-74.
It has previously been demonstrated that nuclear factor I (NF I) or a related protein binds to a region between -315 and -295 from the start of transcription in the mouse alpha 2(I) collagen gene promoter. In the present work we have purified this factor to homogeneity from rat liver. DNA sequence-specific proteins were isolated from nuclear extracts using heparin-agarose affinity chromatography and two successive chromatographies on a recognition site affinity matrix. Approximately 160 micrograms of the DNA binding proteins was obtained from 100 g of rat liver. More than 1700-fold purification over the nuclear extract and 58% recovery of the DNA binding activity was achieved. The purified preparation contained five to six protein components ranging in molecular weight from 30,000 to 35,000, as determined by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. It was demonstrated using DNase I footprint analysis that the factor binds to the putative NF I binding site in the mouse alpha 2(I) collagen promoter. It has a dissociation constant of 7 nM for a short DNA fragment containing this binding site, while a constant of 0.45 nM was obtained for a similar-sized fragment containing the nuclear NF I consensus binding sequence. The purified factor is identical to histone H1 in several respects. They share similar amino acid compositions and they give similar V8-protease and N-bromosuccinimide peptides. In addition, antibodies raised to bovine histone H1 recognize the purified factor and interfere with its binding to DNA. Methylation interference and preparative gel shift assay show that histone H1 binds to the specific sequence from the preparation of the alpha 2(I) collagen promoter binding factor. It is thus evident from the present results, that histone H1 binds to the NF I recognition sequence in the mouse alpha 2(I) collagen promoter.
先前已经证明,核因子I(NF I)或一种相关蛋白与小鼠α2(I)型胶原基因启动子转录起始点上游-315至-295区域结合。在本研究中,我们从大鼠肝脏中纯化了这种因子,使其达到同质。使用肝素-琼脂糖亲和色谱法和在识别位点亲和基质上的两次连续色谱法从核提取物中分离出DNA序列特异性蛋白。从100克大鼠肝脏中获得了约160微克的DNA结合蛋白。相对于核提取物实现了超过1700倍的纯化,并且DNA结合活性的回收率为58%。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳测定,纯化制剂包含五到六种蛋白质成分,分子量范围为30,000至35,000。使用DNase I足迹分析表明,该因子与小鼠α2(I)型胶原启动子中假定的NF I结合位点结合。对于包含该结合位点的短DNA片段,其解离常数为7 nM,而对于包含核NF I共有结合序列的类似大小片段,获得的常数为0.45 nM。纯化的因子在几个方面与组蛋白H1相同。它们具有相似的氨基酸组成,并且给出相似的V8蛋白酶和N-溴代琥珀酰亚胺肽段。此外,针对牛组蛋白H1产生的抗体识别纯化的因子并干扰其与DNA的结合。甲基化干扰和制备性凝胶迁移分析表明,组蛋白H1与α2(I)型胶原启动子结合因子制剂中的特定序列结合。因此,从目前的结果可以明显看出,组蛋白H1与小鼠α2(I)型胶原启动子中的NF I识别序列结合。