Werr W, Springer B, Schürmann J, Bellmann R
Institut für Genetik, Universität zu Köln, Federal Republic of Germany.
Mol Gen Genet. 1988 May;212(2):342-50. doi: 10.1007/BF00334705.
Nuclear proteins were extracted from isolated nuclei of immature maize kernels. The promoter region (1.5 kb) of the Shrunken gene, which is highly transcribed in the developing endosperm of the kernel, was scanned for protein-DNA interactions. Several promoter fragments showed protein-DNA complex formation in gel retardation experiments. Two different nucleo-protein complexes (MNP1 and MNP2) have been distinguished in competition and DNase I footprinting experiments. Both nuclear DNA-binding activities are able to recognize multiple sites distributed over a 1.5 kb upstream region of the Shrunken gene. Some of the binding sites established in the in vitro reconstitution experiments are located near to DNase I hypersensitive sites found in the promoter of the Shrunken gene (Frommer and Starlinger 1988).
从未成熟玉米籽粒分离出的细胞核中提取核蛋白。对在籽粒发育胚乳中高转录的皱缩基因的启动子区域(1.5 kb)进行蛋白质-DNA相互作用扫描。在凝胶阻滞实验中,几个启动子片段显示出蛋白质-DNA复合物的形成。在竞争和DNase I足迹实验中区分出两种不同的核蛋白复合物(MNP1和MNP2)。两种核DNA结合活性都能够识别分布在皱缩基因上游1.5 kb区域的多个位点。体外重组实验中确定的一些结合位点位于皱缩基因启动子中发现的DNase I超敏位点附近(弗罗默和施塔林格,1988年)。