Shick V V, Belyavsky A V, Mirzabekov A D
J Mol Biol. 1985 Sep 20;185(2):329-39. doi: 10.1016/0022-2836(85)90407-3.
The binding sites for histones and high mobility group proteins (HMG) 14 and 17 have been located on DNA in the nucleosomal cores and H1/H5-containing nucleosomes. The nucleosomes were specifically associated with two molecules of the non-histone proteins HMG 14 and/or HMG 17 when followed by DNA-protein crosslinking and immunoaffinity isolation of the crosslinked HMG-DNA complexes. HMGs 14 and 17 were shown to be crosslinked in a similar manner to each core DNA strand at four sites: to both 3' and 5' DNA ends and also at distances of about 25 and 125 nucleotides from the 5' termini of the DNA. These sites are designated as HMG(143), (0), (25) and (125). The site HMG(125) is located at the place where no significant histone-DNA crosslinking was observed. The HMG(125) and HMG(25) sites lie opposite one another on the complementary DNA strands across the minor DNA groove and are placed, similarly to histones, on the inner side of the DNA superhelix in the nucleosome. The crosslinking of HMG 17 to the 3' ends of the DNA is much weaker than that of HMG 14. These data indicate that each of two molecules of HMG 14 and/or HMG 17 is bound to the double-stranded core DNA at two discrete sites: to the 3' and 5' ends of the DNA and at a distance of 20 to 25 base-pairs from each DNA terminus inside the nucleosome on a histone-free DNA region. Binding of HMG 14 or 17 does not induce any detectable rearrangement of histones on DNA and both HMGs seem to choose the same sites for attachment in nucleosomal cores and H1/H5-containing nucleosomes.
组蛋白以及高迁移率族蛋白(HMG)14和17的结合位点已定位在核小体核心以及含H1/H5的核小体中的DNA上。当进行DNA-蛋白质交联并对交联的HMG-DNA复合物进行免疫亲和分离时,核小体与两个非组蛋白分子HMG 14和/或HMG 17特异性结合。结果显示,HMG 14和17以类似方式在四个位点与每条核心DNA链交联:与DNA的3'和5'末端,以及距DNA 5'末端约25和125个核苷酸处交联。这些位点被指定为HMG(143)、(0)、(25)和(125)。位点HMG(125)位于未观察到明显组蛋白-DNA交联的位置。HMG(125)和HMG(25)位点在互补DNA链上相对,横跨DNA小沟,并且与组蛋白类似,位于核小体中DNA超螺旋的内侧。HMG 17与DNA 3'末端的交联比HMG 14弱得多。这些数据表明,HMG 14和/或HMG 17的两个分子各自在两个离散位点与双链核心DNA结合:与DNA的3'和5'末端,以及在核小体中无组蛋白的DNA区域内距每个DNA末端20至25个碱基对处。HMG 14或17的结合不会诱导DNA上组蛋白发生任何可检测到的重排,并且两种HMG似乎在核小体核心以及含H1/H5的核小体中选择相同的附着位点。