Bianchi F, Rousseaux-Prevost R, Bailly C, Rousseaux J
Institut de Recherches sur le Cancer, Lille, France.
Biochem Biophys Res Commun. 1994 Jun 30;201(3):1197-204. doi: 10.1006/bbrc.1994.1832.
The interaction of two classes of human sperm protamines, P1 (HP1) and P2 (HP2, HP3, HP4), with DNA was investigated. Gel mobility shift assays with a range of DNA fragments of defined sizes show that, whatever its length, all the DNA is complexed with protamines at arginine to phosphate ratio of 0.1. Further addition of protamine molecules leads to a precipitation of the protamine-DNA complexes for arginine-phosphate ratio > or = 1.2. Fluorescence studies using the dye Hoescht 33258 as a fluorophore and DNAase I footprinting experiments suggest that P1 and P2 protamines bind at the DNA surface without apparent location in the minor or major groove of DNA. No differences in protamine-DNA interaction were observed between the two classes of human protamines P1 and P2. Moreover the binding to DNA was not influenced by the presence of zinc which induces the formation of a zinc-finger structure in protamine P2.
研究了两类人类精子鱼精蛋白P1(HP1)和P2(HP2、HP3、HP4)与DNA的相互作用。使用一系列特定大小的DNA片段进行凝胶迁移率变动分析表明,无论DNA长度如何,所有DNA在精氨酸与磷酸的比例为0.1时都与鱼精蛋白复合。进一步添加鱼精蛋白分子会导致精氨酸 - 磷酸比例大于或等于1.2时鱼精蛋白 - DNA复合物沉淀。使用染料Hoechst 33258作为荧光团的荧光研究和DNA酶I足迹实验表明,P1和P2鱼精蛋白结合在DNA表面,在DNA的小沟或大沟中没有明显的定位。在两类人类鱼精蛋白P1和P2之间未观察到鱼精蛋白 - DNA相互作用的差异。此外,锌的存在不影响与DNA的结合,锌会诱导鱼精蛋白P2中锌指结构的形成。