Camerini-Otero R D, Felsenfeld G
Nucleic Acids Res. 1977;4(5):1159-81. doi: 10.1093/nar/4.5.1159-a.
We have formed complexes of relaxed closed circular Col E1 DNA with various combinations of histones, and examined the effects of treating the complexes with nicking-closing enzyme. Germond et al (1) have shown that when a mixture of the four core histones of the nucleosome (HIA, H2B, H3 and H4) is used in such an experiment, the subsequently isolated DNA is supercoiled. We find that the arginine-rich histone pair, H3 and H4, is sufficient to induce the supercoiling observed in this experiment. Both H3 and H4 are required, and in the absence of either, no other histones are effective. H3 and and H4 are as efficient, per unit weight, as a mixture of the four histones in inducing supercoils. We also show that there is a large difference between the DNA bending energy needed to form a nucleosome and that needed to form one turn of normal superhelical DNA. These two processes are energetically quite distinct and probably separable. We estimate the free energy of interaction between DNA-bound histone pairs, and find that one or two such interactions would generate enough energy to fold the DNA into a nucleosome.
我们已将松弛的闭环Col E1 DNA与各种组蛋白组合形成复合物,并研究了用切口封闭酶处理这些复合物的效果。Germond等人(1)表明,在这样的实验中使用核小体的四种核心组蛋白(H1A、H2B、H3和H4)的混合物时,随后分离出的DNA是超螺旋的。我们发现富含精氨酸的组蛋白对H3和H4足以诱导该实验中观察到的超螺旋。H3和H4两者都是必需的,缺少其中任何一个,其他组蛋白都无效。就单位重量而言,H3和H4在诱导超螺旋方面与四种组蛋白的混合物一样有效。我们还表明,形成一个核小体所需的DNA弯曲能量与形成一圈正常超螺旋DNA所需的能量之间存在很大差异。这两个过程在能量上截然不同,可能是可分离的。我们估计了与DNA结合的组蛋白对之间的相互作用自由能,发现一两个这样的相互作用将产生足够的能量将DNA折叠成一个核小体。