Kolomiĭtseva G I, Prusov A N, Smirnova T A, Vaniushin B F
Bioorg Khim. 2010 Sep-Oct;36(5):672-80. doi: 10.1134/s1068162010050109.
Incubation in vitro of rat liver nuclei in the presence of S-adenosyl[methyl-(3)H]methionine ([(3)H] SAM) leads to incorporation of the radioactive label not only into core-histones H3 and H4, but also into linker histone H1. Addition of distamycine A to the incubation medium stimulates label incorporation into histone H1 ~ in 6 times and into histone H3 ~ in 2 times. The presence of distamycine facilitates histone H1 extraction by polyglutamic acid (poly(Glu)) and decreases of UV-induced DNA-histone cross-links formation. These effects give evidence of weakening of H1-chromatin interaction by distamycin to be results of histone H1 position change relative to nucleosome and(or) disturbance of histones H1-H3 interactions so as these histones are exposed to additional methylation.
在含有S-腺苷基[甲基-(3)H]甲硫氨酸([(3)H] SAM)的条件下对大鼠肝细胞核进行体外温育,不仅会使放射性标记掺入核心组蛋白H3和H4,还会掺入连接组蛋白H1。向温育培养基中添加偏端霉素A可刺激标记物掺入组蛋白H1的量增加约6倍,掺入组蛋白H3的量增加约2倍。偏端霉素的存在有利于通过聚谷氨酸(聚(Glu))提取组蛋白H1,并减少紫外线诱导的DNA-组蛋白交联的形成。这些效应表明,偏端霉素削弱H1-染色质相互作用是组蛋白H1相对于核小体的位置改变和(或)组蛋白H1-H3相互作用受到干扰的结果,从而使这些组蛋白易于发生额外的甲基化。