Thakur M K, Prasad S
Department of Zoology, Banaras Hindu University, Varanasi, India.
Mutat Res. 1989 Mar;219(2):107-11. doi: 10.1016/0921-8734(89)90021-0.
Liver slices from young (20 weeks) and old (117 weeks) rats were incubated with [methyl-14C]methionine in the absence or presence of spermine or sodium butyrate. The high-mobility-group (HMG) non-histone proteins were extracted from the liver with perchloric acid and separated by acid-urea polyacrylamide slab gel electrophoresis. Methylation of HMG proteins decreased drastically in old rats. Whereas spermine inhibited the methylation of total HMG proteins in young rats, it had no effect in old age. On the contrary, sodium butyrate did not change the incorporation of methyl groups into total HMG proteins of young rats, but inhibited that of old rats. Particularly, the incorporation of [14C]methyl groups into HMG 2 was enhanced but into other HMGs it was reduced by both effectors in young and old age. Such discrepancies in the methylation of HMG proteins and their differential modulation by spermine and butyrate might affect the higher-order organization of chromatin and consequently destabilize the expression of genes during aging.
将年轻(20周)和老年(117周)大鼠的肝脏切片在不存在或存在精胺或丁酸钠的情况下与[甲基-14C]甲硫氨酸一起孵育。用高氯酸从肝脏中提取高迁移率族(HMG)非组蛋白,并通过酸-尿素聚丙烯酰胺平板凝胶电泳进行分离。老年大鼠中HMG蛋白的甲基化显著降低。虽然精胺抑制年轻大鼠中总HMG蛋白的甲基化,但在老年时它没有作用。相反,丁酸钠不会改变年轻大鼠总HMG蛋白中甲基的掺入,但会抑制老年大鼠的。特别是,在年轻和老年时,两种效应物都增强了[14C]甲基掺入HMG 2,但减少了其掺入其他HMG。HMG蛋白甲基化的这种差异及其受精胺和丁酸盐的差异调节可能会影响染色质的高级组织,从而在衰老过程中使基因表达不稳定。