Prasad S, Thakur M K
Department of Zoology, Banaras Hindu University, Varanasi, India.
Biochem Int. 1988 Feb;16(2):375-82.
The in vitro acetylation of high mobility group (HMG) proteins and its modulation by sodium butyrate and hydrocortisone have been studied using liver slices of young (13-) and old (114-week-old) rats. Acetylation of total HMG proteins was significantly higher in young than old rats. HMG 1, in particular, showed greater acetylation than others. Whereas acetylation of HMG 1 and 2 decreased drastically, that of HMG 14 and 17 increased in old age. In young rats, sodium butyrate and hydrocortisone stimulated acetylation of HMG 14 and 17, and decreased that of HMG 2. Butyrate had no effect on HMG 1, but hydrocortisone decreased it. In old rats, butyrate and hydrocortisone decreased acetylation of all HMGs, except HMG 17, which was stimulated to a slight extent by butyrate.
利用幼年(13周龄)和老年(114周龄)大鼠的肝切片,研究了高迁移率族(HMG)蛋白的体外乙酰化及其受丁酸钠和氢化可的松的调节情况。幼年大鼠中总HMG蛋白的乙酰化水平显著高于老年大鼠。尤其是HMG 1,其乙酰化程度比其他蛋白更高。随着年龄增长,HMG 1和2的乙酰化水平急剧下降,而HMG 14和17的乙酰化水平则升高。在幼年大鼠中,丁酸钠和氢化可的松刺激了HMG 14和17的乙酰化,并降低了HMG 2的乙酰化。丁酸钠对HMG 1没有影响,但氢化可的松降低了其乙酰化水平。在老年大鼠中,丁酸钠和氢化可的松降低了所有HMG蛋白的乙酰化,只有HMG 17除外,丁酸钠对其有轻微的刺激作用。