Ma X J, Goodridge A G
Department of Biochemistry, University of Iowa, Iowa City 52242.
Nucleic Acids Res. 1992 Oct 11;20(19):4997-5002. doi: 10.1093/nar/20.19.4997.
Transcription of the chicken malic enzyme gene in the liver is stimulated by feeding and inhibited by starvation. Concomitant with the increase in transcription caused by refeeding, chromatin structure around the transcription start site of the malic enzyme gene is modified in the liver. Digestion of chromatin in isolated nuclei with DNase I revealed four feeding-induced DNase I hypersensitive sites (-220, -170, -130 and -70 bp) near the malic enzyme promoter. Similarly, digestion of chromatin with restriction endonucleases detected enhanced cleavage within this region when birds were refed. Micrococcal nuclease detected the presence of nucleosomes over this region in the starved state, but not in the fed state. After food was withdrawn from fed birds, nucleosomes were reformed in this region within 6 h. The speed and magnitude of the changes in nucleosomal structure in this region suggest that they did not require DNA replication.
鸡苹果酸酶基因在肝脏中的转录受进食刺激,受饥饿抑制。与重新进食引起的转录增加相伴,肝脏中苹果酸酶基因转录起始位点周围的染色质结构发生改变。用脱氧核糖核酸酶I(DNase I)消化分离细胞核中的染色质,发现在苹果酸酶启动子附近有四个进食诱导的DNase I超敏位点(-220、-170、-130和-70碱基对)。同样,当鸟类重新进食时,用限制性内切核酸酶消化染色质可检测到该区域内切割增强。微球菌核酸酶检测到在饥饿状态下该区域存在核小体,而在进食状态下则不存在。从进食的鸟类中撤走食物后,6小时内该区域重新形成核小体。该区域核小体结构变化的速度和幅度表明,它们不需要DNA复制。