Zhang Y P, Lambert M A, Cairney A E, Wills D, Ray P N, Andrulis I L
Mount Sinai Hospital Research Institute, Toronto, Ontario, Canada.
Genomics. 1989 Apr;4(3):259-65. doi: 10.1016/0888-7543(89)90329-7.
The human gene for asparagine synthetase has been isolated and the molecular organization has been determined by mapping and DNA sequencing of intron-exon boundaries. The gene spans 35 kb and contains 13 exons. The structure of the human gene has a high degree of similarity to that of the hamster asparagine synthetase gene, with identical positions for all but one of the intron regions. The 5' upstream region of this gene, like other housekeeping genes, lacks conventional TATA and CAAT boxes. Comparisons of the 5' upstream sequences of the human and hamster genes show limited similarity; however, both have a very high G + C content which may play a role in expression through DNA methylation.
天冬酰胺合成酶的人类基因已被分离出来,其分子结构已通过对内含子-外显子边界的定位和DNA测序得以确定。该基因跨度为35kb,包含13个外显子。人类基因的结构与仓鼠天冬酰胺合成酶基因的结构高度相似,除了一个内含子区域外,其他内含子区域的位置相同。该基因的5'上游区域与其他管家基因一样,缺乏传统的TATA盒和CAAT盒。人类和仓鼠基因5'上游序列的比较显示相似性有限;然而,两者的G + C含量都非常高,这可能通过DNA甲基化在表达中发挥作用。