Cunningham T S, Dorrington R A, Cooper T G
Department of Microbiology and Immunology, University of Tennessee, Memphis 38163.
J Bacteriol. 1994 Aug;176(15):4718-25. doi: 10.1128/jb.176.15.4718-4725.1994.
Expression of the nitrogen catabolic genes in Saccharomyces cerevisiae, including those of the gamma-aminobutyric acid (UGA) and allantoin (DAL) pathways, is regulated positively by the GLN3 protein and negatively by the DAL80 protein. The deduced sequences of the DAL80 and GLN3 proteins contain a zinc finger motif homologous to those shown to bind GATA sequences. In addition, DAL80 protein has been directly shown to bind to a pair of GATA-containing sequences (URSGATA) in vitro, and a pair of GATA-containing sequences (UASNTR) is required for GLN3-dependent transcriptional activation in a heterologous expression vector. We demonstrate here that the GATA-containing sites upstream of UGA4 required for optimal GLN3-dependent transcriptional activation also mediate DAL80 protein binding in vitro and DAL80-responsive regulation in vivo.
酿酒酵母中氮分解代谢基因的表达,包括γ-氨基丁酸(UGA)和尿囊素(DAL)途径的那些基因,受到GLN3蛋白的正向调控和DAL80蛋白的负向调控。DAL80和GLN3蛋白的推导序列含有一个锌指基序,该基序与那些已显示能结合GATA序列的锌指基序同源。此外,已直接证明DAL80蛋白在体外能与一对含GATA的序列(URSGATA)结合,并且在异源表达载体中,一对含GATA的序列(UASNTR)是GLN3依赖性转录激活所必需的。我们在此证明,UGA4上游对于最佳GLN3依赖性转录激活所必需的含GATA位点,在体外也介导DAL80蛋白结合以及在体内介导DAL80反应性调控。