Lee H, Fu Y H, Marzluf G A
Department of Biochemistry, Ohio State University, Columbus 43210.
Biochemistry. 1990 Sep 18;29(37):8779-87. doi: 10.1021/bi00489a039.
The nitrogen regulatory circuit of Neurospora crassa contains structural genes that encode nitrogen catabolic enzymes which are subject to complex genetic and metabolic regulation. This set of genes is controlled by nitrogen limitation, by specific induction, and by the action of nit-2, a major positive-acting regulatory gene, and nmr, a negative-acting control gene. The complete nucleotide sequence of alc, the gene that encodes allantoicase, a purine catabolic enzyme, is presented. The alc gene contains a single intron, is transcribed from two initiation sites situated approximately 50 nb upstream of the translation start site, and encodes a protein comprised of 354 amino acids. Mobility shift and DNA footprint experiments identified a single binding site for the NIT2 regulatory protein in the alc promoter region. The binding site contains a 10 nucleotide base pair symmetrical sequence which is flanked by two possible core binding sequences, TATCT and TATCG. Mutant NIT2/beta-gal fusion proteins with amino acid substitutions in a putative zinc-finger motif were shown to be completely deficient in the ability to bind to the alc promoter DNA fragment.
粗糙脉孢菌的氮调节回路包含编码氮分解代谢酶的结构基因,这些基因受到复杂的遗传和代谢调控。这组基因受氮限制、特定诱导以及主要的正调控基因nit-2和负调控基因nmr的作用控制。本文给出了编码嘌呤分解代谢酶尿囊酸酶的基因alc的完整核苷酸序列。alc基因含有一个内含子,从位于翻译起始位点上游约50个核苷酸处的两个起始位点转录,编码一个由354个氨基酸组成的蛋白质。迁移率变动和DNA足迹实验确定了alc启动子区域中NIT2调节蛋白的一个单一结合位点。该结合位点包含一个10个核苷酸对的对称序列,两侧是两个可能的核心结合序列TATCT和TATCG。在假定的锌指基序中具有氨基酸取代的突变型NIT2/β-半乳糖苷酶融合蛋白被证明完全缺乏与alc启动子DNA片段结合的能力。