SEQUENCE AND EXPRESSION OF GLN3, A POSITIVE NITROGEN REGULATORY GENE OF SACCHAROMYCES-CEREVISIAE ENCODING A PROTEIN WITH A PUTATIVE ZINC FINGER DNA-BINDING DOMAIN

被引:175
作者
MINEHART, PL [1 ]
MAGASANIK, B [1 ]
机构
[1] MIT, DEPT BIOL, CAMBRIDGE, MA 02139 USA
关键词
D O I
10.1128/MCB.11.12.6216
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The GLN3 gene of Saccharomyces cerevisiae is required for the activation of transcription of a number of genes in response to the replacement of glutamine by glutamate as source of nitrogen. We cloned the GLN3 gene and constructed null alleles by gene disruption. GLN3 is not essential for growth, but increased copies of GLN3 lead to a drastic decrease in growth rate. The complete nucleotide sequence of the GLN3 gene was determined, revealing one open reading frame encoding a polypeptide of 730 amino acids, with a molecular weight of approximately 80,000. The GLN3 protein contains a single putative Cys2/Cys2 zinc finger which has homology to the Neurospora crassa NIT2 protein, the Aspergillus nidulans AREA protein, and the erythroid-specific transcription factor GATA-1. Immunoprecipitation experiments indicated that the GLN3 protein binds the nitrogen upstream activation sequence of GLN1, the gene encoding glutamine synthetase. Neither control of transcription nor control of initiation of translation of GLN3 is important for regulation in response to glutamine availability.
引用
收藏
页码:6216 / 6228
页数:13
相关论文
共 60 条
[1]
3 REGULATORY SYSTEMS CONTROL EXPRESSION OF GLUTAMINE-SYNTHETASE IN SACCHAROMYCES-CEREVISIAE AT THE LEVEL OF TRANSCRIPTION [J].
BENJAMIN, PM ;
WU, JL ;
MITCHELL, AP ;
MAGASANIK, B .
MOLECULAR & GENERAL GENETICS, 1989, 217 (2-3) :370-377
[2]
CONSTRUCTION AND CHARACTERIZATION OF NEW CLONING VEHICLES .2. MULTIPURPOSE CLONING SYSTEM [J].
BOLIVAR, F ;
RODRIGUEZ, RL ;
GREENE, PJ ;
BETLACH, MC ;
HEYNEKER, HL ;
BOYER, HW ;
CROSA, JH ;
FALKOW, S .
GENE, 1977, 2 (02) :95-113
[3]
STERILE HOST YEASTS (SHY) - EUKARYOTIC SYSTEM OF BIOLOGICAL CONTAINMENT FOR RECOMBINANT DNA EXPERIMENTS [J].
BOTSTEIN, D ;
FALCO, SC ;
STEWART, SE ;
BRENNAN, M ;
SCHERER, S ;
STINCHCOMB, DT ;
STRUHL, K ;
DAVIS, RW .
GENE, 1979, 8 (01) :17-24
[4]
2 DIFFERENTIALLY REGULATED MESSENGER-RNAS WITH DIFFERENT 5' ENDS ENCODE SECRETED AND INTRACELLULAR FORMS OF YEAST INVERTASE [J].
CARLSON, M ;
BOTSTEIN, D .
CELL, 1982, 28 (01) :145-154
[5]
THE SPT6 GENE IS ESSENTIAL FOR GROWTH AND IS REQUIRED FOR DELTA-MEDIATED TRANSCRIPTION IN SACCHAROMYCES-CEREVISIAE [J].
CLARKADAMS, CD ;
WINSTON, F .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (02) :679-686
[6]
THE GLN3 GENE-PRODUCT IS REQUIRED FOR TRANSCRIPTIONAL ACTIVATION OF ALLANTOIN SYSTEM GENE-EXPRESSION IN SACCHAROMYCES-CEREVISIAE [J].
COOPER, TG ;
FERGUSON, D ;
RAI, R ;
BYSANI, N .
JOURNAL OF BACTERIOLOGY, 1990, 172 (02) :1014-1018
[7]
Cooper TG, 1982, MOL BIOL YEAST SACCH, P39, DOI DOI 10.1101/087969180.11B.39
[8]
THE URE2 GENE-PRODUCT OF SACCHAROMYCES-CEREVISIAE PLAYS AN IMPORTANT ROLE IN THE CELLULAR-RESPONSE TO THE NITROGEN-SOURCE AND HAS HOMOLOGY TO GLUTATHIONE S-TRANSFERASES [J].
COSCHIGANO, PW ;
MAGASANIK, B .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (02) :822-832
[9]
PHYSIOLOGICAL AND GENETIC-ANALYSIS OF THE CARBON REGULATION OF THE NAD-DEPENDENT GLUTAMATE-DEHYDROGENASE OF SACCHAROMYCES-CEREVISIAE [J].
COSCHIGANO, PW ;
MILLER, SM ;
MAGASANIK, B .
MOLECULAR AND CELLULAR BIOLOGY, 1991, 11 (09) :4455-4465
[10]
REGULATION OF NITROGEN ASSIMILATION IN SACCHAROMYCES-CEREVISIAE - ROLES OF THE URE2 AND GLN3 GENES [J].
COURCHESNE, WE ;
MAGASANIK, B .
JOURNAL OF BACTERIOLOGY, 1988, 170 (02) :708-713