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Mol Cell Biol. 1992 Sep;12(9):3834-42. doi: 10.1128/mcb.12.9.3834-3842.1992.
2
The E-box DNA binding protein Sgc1p suppresses the gcr2 mutation, which is involved in transcriptional activation of glycolytic genes in Saccharomyces cerevisiae.E-box DNA结合蛋白Sgc1p可抑制gcr2突变,该突变与酿酒酵母中糖酵解基因的转录激活有关。
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本文引用的文献

1
Codon selection in yeast.酵母中的密码子选择
J Biol Chem. 1982 Mar 25;257(6):3026-31.
2
The gcr (glycolysis regulation) mutation of Saccharomyces cerevisiae.酿酒酵母的gcr(糖酵解调节)突变
J Biol Chem. 1981 Dec 25;256(24):13074-8.
3
Studies on transformation of Escherichia coli with plasmids.大肠杆菌质粒转化的研究。
J Mol Biol. 1983 Jun 5;166(4):557-80. doi: 10.1016/s0022-2836(83)80284-8.
4
Transformation of intact yeast cells treated with alkali cations.经碱金属阳离子处理的完整酵母细胞的转化
J Bacteriol. 1983 Jan;153(1):163-8. doi: 10.1128/jb.153.1.163-168.1983.
5
Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis.利用寡脱氧核苷酸定向诱变构建改良的M13载体。
Gene. 1983 Dec;26(1):101-6. doi: 10.1016/0378-1119(83)90040-9.
6
Cloning of yeast glycolysis genes by complementation.通过互补作用克隆酵母糖酵解基因。
Biochem Biophys Res Commun. 1982 Oct 15;108(3):1107-22. doi: 10.1016/0006-291x(82)92114-3.
7
A short amino acid sequence able to specify nuclear location.一段能够指定核定位的短氨基酸序列。
Cell. 1984 Dec;39(3 Pt 2):499-509. doi: 10.1016/0092-8674(84)90457-4.
8
Sequence requirements for nuclear location of simian virus 40 large-T antigen.猿猴病毒40大T抗原核定位的序列要求。
Nature. 1984;311(5981):33-8. doi: 10.1038/311033a0.
9
Cooperation of glycolytic enzymes.糖酵解酶的协同作用。
Adv Enzyme Regul. 1969;7:149-67. doi: 10.1016/0065-2571(69)90016-8.
10
The GCR1 gene encodes a positive transcriptional regulator of the enolase and glyceraldehyde-3-phosphate dehydrogenase gene families in Saccharomyces cerevisiae.GCR1基因编码酿酒酵母中烯醇酶和甘油醛-3-磷酸脱氢酶基因家族的一个正向转录调节因子。
Mol Cell Biol. 1987 Feb;7(2):813-20. doi: 10.1128/mcb.7.2.813-820.1987.

GCR2在酵母糖酵解基因转录激活中的作用。

Role of GCR2 in transcriptional activation of yeast glycolytic genes.

作者信息

Uemura H, Jigami Y

机构信息

Division of Biological Chemistry, Tsukuba Research Center (MITI), Ibaraki, Japan.

出版信息

Mol Cell Biol. 1992 Sep;12(9):3834-42. doi: 10.1128/mcb.12.9.3834-3842.1992.

DOI:10.1128/mcb.12.9.3834-3842.1992
PMID:1508187
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC360254/
Abstract

The Saccharomyces cerevisiae GCR2 gene affects expression of most of the glycolytic genes. We report the nucleotide sequence of GCR2, which can potentially encode a 58,061-Da protein. There is a small cluster of asparagines near the center and a C-terminal region that would be highly charged but overall neutral. Fairly homologous regions were found between Gcr2 and Gcr1 proteins. To test potential interactions, the genetic method of S. Fields and O. Song (Nature [London] 340:245-246, 1989), which uses protein fusions of candidate gene products with, respectively, the N-terminal DNA-binding domain of Gal4 and the C-terminal activation domain II, assessing restoration of Gal4 function, was used. In a delta gal4 delta gal80 strain, double transformation by plasmids containing, respectively, a Gal4 (transcription-activating region)/Gcr1 fusion and a Gal4 (DNA-binding domain)/Gcr2 fusion activated lacZ expression from an integrated GAL1/lacZ fusion, indicating reconstitution of functional Gal4 through the interaction of Gcr1 and Gcr2 proteins. The Gal4 (transcription-activating region)/Gcr1 fusion protein alone complemented the defects of both gcr1 and gcr2 strains. Furthermore, a Rap1/Gcr2 fusion protein partially complemented the defects of gcr1 strains. These results suggest that Gcr2 has transcriptional activation activity and that the GCR1 and GCR2 gene products function together.

摘要

酿酒酵母GCR2基因影响大多数糖酵解基因的表达。我们报道了GCR2的核苷酸序列,它可能编码一种58,061道尔顿的蛋白质。在中心附近有一小簇天冬酰胺,还有一个C端区域,该区域电荷较高但总体呈中性。在Gcr2和Gcr1蛋白之间发现了相当同源的区域。为了测试潜在的相互作用,采用了S. Fields和O. Song(《自然》[伦敦]340:245 - 246,1989年)的遗传方法,该方法使用候选基因产物分别与Gal4的N端DNA结合结构域和C端激活结构域II的蛋白质融合体,评估Gal4功能的恢复情况。在Δgal4Δgal80菌株中,分别含有Gal4(转录激活区域)/Gcr1融合体和Gal4(DNA结合结构域)/Gcr2融合体的质粒进行双转化,激活了整合的GAL1/lacZ融合体的lacZ表达,表明通过Gcr1和Gcr2蛋白的相互作用重建了功能性Gal4。单独的Gal4(转录激活区域)/Gcr1融合蛋白弥补了gcr1和gcr2菌株的缺陷。此外,Rap1/Gcr2融合蛋白部分弥补了gcr1菌株的缺陷。这些结果表明Gcr2具有转录激活活性,并且GCR1和GCR2基因产物共同发挥作用。