» Articles » PMID: 2668117

Amino Acid Sequence Similarity Between GCN3 and GCD2, Positive and Negative Translational Regulators of GCN4: Evidence for Antagonism by Competition

Overview
Journal Genetics
Specialty Genetics
Date 1989 Jul 1
PMID 2668117
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

The GCD2 gene product is required in conditions of amino acid sufficiency to repress the synthesis of GCN4, a transcriptional activator of amino acid biosynthetic genes in Saccharomyces cerevisiae. GCD2 is also required unconditionally for cell viability. The constitutive derepression of GCN4 expression and temperature sensitivity for growth associated with GCD2 alleles, known as gcd12 mutations, are completely masked by wild-type GCN3, a positive regulator of GCN4 expression. This observation suggests that GCN3 can promote or at least partially substitute for GCD2 function in normal growth conditions, while acting as an antagonist of GCD2 in amino acid starvation conditions. We report here that the predicted amino acid sequence of GCN3 shows extensive similarity with the carboxyl-terminal portion of GCD2. Based on this finding, it seems likely that gcd12 mutations specifically affect the domain of GCD2 that is similar in sequence to GCN3. We propose that GCN3 can substitute for this domain in a gcd12 mutant grown in normal growth conditions, and that modification of GCN3 in starvation conditions causes it to interfere with, rather than substitute for GCD2 function. A gcd2 deletion and gcd2-1 are each expected to inactivate a second domain for which GCN3 cannot substitute, accounting for the inability of GCN3 to mask the phenotypes associated with these mutations.

Citing Articles

Identification of residues that underpin interactions within the eukaryotic initiation factor (eIF2) 2B complex.

Wang X, Wortham N, Liu R, Proud C J Biol Chem. 2012; 287(11):8263-74.

PMID: 22238342 PMC: 3318736. DOI: 10.1074/jbc.M111.331553.


Minimum requirements for the function of eukaryotic translation initiation factor 2.

Erickson F, Nika J, Rippel S, Hannig E Genetics. 2001; 158(1):123-32.

PMID: 11333223 PMC: 1461651. DOI: 10.1093/genetics/158.1.123.


eIF2 independently binds two distinct eIF2B subcomplexes that catalyze and regulate guanine-nucleotide exchange.

Pavitt G, Ramaiah K, Kimball S, Hinnebusch A Genes Dev. 1998; 12(4):514-26.

PMID: 9472020 PMC: 316533. DOI: 10.1101/gad.12.4.514.


eIF2B, the guanine nucleotide-exchange factor for eukaryotic initiation factor 2. Sequence conservation between the alpha, beta and delta subunits of eIF2B from mammals and yeast.

Price N, Mellor H, Craddock B, Flowers K, Kimball S, Wilmer T Biochem J. 1996; 318 ( Pt 2):637-43.

PMID: 8929216 PMC: 1217679. DOI: 10.1042/bj3180637.


Identification of a regulatory subcomplex in the guanine nucleotide exchange factor eIF2B that mediates inhibition by phosphorylated eIF2.

Yang W, Hinnebusch A Mol Cell Biol. 1996; 16(11):6603-16.

PMID: 8887689 PMC: 231662. DOI: 10.1128/MCB.16.11.6603.


References
1.
Dever T, Glynias M, Merrick W . GTP-binding domain: three consensus sequence elements with distinct spacing. Proc Natl Acad Sci U S A. 1987; 84(7):1814-8. PMC: 304531. DOI: 10.1073/pnas.84.7.1814. View

2.
Fry D, KUBY S, Mildvan A . ATP-binding site of adenylate kinase: mechanistic implications of its homology with ras-encoded p21, F1-ATPase, and other nucleotide-binding proteins. Proc Natl Acad Sci U S A. 1986; 83(4):907-11. PMC: 322979. DOI: 10.1073/pnas.83.4.907. View

3.
Harashima S, Hannig E, Hinnebusch A . Interactions between positive and negative regulators of GCN4 controlling gene expression and entry into the yeast cell cycle. Genetics. 1987; 117(3):409-19. PMC: 1203217. DOI: 10.1093/genetics/117.3.409. View

4.
Hinnebusch A . Mechanisms of gene regulation in the general control of amino acid biosynthesis in Saccharomyces cerevisiae. Microbiol Rev. 1988; 52(2):248-73. PMC: 373138. DOI: 10.1128/mr.52.2.248-273.1988. View

5.
Hannig E, Hinnebusch A . Molecular analysis of GCN3, a translational activator of GCN4: evidence for posttranslational control of GCN3 regulatory function. Mol Cell Biol. 1988; 8(11):4808-20. PMC: 365574. DOI: 10.1128/mcb.8.11.4808-4820.1988. View