An MF alpha 1-SUC2 (alpha-factor-invertase) gene fusion for study of protein localization and gene expression in yeast - PubMed (original) (raw)
An MF alpha 1-SUC2 (alpha-factor-invertase) gene fusion for study of protein localization and gene expression in yeast
S D Emr et al. Proc Natl Acad Sci U S A. 1983 Dec.
Abstract
The peptide mating pheromone alpha-factor and the hydrolytic enzyme invertase (beta-D-fructofuranoside fructohydrolase, EC 3.2.1.26) are processed from larger precursor proteins during their secretion from yeast cells (Saccharomyces cerevisiae). An in-frame fusion of the structural genes for these two proteins was constructed by connecting the 5'-flanking region and prepro-leader portion of the coding sequence of the alpha-factor gene (MF alpha 1) to a large fragment of the invertase gene (SUC2) lacking its 5'-flanking region and the coding information for the first four amino acids of its signal sequence. Sites that have been implicated in normal proteolytic processing of the alpha-factor precursor have been retained in this construction. The chimeric gene directs synthesis of a high level of active invertase that is secreted efficiently into the periplasmic space, permitting cell growth on sucrose-containing media. This extracellular invertase appears to contain no prepro-alpha-factor sequences. The initial intracellular product is, however, a hybrid protein that can be detected either by treatment of the cells with the drug tunicamycin or by blockage of secretion in a temperature-conditional secretion-defective mutant (sec18). Therefore, prior to its efficient proteolytic removal, the alpha-factor portion of the hybrid protein apparently provides the necessary information for efficient export of the substantially larger protein invertase. Similar to MF alpha 1, the MF alpha 1-SUC2 fusion is expressed in alpha haploids at levels 65-75 times higher than in a haploids or in a/alpha diploids; also, high-level expression is eliminated in mat alpha 1 mutants but not in mat alpha 2 mutants. Unlike expression of SUC2, expression of the fusion is not affected by glucose concentration. Hence, the 5'-flanking region present in the fusion (about 950 base pairs) is sufficient to confer alpha cell-specific expression to the hybrid gene.
Similar articles
- Nucleotide sequence of the yeast SUC2 gene for invertase.
Taussig R, Carlson M. Taussig R, et al. Nucleic Acids Res. 1983 Mar 25;11(6):1943-54. doi: 10.1093/nar/11.6.1943. Nucleic Acids Res. 1983. PMID: 6300785 Free PMC article. - Regulation of alpha-factor production in Saccharomyces cerevisiae: a-factor pheromone-induced expression of the MF alpha 1 and STE13 genes.
Achstetter T. Achstetter T. Mol Cell Biol. 1989 Oct;9(10):4507-14. doi: 10.1128/mcb.9.10.4507-4514.1989. Mol Cell Biol. 1989. PMID: 2685554 Free PMC article. - Structure-activity relationships of the yeast alpha-factor.
Naider F, Becker JM. Naider F, et al. CRC Crit Rev Biochem. 1986;21(3):225-48. doi: 10.3109/10409238609113612. CRC Crit Rev Biochem. 1986. PMID: 3536301 Review. - Secretion of heterologous proteins directed by the yeast alpha-factor leader.
Brake AJ. Brake AJ. Biotechnology. 1989;13:269-80. Biotechnology. 1989. PMID: 2679928 Review. No abstract available.
Cited by
- A zinc finger protein from Candida albicans is involved in sucrose utilization.
Kelly R, Kwon-Chung KJ. Kelly R, et al. J Bacteriol. 1992 Jan;174(1):222-32. doi: 10.1128/jb.174.1.222-232.1992. J Bacteriol. 1992. PMID: 1729210 Free PMC article. - Intracellular sorting and processing of a yeast vacuolar hydrolase: proteinase A propeptide contains vacuolar targeting information.
Klionsky DJ, Banta LM, Emr SD. Klionsky DJ, et al. Mol Cell Biol. 1988 May;8(5):2105-16. doi: 10.1128/mcb.8.5.2105-2116.1988. Mol Cell Biol. 1988. PMID: 3290649 Free PMC article. - In vitro reconstitution of intercompartmental protein transport to the yeast vacuole.
Vida TA, Graham TR, Emr SD. Vida TA, et al. J Cell Biol. 1990 Dec;111(6 Pt 2):2871-84. doi: 10.1083/jcb.111.6.2871. J Cell Biol. 1990. PMID: 2269659 Free PMC article. - Processing and secretion of the Yarrowia lipolytica RNase.
Cheng SC, Ogrydziak DM. Cheng SC, et al. J Bacteriol. 1987 Apr;169(4):1433-40. doi: 10.1128/jb.169.4.1433-1440.1987. J Bacteriol. 1987. PMID: 3549686 Free PMC article. - Localization of components involved in protein transport and processing through the yeast Golgi apparatus.
Franzusoff A, Redding K, Crosby J, Fuller RS, Schekman R. Franzusoff A, et al. J Cell Biol. 1991 Jan;112(1):27-37. doi: 10.1083/jcb.112.1.27. J Cell Biol. 1991. PMID: 1986005 Free PMC article.
References
- Cell. 1983 Feb;32(2):409-15 - PubMed
- Cell. 1983 Mar;32(3):839-52 - PubMed
- Nucleic Acids Res. 1983 Mar 25;11(6):1943-54 - PubMed
- Mol Cell Biol. 1983 Mar;3(3):439-47 - PubMed
- J Bacteriol. 1983 Aug;155(2):903-6 - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases