Abstract
A yeast transcriptional activator, Gcn4p, induces the expression of genes that are involved in amino acid and purine biosynthetic pathways under amino acid starvation. Gcn4p has an acidic activation domain in the central region and a bZIP domain in the C-terminus that is divided into the DNA-binding motif and dimerization leucine zipper motif. In order to identify amino acids in the DNA-binding motif of Gcn4p which are involved in transcriptional activation, we constructed mutant libraries in the DNA-binding motif through an innovative application of random mutagenesis. Mutant library made by oligonucleotides which were mutated randomly using the Poisson distribution showed that the actual mutation frequency was in good agreement with expected values. This method could save the time and effort to create a mutant library with a predictable mutation frequency. Based on the studies using the mutant libraries constructed by the new method, the specific residues of the DNA-binding domain in Gcn4p appear to be involved in the transcriptional activities on a conserved binding site.
Original language | English |
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Pages (from-to) | 442-450 |
Number of pages | 9 |
Journal | Journal of Microbiological Methods |
Volume | 69 |
Issue number | 3 |
DOIs | |
Publication status | Published - 2007 Jun |
Bibliographical note
Funding Information:This work was supported in part by FPR05C2-390 of 21C Frontier Functional Proteomics Project from the Korean Ministry of Science and Technology.
Keywords
- Gcn4p
- Poisson distribution
- Random mutagenesis
- bZIP transcriptional factor
ASJC Scopus subject areas
- Microbiology
- Molecular Biology
- Microbiology (medical)