Abstract
Two similarities among transcriptional activating regions of many eukaryotic transcription factors, like those from GAL4, GCN4, and VP16, are that they have a net negative charge, and that many of them can potentially form amphipathic alpha-helices with acidic amino acids on the hydrophilic face. Based on these similarities, E. Giniger and M. Ptashne previously designed a short peptide (AH) which is predicted to have the potential to form a negatively charged amphipathic alpha-helix; AH was able to mediate transcription activation in yeast when it was attached to the DNA binding and dimerization portion of GAL4 [GAL4(1-147)]. This paper describes screening of a pool of AH derivatives containing randomized amino acids fused to GAL4(1-147) and to an analogous region of LexA [LexA(1-87)] in yeast strains. Results suggest that both acidic and hydrophobic amino acids are critical features of activating regions--these results are consistent with the model that activating regions often form amphipathic alpha-helices. This work is novel because hydrophobic amino acids are also shown to be important in activating regions of yeast transcription factors.
MeSH Terms
Amino Acid Sequence
Amino Acids/metabolism
Bacterial Proteins/metabolism
Base Sequence
DNA, Fungal
DNA-Binding Proteins
Fungal Proteins/chemistry,metabolism
Molecular Sequence Data
Mutagenesis
Peptides/chemical synthesis,chemistry,metabolism
Plasmids
Prokaryotic Cells/metabolism
Protein Binding
Saccharomyces cerevisiae/genetics
Saccharomyces cerevisiae Proteins
Serine Endopeptidases
Transcription Factors/chemistry,metabolism
Chemicals
Amino Acids
Bacterial Proteins
DNA, Fungal
DNA-Binding Proteins
Fungal Proteins
GAL4 protein, S cerevisiae
LexA protein, Bacteria
Peptides
Saccharomyces cerevisiae Proteins
Transcription Factors
Serine Endopeptidases
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Ruden D M
Department of Biochemistry and Molecular Biology, Harvard University, Cambridge, MA 02138.
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