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PMID: 2157024 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S.

Genetic studies of the lac repressor. XIII. Extensive amino acid replacements generated by the use of natural and synthetic nonsense suppressors.

Journal of molecular biology ·Vol. 212 ·No. 2 ·1990-03-20 ·Pages 295-318

Kleina LG, Miller JH

Abstract

We have altered the amino acid sequence of the lac repressor one residue at a time by utilizing a collection of nonsense suppressors that permit the insertion of 13 different amino acids in response to the amber (UAG) codon, as well as an additional amino acid in response to the UGA codon. We used this collection to suppress nonsense mutations at 141 positions in the lacI gene, which encodes the 360 amino acid long lac repressor, including 53 new nonsense mutations which we constructed by oligonucleotide-directed mutagenesis. This method has generated over 1600 single amino acid substitutions in the lac repressor. We have cataloged the effects of these replacements and have interpreted the results with the objective of gaining a better understanding of lac repressor structure, and protein structure in general. The DNA binding domain of the repressor, involving the amino-terminal 59 amino acids, is extremely sensitive to substitution, with 70% of the replacements resulting in the I- phenotype. However, the remaining 301 amino acid core of the repressor is strikingly tolerant of substitutions, with only 30% of the amino acids introduced causing the I- phenotype. This analysis reveals the location of sites in the protein involved in inducer binding, tighter binding to operator and thermal stability, and permits a virtual genetic image reconstruction of the lac repressor protein.

MeSH Terms
Amino Acid Sequence Base Sequence DNA Transposable Elements Molecular Sequence Data Mutation Phenotype Repressor Proteins/genetics Suppression, Genetic Transcription Factors/genetics
Chemicals
DNA Transposable Elements Repressor Proteins Transcription Factors
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kleina L G
Molecular Biology Institute, University of California, Los Angeles 90024.
Miller J H
Article Info
Journal
Journal of molecular biology
Abbr.
J Mol Biol
ISSN
0022-2836
Published
1990-03-20
Pages
295-318
Language
English
Region
England
NLM ID
2985088R
Subset
IM
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