Gene Expression: Chemical Synthesis and Molecular Cloning of a Bacteriophage T5 (T5P25) Early Promoter
Overview
Authors
Affiliations
A sixty base pair DNA duplex containing the nucleotide sequence of the bacteriophage T5 early (T5P25) promoter has been constructed using a combination of chemical synthesis and enzymatic methods. Subsequent to cloning into pBR322, the promoter has been demonstrated to be biologically active being capable of directing the efficient expression of genes under its control. This serves as a prototype for an approach to the study of the in vivo structure-function relationships and efficiency of promoters.
Novel RNA Polymerase Binding Protein Encoded by Bacteriophage T5.
Klimuk E, Mekler V, Lavysh D, Serebryakova M, Akulenko N, Severinov K Viruses. 2020; 12(8).
PMID: 32722583 PMC: 7472727. DOI: 10.3390/v12080807.
Design and synthesis of synthetic UP elements for modulation of gene expression in .
Presnell K, Flexer-Harrison M, Alper H Synth Syst Biotechnol. 2019; 4(2):99-106.
PMID: 31080900 PMC: 6501063. DOI: 10.1016/j.synbio.2019.04.002.
Attenuation-based dual-fluorescent-protein reporter for screening translation inhibitors.
Osterman I, Prokhorova I, Sysoev V, Boykova Y, Efremenkova O, Svetlov M Antimicrob Agents Chemother. 2012; 56(4):1774-83.
PMID: 22252829 PMC: 3318315. DOI: 10.1128/AAC.05395-11.
Chao M, Kan M, Lin-Chao S Nucleic Acids Res. 1995; 23(10):1691-5.
PMID: 7540285 PMC: 306923. DOI: 10.1093/nar/23.10.1691.
Chen H, Bjerknes M, Kumar R, Jay E Nucleic Acids Res. 1994; 22(23):4953-7.
PMID: 7528374 PMC: 523762. DOI: 10.1093/nar/22.23.4953.