Gene expression: chemical synthesis and molecular cloning of a bacteriophage T5 (T5P25) early promoter.

Abstract:

: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.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Rommens J,MacKnight D,Pomeroy-Cloney L,Jay E

doi

10.1093/nar/11.17.5921

subject

Has Abstract

pub_date

1983-09-10 00:00:00

pages

5921-40

issue

17

eissn

0305-1048

issn

1362-4962

journal_volume

11

pub_type

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