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PMID: 6310493 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

A comparison of the promoter strengths of two eukaryotic genes in vitro reveals a region of DNA that can influence the rate of transcription in cis over long distances.

Nucleic acids research ·Vol. 11 ·No. 16 ·1983-08-25 ·Pages 5317-26

Gregory SP, Butterworth PH

Abstract

We have compared the strength of a trout protamine gene promoter with that of the mouse beta major-globin gene by analysing the relative levels of run-off transcripts produced in a single mammalian in vitro transcription reaction. When the promoters are introduced on separate recombinant plasmids, the protamine transcripts are synthesised with much greater efficiency than those originating from the globin cap site. This enhanced transcription of the protamine gene is again observed when the promoters are applied as separate DNA fragments derived from the same recombinant plasmid. However, when the promoters are linked on a DNA fragment that includes 7 kb of DNA separating the initiation sites, then there is a marked reduction in the protamine signal relative to the globin. Deletion of a region of this fragment that contains the sequences flanking the globin gene at positions -335 to -1400 restores the enhanced protamine gene expression to the levels observed when the promoters are carried on separate DNA fragments.

MeSH Terms
Animals Base Sequence DNA Restriction Enzymes DNA, Recombinant/metabolism Genes Globins/genetics Mice Nucleic Acid Hybridization Operon Protamines/genetics Species Specificity Transcription, Genetic Trout
Chemicals
DNA, Recombinant Protamines Globins DNA Restriction Enzymes
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gregory S P
Butterworth P H
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22 references, click to expand
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Article Info
Journal
Nucleic acids research
Abbr.
Nucleic Acids Res
ISSN
0305-1048
Published
1983-08-25
Pages
5317-26
Language
English
Region
England
NLM ID
0411011
PMCID
PMC326280
Subset
IM
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