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PMID: 60178 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Enzymatic in vitro synthesis of globin genes.

Cell ·Vol. 7 ·No. 2 ·1976-02-00 ·Pages 279-88

Efstratiadis A, Kafatos FC, Maxam AM, Maniatis T

Abstract

Full-length, single-stranded rabbit globin cDNA, synthesized by AMV reverse transcriptase, apparently contains a small double-stranded sequence (hairpin) at the 3' terminus. This cDNA can serve as template-primer for E. coli DNA polymerase I, which synthesizes a strand complementary to the cDNA and covalently bound to it. The loop connecting the two strands can be cut by S1 nuclease. Reassociation, hybridization, and restriction endonuclease studies, as well as electrophoretic analyses, indicate that the sequential actions of reverse transcriptase, DNA polymerase 1, and S1 nuclease generate full-length, double-stranded synthetic globin genes.

MeSH Terms
Animals DNA/analysis,biosynthesis,metabolism DNA Nucleotidyltransferases/metabolism DNA Restriction Enzymes/pharmacology Deoxyribonucleases/metabolism Electrophoresis, Polyacrylamide Gel Genes Globins/biosynthesis Nucleic Acid Hybridization RNA-Directed DNA Polymerase/metabolism Rabbits
Chemicals
Globins DNA DNA Nucleotidyltransferases RNA-Directed DNA Polymerase Deoxyribonucleases DNA Restriction Enzymes
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Efstratiadis A
Kafatos F C
Maxam A M
Maniatis T
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1976-02-00
Pages
279-88
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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