Function of DNA polymerase I in RNA-primed synthesis of bacteriophage M-13 duplex DNA.
AUTOR(ES)
Schneck, P K
RESUMO
Cell-free extracts from Escherichia coli contain a DNA polymerase activity resistant to SH-blocking agents, which is capable of synthesizing complementary strand DNA on a circular M-13 DNA template by extension of RNA primers. This activity is considered to be identical with DNA polymerase I (or some altered form of this enzyme) since it is missing in extracts from po1A- cells. DNA synthesis in the presence of SH-blocking agents occurs at a reduced rate as compared to untreated controls and leads to the formation of DNA chains of defined size (0.4-0.5 genome's length). It is concluded that efficient M-13 duplex DNA synthesis requires the cooperation of both DNA polymerase I and III.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=342927Documentos Relacionados
- RNA-Primed DNA Synthesis In Vitro
- Initiation of RNA-primed DNA synthesis in vitro by DNA polymerase alpha-primase.
- RNA-primed DNA synthesis: specific catalysis by HeLa cell DNA polymerase alpha.
- A cell-free system for the replication fo bacteriophage M-13 duplex DNA.
- RNA-primed initiation sites of DNA replication in the origin region of bacteriophage lambda genome.