Nucleic Acids Research, 1988, Vol. 16, No. 3 1011-1026
© 1988
Articles |
N4 virion DNA dependent-RNA polymerase: initiation sequences utilized by the enzyme on heterologous templates
Departments of Molecular Genetics and Cell Biology and Department of Biochemistiy and Molecular Biology, University of Chicago 920 East 58th St., Chicago, IL 60637, USA
+To whom correspondence should be addressed
Received September 24, 1987. Accepted December 14, 1987.
Bacteriophage N4 virion-encapaulated RNA polymerase, the enzyme responaible for transcription of the phage early RNAs, is unable to use duplex linear DNA as a template. In contrast to other RNA polymerases, the enzyme transcribes denatured N4 DNA with in vivo specificity. The promoter sequences for three sites of transcription initiation on the N4 genome have been determined and found to contain conserved sequences and two sets of inverted repeats. In order to define the minimal sequence requirements for N4 virion RNA polymerase activity, we have screened several heterologoua DNAs, amounting to 64,328 bases, for their ability to support transcription. Several sequences allowing specific initiation were found. Their location, properties and the relation to N4 virion RNA polymerase promoters are discussed.
*Present address: Department of Viral Biology, USAMRIID, Fort Dietrick, Frederick, MD, USA