Affiliation:
1. Department of Radiation Biology and Biophysics, and Department of Biology, University of Rochester, Rochester, New York 14620
Abstract
Mutants in T4 genes 46 and 47 exhibit early cessation of deoxyribonucleic acid (DNA) synthesis (“DNA arrest”) and decreased synthesis of late proteins and phage. In addition, mutants in genes 46 and 47 fail to degrade host DNA to acidsoluble products. It is shown here that this complex phenotype can be partially suppressed by mutation of a T4 gene external to genes 46 and 47 which has been named
das
for “
D
NA
a
rrest
s
uppressor.” The
das
mutations were discovered as third-site mutations in spontaneous pseudorevertants of [46, 47] mutants; the pseudorevertants make small plaques on
Escherichia coli
B, whereas [46, 47] mutants make none. The [
das
, 46, 47] triple mutant exhibits increased DNA, late protein, and viable phage production compared to the double mutant [46, 47]. The [
das
, 46, 47] mutant also degrades more of the host DNA to acid-soluble products than does the [46, 47] mutant. The suppressor effect of the
das
mutation appears to be gene-specific: it suppresses both
amber
and temperature-sensitive mutations in genes 46 and 47 and does not suppress
amber
mutations in any of the other genes tested. The [
das
] single mutants make normal-sized plaques on
E. coli
B and exhibit nearly normal host DNA degradation, DNA synthesis, late protein synthesis, and viable phage production. The
das
mutations either define a new gene between genes 33 and 34 or are special mutations within gene 33.
Publisher
American Society for Microbiology
Subject
Virology,Insect Science,Immunology,Microbiology
Cited by
37 articles.
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