TY - JOUR
T1 - Effect of mutations in the cII and cIII genes of bacteriophage λ on macromolecular synthesis in infected cells
AU - McMacken, R.
AU - Mantei, N.
AU - Butler, B.
AU - Joyner, A.
AU - Echols, H.
N1 - Funding Information:
We thank Roy Gingery. Mark Willard and Linda Pilarski for assistancein obtaining the [sH]thymidine incorporation data shown in Fig. 3. We are grateful to Julius Adler, Werner Arber, William Dove, Joseph Ferreti, A. D. Kaiser, Margaret Lieb and Ethan Signer for the donation of bacterial strains and phage. In addition, the helpful advice of Dr Dove regarding the serum blocking power assay technique is greatly appreciated. The research was supported in part by U.S. Public Health Service research grants GMO8407, GM09570 and GM17078, and U.S. Public Health Service training grant GMO0236. One of us (R. M.) is a National Aeronautics and Space Administration Trainee, and one of us (N. M.) is a National Science Foundation pm-doctoral fellow.
PY - 1970/5/14
Y1 - 1970/5/14
N2 - We have investigated the time-course of macromolecular synthesis following infection by cI-, cII- and cIII- mutants of λ in an effort to understand the role of the cII and cIII genes in the establishment of repression and lysogeny. cII- and cIII- mutants of λ begin to synthesize the "late" proteins tail antigen and lysozyme substantially before a cI- mutant; the shift to late messenger RNA production from the head and tail genes also occurs earlier after cII- or cIII- infection. In contrast, no appreciable difference among cI-, cII-, or cIII- mutants was found in synthesis of the "early" protein λ-exonuclease or in the rate of total or λ-specific DNA synthesis. These results suggest that the λ cII and cIII gene products function to delay the lytic response by inhibiting, directly or indirectly, the production of messenger RNA from the late λ genes. When lysozyme synthesis was studied after infection by cI- cII- and cI- cIII- double mutants, results were obtained which were similar to those found in the case of single cII- and cIII- mutants. The results with the double mutants suggest that the cII and cIII gene products may also participate in the regulation of cI represser synthesis or activity.
AB - We have investigated the time-course of macromolecular synthesis following infection by cI-, cII- and cIII- mutants of λ in an effort to understand the role of the cII and cIII genes in the establishment of repression and lysogeny. cII- and cIII- mutants of λ begin to synthesize the "late" proteins tail antigen and lysozyme substantially before a cI- mutant; the shift to late messenger RNA production from the head and tail genes also occurs earlier after cII- or cIII- infection. In contrast, no appreciable difference among cI-, cII-, or cIII- mutants was found in synthesis of the "early" protein λ-exonuclease or in the rate of total or λ-specific DNA synthesis. These results suggest that the λ cII and cIII gene products function to delay the lytic response by inhibiting, directly or indirectly, the production of messenger RNA from the late λ genes. When lysozyme synthesis was studied after infection by cI- cII- and cI- cIII- double mutants, results were obtained which were similar to those found in the case of single cII- and cIII- mutants. The results with the double mutants suggest that the cII and cIII gene products may also participate in the regulation of cI represser synthesis or activity.
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U2 - 10.1016/0022-2836(70)90288-3
DO - 10.1016/0022-2836(70)90288-3
M3 - Article
C2 - 5453348
AN - SCOPUS:0014944975
SN - 0022-2836
VL - 49
SP - 639
EP - 655
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 3
ER -