» Articles » PMID: 36819063

Transcriptional Analysis in Bacteriophage Fc02 of Revealed Two Overlapping Genes with Exclusion Activity

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2023 Feb 23
PMID 36819063
Authors
Affiliations
Soon will be listed here.
Abstract

Little is known about the gene expression program during the transition from lysogenic to lytic cycles of temperate bacteriophages in . To investigate this issue, we developed a thermo-sensitive repressor mutant in a lysogen and analyzed the phage transcriptional program by strand-specific RNA-Seq before and after thermo-induction. As expected, the repressor gene located on the phage DNA forward strand is transcribed in the lysogen at the permissive temperature of 30°C. Upstream the repressor gene, we noticed the presence of two overlapped ORFs apparently in the same transcript. One ORF is a gene that encodes a protein of 7.9 kDa mediating the exclusion of various super-infecting phages. The other ORF, placed in an alternate reading frame with a possible AUG initiation codon at 25 nucleotide downstream of the AUG of the first gene, is expected to encode a 20.7 kDa polypeptide of yet an unknown function. Upon lifting repression at 40°C, the transcription of an operon which is involved in the lytic cycle is started from a promoter on the reverse phage DNA strand. The first gene in the operon is a homolog of the antirepresor , a common gene in the lysis-lysogeny regulation region of other phages. Interestingly, the next gene after is gene that on the reverse strand overlaps the overlapped gene on the forward strand. Curiously, gene expression also shows superinfection exclusion. Strand-specific RNA-Seq also has uncovered the transcription succession of gene modules expressed during the phage lytic stage. The conservation of overlapped genes with similar functions may be evolutionarily selected.

References
1.
Coppens L, Lavigne R . SAPPHIRE: a neural network based classifier for σ70 promoter prediction in Pseudomonas. BMC Bioinformatics. 2020; 21(1):415. PMC: 7510298. DOI: 10.1186/s12859-020-03730-z. View

2.
Wu H, Zhang Y, Jiang Y, Wu H, Sun W, Huang Y . Characterization and Genomic Analysis of ɸSHP3, a New Transposable Bacteriophage Infecting Stenotrophomonas maltophilia. J Virol. 2021; 95(9). PMC: 8104090. DOI: 10.1128/JVI.00019-21. View

3.
Aparicio T, Jensen S, Nielsen A, de Lorenzo V, Martinez-Garcia E . The Ssr protein (T1E_1405) from Pseudomonas putida DOT-T1E enables oligonucleotide-based recombineering in platform strain P. putida EM42. Biotechnol J. 2016; 11(10):1309-1319. DOI: 10.1002/biot.201600317. View

4.
Naville M, Ghuillot-Gaudeffroy A, Marchais A, Gautheret D . ARNold: a web tool for the prediction of Rho-independent transcription terminators. RNA Biol. 2011; 8(1):11-3. DOI: 10.4161/rna.8.1.13346. View

5.
VOGEL J, Li Z, Howe M, Toussaint A, Higgins N . Temperature-sensitive mutations in the bacteriophage Mu c repressor locate a 63-amino-acid DNA-binding domain. J Bacteriol. 1991; 173(20):6568-77. PMC: 208994. DOI: 10.1128/jb.173.20.6568-6577.1991. View