Ramírez-Sánchez Irais, Magos-Castro Marco, Guarneros Gabriel
Departamento de Genética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional, Mexico City, Mexico.
Front Microbiol. 2023 Feb 3;14:1027380. doi: 10.3389/fmicb.2023.1027380. eCollection 2023.
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.
关于温和噬菌体从溶原周期向裂解周期转变过程中的基因表达程序,人们了解甚少。为了研究这个问题,我们构建了一个溶原菌中的温度敏感型阻遏物突变体,并通过链特异性RNA测序分析了热诱导前后的噬菌体转录程序。正如预期的那样,位于噬菌体DNA正链上的阻遏物基因在30°C的允许温度下于溶原菌中被转录。在阻遏物基因上游,我们注意到存在两个明显在同一转录本中的重叠开放阅读框(ORF)。一个ORF是一个基因,它编码一种7.9 kDa的蛋白质,介导对各种超感染噬菌体的排斥。另一个ORF与第一个基因的AUG下游25个核苷酸处可能的AUG起始密码子处于交替阅读框中,预计编码一种功能未知的20.7 kDa多肽。在40°C解除阻遏后,参与裂解周期的一个操纵子的转录从噬菌体DNA反链上的一个启动子开始。该操纵子中的第一个基因是抗阻遏物的同源物,是其他噬菌体裂解 - 溶原调控区域中的一个常见基因。有趣的是, 在 之后的下一个基因是基因 ,它在反链上与正链上的重叠基因 重叠。奇怪的是,基因 的表达也显示出超感染排斥。链特异性RNA测序还揭示了噬菌体裂解阶段表达的基因模块的转录顺序。具有相似功能的重叠基因的保守性可能是经过进化选择的。