Ventura Marco, Foley Sophie, Bruttin Anne, Chennoufi Sandra Chibani, Canchaya Carlos, Brüssow Harald
Nestlé Research Center, Nestec Ltd., Vers-chez-les-Blanc, Lausanne 26, CH-1000, Switzerland.
Virology. 2002 Apr 25;296(1):62-76. doi: 10.1006/viro.2001.1331.
For the lytic growth cycle of the temperate cos-site Streptococcus thermophilus phage Sfi21 a transcription map was developed on the basis of systematic Northern blot hybridizations. All deduced 5' ends were confirmed by primer extension analysis. Three time classes of transcripts were observed. Early transcripts were identified in four different genome regions. One prominent early mRNA of 4.8 kb length covered a group of 12 genes located between the origin of replication and the cos-site. Two short early mRNAs represented a single gene from the direct vicinity of the cos-site and the superinfection immunity gene from the lysogeny module, respectively. A fourth early transcript covered a group of four genes located between the lysin and the integrase gene. Middle transcripts of 2.1 and 5.8 kb length covered cro-like and ant-like repressor genes and the DNA replication module, respectively. Four types of late transcripts were identified. The transcripts covered the likely DNA packaging genes, the head morphogenesis module plus the major tail gene, the remainder of the tail genes, and the putative tail fiber plus lysis genes, respectively. Only the transcript from the head morphogenesis genes yielded defined late mRNA species. The transcription map concurred with most of the in silico predictions for the genome organization of phage Sfi21 except for the separation of the DNA replication module from a possible transcription regulation module. Most 5' ends of the transcripts determined in primer-extension experiments were not preceded by a consensus promoter sequence. The involvement of phage-encoded regulators for middle and late transcription was suggested by chloramphenicol-inhibition experiments.
对于温和型cos位点嗜热链球菌噬菌体Sfi21的裂解生长周期,基于系统的Northern印迹杂交构建了转录图谱。所有推导的5'端均通过引物延伸分析得到证实。观察到三类转录本。早期转录本在四个不同的基因组区域被鉴定出来。一个长度为4.8 kb的显著早期mRNA覆盖了位于复制起点和cos位点之间的一组12个基因。两个短的早期mRNA分别代表来自cos位点紧邻区域的一个基因和来自溶原模块的超感染免疫基因。第四个早期转录本覆盖了位于溶菌酶基因和整合酶基因之间的一组四个基因。长度为2.1 kb和5.8 kb的中期转录本分别覆盖了cro样和ant样阻遏基因以及DNA复制模块。鉴定出四种类型的晚期转录本。这些转录本分别覆盖了可能的DNA包装基因、头部形态发生模块加主要尾部基因、其余的尾部基因以及假定的尾丝加裂解基因。只有来自头部形态发生基因的转录本产生了明确的晚期mRNA种类。转录图谱与噬菌体Sfi21基因组组织的大多数计算机预测结果一致,除了DNA复制模块与可能的转录调控模块的分离。在引物延伸实验中确定的大多数转录本的5'端之前没有一致的启动子序列。氯霉素抑制实验表明噬菌体编码的调节因子参与中期和晚期转录。