Blatny J M, Ventura M, Rosenhaven E M, Risøen P A, Lunde M, Brüssow H, Nes I F
Laboratory of Microbial Gene Technology, Department of Chemistry and Biotechnology, Agricultural University of Norway, P.O. Box 5051, 1432 As, Norway.
Mol Genet Genomics. 2003 Jul;269(4):487-98. doi: 10.1007/s00438-003-0854-y. Epub 2003 May 21.
A transcriptional analysis of the lysogeny-related genes of the temperate bacteriophage Lactococcus lactis phiLC3 was performed using Northern blot hybridization during lysogeny and lytic infection by the phage. The lysogeny-related gene cluster was found to contain four promoters (P(1), P(2), Pint and P(173)), while the P(87) promoter directed transcription of orf80 and the putative gene orf87, which are located between the integrase gene and the cell lysis genes. The start sites of the transcripts were determined by primer extension. The divergently oriented lysogenic P(1) and lytic P(2) promoters located in the genetic switch region are responsible for transcription of orf286 which encodes the phage repressor, and the genes orf63 - orf76 - orf236 - orf110 - orf82 - orf57, respectively, while orf173 is transcribed from P(173). orf76 was identified as the gene encoding the Cro-like protein of phiLC3, and it was shown that ORF76 is able to bind specifically to the genetic switch region, albeit with lower affinity than does the phage repressor ORF286. ORF76 also competed with ORF286 for binding to this region. The functionality of P(1) and P(2), and their regulation by ORF286 and ORF76, was investigated using a reporter gene. In general, P(2) was a stronger promoter than P(1), but expression from both promoters, especially P(2), was regulated and modulated by flanking sequences and the presence of orf286 and orf76. ORF286 and ORF76 were both able to repress transcription from P(1) and P(2), while ORF286 was able to stimulate its own synthesis by tenfold. This work reveals the complex interplay between the regulatory elements that control the genetic switch between lysis and lysogeny in phiLC3 and other temperate phages of Lactococcus.
在温和噬菌体乳酸乳球菌phiLC3的溶原化和裂解感染过程中,利用Northern印迹杂交技术对其与溶原化相关的基因进行了转录分析。发现与溶原化相关的基因簇包含四个启动子(P(1)、P(2)、Pint和P(173)),而P(87)启动子指导位于整合酶基因和细胞裂解基因之间的orf80和推定基因orf87的转录。通过引物延伸确定了转录本的起始位点。位于遗传开关区域的方向相反的溶原性P(1)和裂解性P(2)启动子分别负责编码噬菌体阻遏物的orf286以及基因orf63 - orf76 - orf236 - orf110 - orf82 - orf57的转录,而orf173由P(173)转录。orf76被鉴定为编码phiLC3的Cro样蛋白的基因,并且表明ORF76能够特异性结合遗传开关区域,尽管其亲和力低于噬菌体阻遏物ORF286。ORF76也与ORF286竞争结合该区域。使用报告基因研究了P(1)和P(2)的功能及其受ORF286和ORF76的调控。一般来说,P(2)是比P(1)更强的启动子,但两个启动子的表达,尤其是P(2)的表达,受到侧翼序列以及orf286和orf76的存在的调控和调节。ORF286和ORF76都能够抑制P(1)和P(2)的转录,而ORF286能够将其自身的合成刺激10倍。这项工作揭示了控制phiLC3和乳酸乳球菌其他温和噬菌体中裂解和溶原化之间遗传开关的调控元件之间的复杂相互作用。