Pedersen Margit, Kilstrup Mogens, Hammer Karin
Department of Microbial Physiology and Genetics, BioCentrum-DTU, Technical University of Denmark, DK-2800 Lyngby, Denmark.
Virology. 2006 Feb 20;345(2):446-56. doi: 10.1016/j.virol.2005.10.007. Epub 2005 Nov 17.
Alt, encoded by the lactococcal phage TP901-1, is needed for late transcription. We identify Alt as a DNA-binding protein, and footprint analysis shows that Alt binds to a region containing four imperfect direct repeats (ALT boxes) located -76 to -32 relative to the P(late) transcriptional start site. The importance of the ALT boxes was confirmed by deletion of one or two ALT boxes and by introducing mutations in ALT boxes 1 and 4. Alt is proposed to act as a tetramer or higher multimer activating transcription of TP901-1 late genes by binding to the four ALT boxes, and bending of the DNA may be important for transcriptional activation of P(late). Furthermore, our results suggest that DNA replication may be required for late transcription in TP901-1. Additionally, we identify gp28 of the related lactococcal phage Tuc2009 as an activator and show that the activators required for late transcription in TP901-1 and Tuc2009 are interchangeable.
由乳球菌噬菌体TP901-1编码的Alt是晚期转录所必需的。我们鉴定出Alt是一种DNA结合蛋白,足迹分析表明Alt结合到一个区域,该区域包含四个不完全直接重复序列(ALT框),相对于P(晚期)转录起始位点位于-76至-32处。通过缺失一个或两个ALT框以及在ALT框1和4中引入突变,证实了ALT框的重要性。有人提出Alt作为四聚体或更高阶多聚体,通过结合四个ALT框来激活TP901-1晚期基因的转录,并且DNA的弯曲对于P(晚期)的转录激活可能很重要。此外,我们的结果表明DNA复制可能是TP901-1晚期转录所必需的。另外,我们鉴定出相关乳球菌噬菌体Tuc2009的gp28作为激活剂,并表明TP901-1和Tuc2009晚期转录所需的激活剂是可互换的。