Vahanian Nicole, Oh Choon Seok, Sippy Jean, Feiss Michael
Department of Microbiology, Roy J. and Lucille A. Carver College of Medicine University of Iowa, Iowa City, IA 52242, USA.
Department of Microbiology, Roy J. and Lucille A. Carver College of Medicine University of Iowa, Iowa City, IA 52242, USA.
Virology. 2017 Sep;509:140-145. doi: 10.1016/j.virol.2017.06.016. Epub 2017 Jun 21.
The base pairs of cosN, the site where the 12 base-long cohesive ends are generated in λ-like phages, show partial-two fold rotational symmetry. In a bioinformatic survey, we found that the cosN changes in 12 natural cosN variants are restricted to bp 6-to-12 of the cohesive end sequence. In contrast, bp 1-5 of the cohesive end sequence are strictly conserved (13/13), as are the two bp flanking the left nicking site (bp -2 and -1). The bp flanking the right nick site (bp 13 and 14) are conserved in 12 of 13 variants. Five cosN variants differing by as many as five bp were used to replace lambda's cosN. No significant effects of the cosN changes on λ's virus yield were found. In sum, bp -2 to 5 are critical cosN function, and bp 6-12 of the cohesive end sequence are not critical for terminase recognition or virus fitness.
在类λ噬菌体中产生12个碱基长的粘性末端的位点cosN,其碱基对呈现部分二重旋转对称性。在一项生物信息学调查中,我们发现12个天然cosN变体中的cosN变化仅限于粘性末端序列的第6至12个碱基对。相比之下,粘性末端序列的第1至5个碱基对严格保守(13/13),左切口位点两侧的两个碱基对(第 -2和 -1个碱基对)也是如此。右切口位点两侧的碱基对(第13和14个碱基对)在13个变体中的12个中保守。使用了多达5个碱基对不同的5个cosN变体来取代λ的cosN。未发现cosN变化对λ病毒产量有显著影响。总之,第 -2至5个碱基对是cosN功能的关键,粘性末端序列的第6至12个碱基对对于末端酶识别或病毒适应性并不关键。