Sequence determinants for DNA packaging specificity in the S-aureus pathogenicity island SaPI1

被引:15
作者
Bento, Joana C. [1 ,3 ]
Lane, Kristin D. [1 ]
Read, Erik K. [2 ]
Cerca, Nuno [3 ]
Christie, Gail E. [1 ]
机构
[1] Virginia Commonwealth Univ, Sch Med, Dept Microbiol & Immunol, Richmond, VA 23298 USA
[2] Food & Drug Adm, Ctr Drug Evaluat & Res, Div Monoclonal Antibodies, Silver Spring, MD 20993 USA
[3] Univ Minho, Ctr Biol Engn, IBB, P-4710057 Braga, Portugal
关键词
Pathogenicity island; SaPI; Terminase; DNA packaging; Helper phage; Pac site; CAPSID SIZE DETERMINATION; GRAM-POSITIVE BACTERIA; HELPER PHAGE; PROTEINS; SITE; BACTERIOPHAGES; INTERFERENCE; REPLICATION; RECOGNITION; INITIATION;
D O I
10.1016/j.plasmid.2013.12.001
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The SaPIs and their relatives are a family of genomic islands that exploit helper phages for high frequency horizontal transfer. One of the mechanisms used by SaPIs to accomplish this molecular piracy is the redirection of the helper phage DNA packaging machinery. SaPls encode a small terminase subunit that can be substituted for that of the phage. In this study we have determined the initial packaging cleavage sites for helper phage 80a, which uses the phage-encoded small terminase subunit, and for SaPI1, which uses the SaPI-encoded small terminase subunit. We have identified a 19 nt SaPI1 sequence that is necessary and sufficient to allow high frequency 80a transduction of a plasmid by a terminase carrying the SaPI1-encoded small subunit. We also show that the hybrid enzyme with the SaPI1 small terminase subunit is capable of generalized transduction. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:8 / 15
页数:8
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