Rpn (YhgA-Like) Proteins of Escherichia coli K-12 and Their Contribution to RecA-Independent Horizontal Transfer

被引:20
作者
Kingston, Anthony W. [1 ]
Ponkratz, Christine [1 ]
Raleigh, Elisabeth A. [1 ]
机构
[1] New England Biolabs Inc, Ipswich, MA 01938 USA
关键词
DNA damage; conjugation; evolutionary biology; gene function; genomic instability; horizontal gene transfer; illegitimate recombination; protein function; protein motif; transposase; PD-(D/E)XK NUCLEASES; GENE-TRANSFER; FREE CA2+; ENDONUCLEASE; RESTRICTION; IDENTIFICATION; RECOMBINATION; SEQUENCE; PURIFICATION; RECOGNITION;
D O I
10.1128/JB.00787-16
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Bacteria use a variety of DNA-mobilizing enzymes to facilitate environmental niche adaptation via horizontal gene transfer. This has led to real-world problems, like the spread of antibiotic resistance, yet many mobilization proteins remain undefined. In the study described here, we investigated the uncharacterized family of YhgA-like transposase_31 (Pfam PF04754) proteins. Our primary focus was the genetic and biochemical properties of the five Escherichia coli K-12 members of this family, which we designate RpnA to RpnE, where Rpn represents recombination-promoting nuclease. We employed a conjugal system developed by our lab that demanded RecA-independent recombination following transfer of chromosomal DNA. Overexpression of RpnA (YhgA), RpnB (YfcI), RpnC (YadD), and RpnD (YjiP) increased RecA-independent recombination, reduced cell viability, and induced the expression of reporter of DNA damage. For the exemplar of the family, RpnA, mutational changes in proposed catalytic residues reduced or abolished all three phenotypes in concert. In vitro, RpnA displayed magnesium-dependent, calcium-stimulated DNA endonuclease activity with little, if any, sequence specificity and a preference for double-strand cleavage. We propose that Rpn/YhgA-like family nucleases can participate in gene acquisition processes.
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页数:17
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