» Articles » PMID: 20511499

Neisseria Gonorrhoeae FA1090 Carries Genes Encoding Two Classes of Vsr Endonucleases

Overview
Journal J Bacteriol
Specialty Microbiology
Date 2010 Jun 1
PMID 20511499
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

A very short patch repair system prevents mutations resulting from deamination of 5-methylcytosine to thymine. The Vsr endonuclease is the key enzyme of this system, providing sequence specificity. We identified two genes encoding Vsr endonucleases V.NgoAXIII and V.NgoAXIV from Neisseria gonorrhoeae FA1090 based on DNA sequence similarity to genes encoding Vsr endonucleases from other bacteria. After expression of the gonococcal genes in Escherichia coli, the proteins were biochemically characterized and the endonucleolytic activities and specificities of V.NgoAXIII and V.NgoAXIV were determined. V.NgoAXIII was found to be multispecific and to recognize T:G mismatches in every nucleotide context tested, whereas V.NgoAXIV recognized T:G mismatches in the following sequences: GTGG, CTGG, GTGC, ATGC, and CTGC. Alanine mutagenesis of conserved residues showed that Asp50 and His68 of V.NgoAXIII and Asp51 and His69 of V.NgoAXIV are essential for hydrolytic activity. Glu25, His64, and Asp97 of V.NgoAXIV and Glu24, Asp63, and Asp97 of V.NgoAXIII are important but not crucial for the activity of V.NgoAXIII and V.NgoAXIV. However, Glu24 and Asp63 are also important for the specificity of V.NgoAXIII. On the basis of our results concerning features of Vsr endonucleases expressed by N. gonorrhoeae FA1090, we postulate that at least two types of Vsr endonucleases can be distinguished.

Citing Articles

Genetic variation regulates the activation and specificity of Restriction-Modification systems in Neisseria gonorrhoeae.

Sanchez-Buso L, Golparian D, Parkhill J, Unemo M, Harris S Sci Rep. 2019; 9(1):14685.

PMID: 31605008 PMC: 6789123. DOI: 10.1038/s41598-019-51102-2.


Activity of Vsr endonucleases encoded by Neisseria gonorrhoeae FA1090 is influenced by MutL and MutS proteins.

Adamczyk-Poplawska M, Bandyra K, Kwiatek A BMC Microbiol. 2018; 18(1):95.

PMID: 30165819 PMC: 6116569. DOI: 10.1186/s12866-018-1243-3.


DNA Methylation Assessed by SMRT Sequencing Is Linked to Mutations in Neisseria meningitidis Isolates.

Sater M, Lamelas A, Wang G, Clark T, Roltgen K, Mane S PLoS One. 2015; 10(12):e0144612.

PMID: 26656597 PMC: 4676702. DOI: 10.1371/journal.pone.0144612.


The dam replacing gene product enhances Neisseria gonorrhoeae FA1090 viability and biofilm formation.

Kwiatek A, Bacal P, Wasiluk A, Trybunko A, Adamczyk-Poplawska M Front Microbiol. 2015; 5:712.

PMID: 25566225 PMC: 4269198. DOI: 10.3389/fmicb.2014.00712.


Diverse functions of restriction-modification systems in addition to cellular defense.

Vasu K, Nagaraja V Microbiol Mol Biol Rev. 2013; 77(1):53-72.

PMID: 23471617 PMC: 3591985. DOI: 10.1128/MMBR.00044-12.

References
1.
Kwiatek A, Kobes M, Olejnik K, Piekarowicz A . DNA methyltransferases from Neisseria meningitidis and Neisseria gonorrhoeae FA1090 associated with mismatch nicking endonucleases. Microbiology (Reading). 2004; 150(Pt 6):1713-1722. DOI: 10.1099/mic.0.27011-0. View

2.
Tsutakawa S, Muto T, Kawate T, Jingami H, Kunishima N, Ariyoshi M . Crystallographic and functional studies of very short patch repair endonuclease. Mol Cell. 1999; 3(5):621-8. DOI: 10.1016/s1097-2765(00)80355-x. View

3.
Lieb M, Rehmat S . Very short patch repair of T:G mismatches in vivo: importance of context and accessory proteins. J Bacteriol. 1995; 177(3):660-6. PMC: 176641. DOI: 10.1128/jb.177.3.660-666.1995. View

4.
Tsutakawa S, Jingami H, Morikawa K . Recognition of a TG mismatch: the crystal structure of very short patch repair endonuclease in complex with a DNA duplex. Cell. 1999; 99(6):615-23. DOI: 10.1016/s0092-8674(00)81550-0. View

5.
Gunn J, Stein D . Natural variation of the NgoII restriction-modification system of Neisseria gonorrhoeae. Gene. 1993; 132(1):15-20. DOI: 10.1016/0378-1119(93)90509-2. View