A multiple site-specific DNA-inversion model for the control of Ompi phase and antigenic variation in Dichelobacter nodosus

1995 ◽  
Vol 17 (1) ◽  
pp. 183-196 ◽  
Author(s):  
Eric K. Moses ◽  
Robert T. Good ◽  
Meri Sinistaj ◽  
Stephen J. Billington ◽  
Christopher J. Langford ◽  
...  
Microbiology ◽  
2005 ◽  
Vol 151 (3) ◽  
pp. 935-940 ◽  
Author(s):  
Joanne L. Allen ◽  
Amir H. Noormohammadi ◽  
Glenn F. Browning

Mycoplasma synoviae, a major pathogen of poultry, contains a single expressed, full-length vlhA gene encoding its haemagglutinin, and a large number of vlhA pseudogenes that can be recruited by multiple site-specific recombination events to generate chimaeric variants of the expressed gene. The position and distribution of the vlhA pseudogene regions, and their relationship with the expressed gene, have not been investigated. To determine the relationship between these regions, a physical map of the M. synoviae genome was constructed using the restriction endonucleases SmaI, I-CeuI, BsiWI, ApaI and XhoI and radiolabelled probes for rrnA, recA and tufA. A cloned fragment encoding the unique portion of the expressed vlhA gene and two PCR products containing conserved regions of the ORF 3 and ORF 6 vlhA pseudogenes were used to locate the regions containing these genes on the map. The chromosome of M. synoviae was found to be 890·4 kb and the two rRNA operons were in the same orientation. Both the expressed vlhA gene and the vlhA pseudogenes were confined to the same 114 kb region of the chromosome. These findings indicate that, unlike Mycoplasma gallisepticum, in which the vlhA genes are located in several loci around the chromosome and in which antigenic variation is generated by alternating transcription of over 40 translationally competent genes, M. synoviae has all of the vlhA sequences clustered together, suggesting that close proximity is needed to facilitate the site-specific recombinations used to generate diversity in the expressed vlhA gene.


1993 ◽  
Vol 175 (3) ◽  
pp. 693-700 ◽  
Author(s):  
L Dorgai ◽  
J Oberto ◽  
R A Weisberg
Keyword(s):  

2000 ◽  
Vol 182 (10) ◽  
pp. 2787-2792 ◽  
Author(s):  
Atsuko Gyohda ◽  
Teruya Komano

ABSTRACT The shufflon, a multiple DNA inversion system in plasmid R64, consists of four invertible DNA segments which are separated and flanked by seven 19-bp repeat sequences. The product of a site-specific recombinase gene, rci, promotes site-specific recombination between any two of the inverted 19-bp repeat sequences of the shufflon. To analyze the molecular mechanism of this recombination reaction, Rci protein was overproduced and purified. The purified Rci protein promoted the in vitro recombination reaction between the inverted 19-bp repeats of supercoiled DNA of a plasmid carrying segment A of the R64 shufflon. The recombination reaction was enhanced by the bacterial host factor HU. Gel electrophoretic analysis indicated that the Rci protein specifically binds to the DNA segments carrying the 19-bp sequences. The binding affinity of the Rci protein to the four shufflon segments as well as four synthetic 19-bp sequences differed greatly: among the four 19-bp repeat sequences, the repeat-a and -d sequences displayed higher affinity to Rci protein. These results suggest that the differences in the affinity of Rci protein for the 19-bp repeat sequences determine the inversion frequencies of the four segments.


1985 ◽  
Vol 82 (11) ◽  
pp. 3776-3780 ◽  
Author(s):  
H. E. Huber ◽  
S. Iida ◽  
W. Arber ◽  
T. A. Bickle

BioEssays ◽  
1987 ◽  
Vol 7 (5) ◽  
pp. 195-200 ◽  
Author(s):  
Roland Kanaar ◽  
Pieter van de Putte
Keyword(s):  

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