Evolutionary Dynamics of the mS952 Intron: A Novel Mitochondrial Group II Intron Encoding a LAGLIDADG Homing Endonuclease Gene

2011 ◽  
Vol 72 (5-6) ◽  
pp. 433-449 ◽  
Author(s):  
Sahra-Taylor Mullineux ◽  
Karla Willows ◽  
Georg Hausner
PLoS ONE ◽  
2013 ◽  
Vol 8 (1) ◽  
pp. e54130 ◽  
Author(s):  
Yuk-Sang Chan ◽  
David S. Huen ◽  
Ruth Glauert ◽  
Eleanor Whiteway ◽  
Steven Russell

RNA ◽  
2010 ◽  
Vol 16 (9) ◽  
pp. 1818-1831 ◽  
Author(s):  
S.-T. Mullineux ◽  
M. Costa ◽  
G. S. Bassi ◽  
F. Michel ◽  
G. Hausner

PLoS ONE ◽  
2012 ◽  
Vol 7 (11) ◽  
pp. e49551 ◽  
Author(s):  
Anja Pfeifer ◽  
Bettina Martin ◽  
Jörg Kämper ◽  
Christoph W. Basse

2005 ◽  
Vol 33 (3) ◽  
pp. 482-484 ◽  
Author(s):  
Å.B. Birgisdottir ◽  
S.D. Johansen

A mobile group I intron containing two ribozyme domains and a homing endonuclease gene (twin-ribozyme intron organization) can integrate by reverse splicing into the small subunit rRNA of bacteria and yeast. The integration is sequence-specific and corresponds to the natural insertion site (homing site) of the intron. The reverse splicing is independent of the homing endonuclease gene, but is dependent on the group I splicing ribozyme domain. The observed distribution of group I introns in nature can be explained by horizontal transfer between natural homing sites by reverse splicing and subsequent spread in populations by endonuclease-dependent homing.


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