Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow Print PDF (284K) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (7)
Right arrowRequest Permissions
Right arrow Commercial Re-use Guidelines
for Open Access NAR Content
Google Scholar
Right arrow Articles by Leh-Louis, V.
Right arrow Articles by Souciet, J. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Leh-Louis, V.
Right arrow Articles by Souciet, J. L.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published online 15 April 2004

Nucleic Acids Research, 2004, Vol. 32, No. 7 2069-2078
© 2004 Oxford University Press

Differential evolution of the Saccharomyces cerevisiae DUP240 paralogs and implication of recombination in phylogeny

V. Leh-Louis, B. Wirth, L. Despons, S. Wain-Hobson1, S. Potier and J. L. Souciet*

Laboratoire de Microbiologie et Génétique, FRE 2326 Université Louis Pasteur/CNRS, Institut de Botanique, F-67083 Strasbourg Cedex, France and 1 Unité de Rétrovirologie Moléculaire, Institut Pasteur, F-75724 Paris Cedex 15, France

*To whom correspondence should be addressed. Tel: +33 3 90 24 18 17; Fax: +33 3 90 24 20 28; Email: souciet{at}gem.u-strasbg.fr
The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors

Received November 18, 2003; Revised February 5, 2004; Accepted March 16, 2004

Multigene families are observed in all genomes sequenced so far and are the reflection of key evolutionary mechanisms. The DUP240 family, identified in Saccharomyces cerevisiae strain S288C, is composed of 10 paralogs: seven are organized as two tandem repeats and three are solo ORFs. To investigate the evolution of the three solo paralogs, YAR023c, YCR007c and YHL044w, we performed a comparative analysis between 15 S.cerevisiae strains. These three ORFs are present in all strains and the conservation of synteny indicates that they are not frequently involved in chromosomal reshaping, in contrast to the DUP240 ORFs organized in tandem repeats. Our analysis of nucleotide and amino acid variations indicates that YAR023c and YHL044w fix mutations more easily than YCR007c, although they all belong to the same multigene family. This comparative analysis was also conducted with five arbitrarily chosen Ascomycetes-specific genes and five arbitrarily chosen common genes (genes that have a homolog in at least one non-Ascomycetes organism). Ascomycetes-specific genes appear to be diverging faster than common genes in the S.cerevisiae species, a situation that was previously described between different yeast species. Our results point to the strong contribution, during DNA sequence evolution, of allelic recombination besides nucleotide substitution.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Biol EvolHome page
B. Wirth, V. L. Louis, S. Potier, J.-L. Souciet, and L. Despons
Paleogenomics or the Search for Remnant Duplicated Copies of the Yeast DUP240 Gene Family in Intergenic Areas
Mol. Biol. Evol., September 1, 2005; 22(9): 1764 - 1771.
[Abstract] [Full Text] [PDF]


Home page
GeneticsHome page
V. Leh-Louis, B. Wirth, S. Potier, J.-L. Souciet, and L. Despons
Expansion and Contraction of the DUP240 Multigene Family in Saccharomyces cerevisiae Populations
Genetics, August 1, 2004; 167(4): 1611 - 1619.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.