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MBE Advance Access originally published online on November 24, 2004
Molecular Biology and Evolution 2005 22(3):639-649; doi:10.1093/molbev/msi057
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Molecular Biology and Evolution vol. 22 no. 3 © Society for Molecular Biology and Evolution 2004; all rights reserved.

Research Article

Survey of Simple Sequence Repeats in Completed Fungal Genomes

Haydar Karaoglu*,{dagger}, Crystal Man Ying Lee{dagger} and Wieland Meyer{dagger},{ddagger}

* School of Molecular and Microbial Biosciences, University of Sydney, Sydney, Australia; {dagger} Molecular Mycology Research Laboratory, CIDM, Westmead Hospital, Westmead, Australia; and {ddagger} Department of Medicine, Western Clinical School, University of Sydney, Sydney, Australia

E-mail: w.meyer{at}usyd.edu.au.

The use of simple sequence repeats or microsatellites as genetic markers has become very popular because of their abundance and length variation between different individuals. SSRs are tandem repeat units of 1 to 6 base pairs that are found abundantly in many prokaryotic and eukaryotic genomes. This is the first study examining and comparing SSRs in completely sequenced fungal genomes. We analyzed and compared the occurrences, relative abundance, relative density, most common, and longest SSRs in nine taxonomically different fungal species: Aspergillus nidulans, Cryptococcus neoformans, Encephalitozoon cuniculi, Fusarium graminearum, Magnaporthe grisea, Neurospora crassa, Saccharomyces cerevisiae, Schizosaccharomyces pombe, and Ustilago maydis. Our analysis revealed that, in all of the genomes studied, the occurrence, abundance, and relative density of SSRs varied and was not influenced by the genome sizes. No correlation between relative abundance and the genome sizes was observed, but it was shown that N. crassa, the largest genome analyzed had the highest relative abundance of SSRs. In most genomes, mononucleotide, dinucleotide, and trinucleotide repeats were more abundant than the longer repeated SSRs. Generally, in each organism, the occurrence, relative abundance, and relative density of SSRs decreased as the repeat unit increased. Furthermore, each organism had its own common and longest SSRs. Our analysis showed that the relative abundance of SSRs in fungi is low compared with the human genome and that longer SSRs in fungi are rare. In addition to providing new information concerning the abundance of SSRs for each of these fungi, the results provide a general source of molecular markers that could be useful for a variety of applications such as population genetics and strain identification of fungal organisms.

Key Words: simple sequence repeat • microsatellite • fungi


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