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Open Access Research article

A novel substitution matrix fitted to the compositional bias in Mollicutes improves the prediction of homologous relationships

Claire Lemaitre12*, Aurélien Barré1, Christine Citti34, Florence Tardy5, François Thiaucourt6, Pascal Sirand-Pugnet78 and Patricia Thébault19

Author Affiliations

1 Université de Bordeaux, Centre de Bioinformatique et Génomique Fonctionnelle Bordeaux, F-33000 Bordeaux, France

2 Equipe SYMBIOSE, INRIA Rennes Bretagne Atlantique, Campus de Beaulieu, F-35042 Rennes, France

3 Université de Toulouse, ENVT, UMR 1225, F-31076 Toulouse, France

4 INRA, UMR 1225, F-31076 Toulouse, France

5 Anses, Lyon Laboratory, UMR Mycoplasmoses of Ruminants, 31 Avenue Tony Garnier F-69364 Lyon cedex 07, France

6 CIRAD, UMR CMAEE, Campus de Baillarguet, F-34398 Montpellier, France

7 Université de Bordeaux, UMR 1332, 71, avenue Edouard Bourlaux, F-33140 Villenave d'Ornon, France

8 INRA, UMR 1332, 71, avenue Edouard Bourlaux, F-33140 Villenave d'Ornon, France

9 Université de Bordeaux, Laboratoire Bordelais de Recherche en Informatique, UMR 5800, F-33405 Talence, France

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BMC Bioinformatics 2011, 12:457  doi:10.1186/1471-2105-12-457

Published: 24 November 2011

Abstract

Background

Substitution matrices are key parameters for the alignment of two protein sequences, and consequently for most comparative genomics studies. The composition of biological sequences can vary importantly between species and groups of species, and classical matrices such as those in the BLOSUM series fail to accurately estimate alignment scores and statistical significance with sequences sharing marked compositional biases.

Results

We present a general and simple methodology to build matrices that are especially fitted to the compositional bias of proteins. Our approach is inspired from the one used to build the BLOSUM matrices and is based on learning substitution and amino acid frequencies on real sequences with the corresponding compositional bias. We applied it to the large scale comparison of Mollicute AT-rich genomes. The new matrix, MOLLI60, was used to predict pairwise orthology relationships, as well as homolog families among 24 Mollicute genomes. We show that this new matrix enables to better discriminate between true and false orthologs and improves the clustering of homologous proteins, with respect to the use of the classical matrix BLOSUM62.

Conclusions

We show in this paper that well-fitted matrices can improve the predictions of orthologous and homologous relationships among proteins with a similar compositional bias. With the ever-increasing number of sequenced genomes, our approach could prove valuable in numerous comparative studies focusing on atypical genomes.