Posts Tagged ‘Protein interaction’

Identifying components of complexes

January 1, 2008

Goffard N, Weiller G.

Methods Mol Biol (2008) vol. 453 pp. 257-65

Identifying and analyzing components of complexes is essential to understand the activities and organization of the cell. Moreover, it provides additional information on the possible function of proteins involved in these complexes. Two bioinformatics approaches are usually used for this purpose. The first is based on the identification, by clustering algorithms, of full or densely connected sub-graphs in protein-protein interaction networks derived from experimental sources that might represent complexes. The second approach consists of the integration of genomic and proteomic data by using Bayesian networks or decision trees. This approach is based on the hypothesis that proteins involved in a complex usually share common properties.

Genome evolution in yeasts

July 1, 2004

Dujon B, Sherman D, Fischer G, Durrens P, Casaregola S, Lafontaine I, De Montigny J, Marck C, Neuvéglise C, Talla E, Goffard N, Frangeul L, Aigle M, Anthouard V, Babour A, Barbe V, Barnay S, Blanchin S, Beckerich JM, Beyne E, Bleykasten C, Boisramé A, Boyer J, Cattolico L, Confanioleri F, de Daruvar A, Despons L, Fabre E, Fairhead C, Ferry-Dumazet H, Groppi A, Hantraye F, Hennequin C, Jauniaux N, Joyet P, Kachouri R, Kerrest A, Koszul R, Lemaire M, Lesur I, Ma L, Muller H, Nicaud JM, Nikolski M, Oztas S, Ozier-Kalogeropoulos O, Pellenz S, Potier S, Richard GF, Straub ML, Suleau A, Swennen D, Tekaia F, Wésolowski-Louvel M, Westhof E, Wirth B, Zeniou-Meyer M, Zivanovic I, Bolotin-Fukuhara M, Thierry A, Bouchier C, Caudron B, Scarpelli C, Gaillardin C, Weissenbach J, Wincker P, Souciet JL.

Nature (2004) vol. 430 (6995) pp. 35-44

Identifying the mechanisms of eukaryotic genome evolution by comparative genomics is often complicated by the multiplicity of events that have taken place throughout the history of individual lineages, leaving only distorted and superimposed traces in the genome of each living organism. The hemiascomycete yeasts, with their compact genomes, similar lifestyle and distinct sexual and physiological properties, provide a unique opportunity to explore such mechanisms. We present here the complete, assembled genome sequences of four yeast species, selected to represent a broad evolutionary range within a single eukaryotic phylum, that after analysis proved to be molecularly as diverse as the entire phylum of chordates. A total of approximately 24,200 novel genes were identified, the translation products of which were classified together with Saccharomyces cerevisiae proteins into about 4,700 families, forming the basis for interspecific comparisons. Analysis of chromosome maps and genome redundancies reveal that the different yeast lineages have evolved through a marked interplay between several distinct molecular mechanisms, including tandem gene repeat formation, segmental duplication, a massive genome duplication and extensive gene loss.

IPPRED: server for proteins interactions inference

May 1, 2003

Goffard N, Garcia V, Iragne F, Groppi A, de Daruvar A.

Bioinformatics (2003) vol. 19 (7) pp. 903-4

IPPRED is a web based server to infer protein-protein interactions through homology search between candidate proteins and those described as interacting. This simple inference allows to propose or to validate potential interactions.
AVAILABILITY: IPPRED is freely available at http://cbi.labri.fr/outils/ippred/.


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