Modulation of gene expression in drug resistant Leishmania is associated with gene amplification, gene deletion and chromosome aneuploidy
-
* Corresponding author: Marc Ouellette Marc.Ouellette@crchul.ulaval.ca
1 Université Laval, Division de Microbiologie, Centre de Recherche en Infectiologie, boulevard Laurier, Québec, G1V 4G2, Canada
2 Université Laval, Centre de Recherche en Endocrinologie Moléculaire et Oncologique, boulevard Laurier, Québec, G1V 4G2, Canada
3 McGill University, Department of Microbiology and Immunology, Lyman Duff Medical Building, University Street, Montreal, H3A 2B4, Canada
Genome Biology 2008, 9:R115 doi:10.1186/gb-2008-9-7-r115
Published: 18 July 2008Additional files
Additional data file 1:
Differential expression measured by the full-genome microarray analysis.
Format: DOC Size: 5.4MB Download file
This file can be viewed with: Microsoft Word Viewer
Additional data file 2:
Figure S1 shows the direct repeats flanking the DHFR-TS locus of L. major and L. infantum chromosome 6, and also provides the circular junction sequence formed by homologous recombination. Figure S2 shows the inverted repeats present on chromosome 23 of L. infantum, and provides the sequence of the new junction formed through the inverted duplication. Figure S3 shows the sequence of the L. major chimera gene LmjF10.0380/0390.
Format: DOC Size: 89KB Download file
This file can be viewed with: Microsoft Word Viewer
Additional data file 3:
Results of the comparative genomic hybridization analyses of L. major MTX60.4 versus the respective wild-type cells.
Format: PPT Size: 196KB Download file
This file can be viewed with: Microsoft PowerPoint Viewer
