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Plasticity of the Leishmania genome leading to gene copy number variations and drug resistance [version 1; referees: 5 approved]
- Source :
- F1000Research. 5:F1000 Faculty Rev-2350
- Publication Year :
- 2016
- Publisher :
- London, UK: F1000 Research Limited, 2016.
-
Abstract
- Leishmania has a plastic genome, and drug pressure can select for gene copy number variation (CNV). CNVs can apply either to whole chromosomes, leading to aneuploidy, or to specific genomic regions. For the latter, the amplification of chromosomal regions occurs at the level of homologous direct or inverted repeated sequences leading to extrachromosomal circular or linear amplified DNAs. This ability of Leishmania to respond to drug pressure by CNVs has led to the development of genomic screens such as Cos-Seq, which has the potential of expediting the discovery of drug targets for novel promising drug candidates.
- Subjects :
- Review
Articles
Bioinformatics
Cell Growth & Division
Cell Signaling
Cellular Death & Stress Responses
Evolutionary/Comparative Genetics
Genomics
Medical Microbiology
Microbial Evolution & Genomics
Nuclear Structure & Function
Parasitology
Leishmania
Ploidy
Drug Resistance
Mode of action
Cos-Seq
Subjects
Details
- ISSN :
- 20461402
- Volume :
- 5
- Database :
- F1000Research
- Journal :
- F1000Research
- Notes :
- Editorial Note on the Review Process F1000 Faculty Reviews are commissioned from members of the prestigious F1000 Faculty and are edited as a service to readers. In order to make these reviews as comprehensive and accessible as possible, the referees provide input before publication and only the final, revised version is published. The referees who approved the final version are listed with their names and affiliations but without their reports on earlier versions (any comments will already have been addressed in the published version). The referees who approved this article are: Gerald Spaeth, Unité de Parasitologie moléculaire et Signalisation, Department of Parasites and Insect Vectors, Institut Pasteur, INSERM U1201, Paris, France No competing interests were disclosed. Yvon Sterkers, UMR MIVEGEC (CNRS 5290 - IRD 224 - University Montpellier), University Regional Hospital of Montpellier, Montpellier, France No competing interests were disclosed. Richard McCulloch, The Wellcome Trust Centre for Molecular Parasitology, Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK No competing interests were disclosed. Joachim Clos, Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany No competing interests were disclosed. Francisco Gamarro, Instituto de Parasitología Lopez-Neyra, IPBLN-CSIC, Granada, Spain No competing interests were disclosed., , [version 1; referees: 5 approved]
- Publication Type :
- Academic Journal
- Accession number :
- edsfor.10.12688.f1000research.9218.1
- Document Type :
- review
- Full Text :
- https://doi.org/10.12688/f1000research.9218.1