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Plasticity of the Leishmania genome leading to gene copy number variations and drug resistance
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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
F1000Research
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031125/ https://www.ncbi.nlm.nih.gov/pubmed/27703673 http://dx.doi.org/10.12688/f1000research.9218.1 |
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author | Laffitte, Marie-Claude N. Leprohon, Philippe Papadopoulou, Barbara Ouellette, Marc |
author_facet | Laffitte, Marie-Claude N. Leprohon, Philippe Papadopoulou, Barbara Ouellette, Marc |
author_sort | Laffitte, Marie-Claude N. |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5031125 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | F1000Research |
record_format | MEDLINE/PubMed |
spelling | pubmed-50311252016-10-03 Plasticity of the Leishmania genome leading to gene copy number variations and drug resistance Laffitte, Marie-Claude N. Leprohon, Philippe Papadopoulou, Barbara Ouellette, Marc F1000Res Review 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. F1000Research 2016-09-20 /pmc/articles/PMC5031125/ /pubmed/27703673 http://dx.doi.org/10.12688/f1000research.9218.1 Text en Copyright: © 2016 Laffitte MCN et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Laffitte, Marie-Claude N. Leprohon, Philippe Papadopoulou, Barbara Ouellette, Marc Plasticity of the Leishmania genome leading to gene copy number variations and drug resistance |
title | Plasticity of the
Leishmania genome leading to gene copy number variations and drug resistance |
title_full | Plasticity of the
Leishmania genome leading to gene copy number variations and drug resistance |
title_fullStr | Plasticity of the
Leishmania genome leading to gene copy number variations and drug resistance |
title_full_unstemmed | Plasticity of the
Leishmania genome leading to gene copy number variations and drug resistance |
title_short | Plasticity of the
Leishmania genome leading to gene copy number variations and drug resistance |
title_sort | plasticity of the
leishmania genome leading to gene copy number variations and drug resistance |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031125/ https://www.ncbi.nlm.nih.gov/pubmed/27703673 http://dx.doi.org/10.12688/f1000research.9218.1 |
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