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CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites
The development of the CRISPR-Cas system is revolutionizing genome editing in a variety of organisms. The system has now been used to manipulate the genome of Plasmodium falciparum, the most lethal malaria-causing species. The ability to generate gene deletions or nucleotide substitutions rapidly an...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254425/ https://www.ncbi.nlm.nih.gov/pubmed/25473431 http://dx.doi.org/10.1186/s13073-014-0063-9 |
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author | Lee, Marcus CS Fidock, David A |
author_facet | Lee, Marcus CS Fidock, David A |
author_sort | Lee, Marcus CS |
collection | PubMed |
description | The development of the CRISPR-Cas system is revolutionizing genome editing in a variety of organisms. The system has now been used to manipulate the genome of Plasmodium falciparum, the most lethal malaria-causing species. The ability to generate gene deletions or nucleotide substitutions rapidly and economically promises to accelerate the analysis of novel drug targets and to help elucidate the function of specific genes or gene families, while complementing genome-wide association studies. |
format | Online Article Text |
id | pubmed-4254425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42544252014-12-04 CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites Lee, Marcus CS Fidock, David A Genome Med Research Highlight The development of the CRISPR-Cas system is revolutionizing genome editing in a variety of organisms. The system has now been used to manipulate the genome of Plasmodium falciparum, the most lethal malaria-causing species. The ability to generate gene deletions or nucleotide substitutions rapidly and economically promises to accelerate the analysis of novel drug targets and to help elucidate the function of specific genes or gene families, while complementing genome-wide association studies. BioMed Central 2014-08-26 /pmc/articles/PMC4254425/ /pubmed/25473431 http://dx.doi.org/10.1186/s13073-014-0063-9 Text en © Lee and Fidock; licensee BioMed Central Ltd. 2014 The licensee has exclusive rights to distribute this article, in any medium, for 12 months following its publication. After this time, the article is available under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Highlight Lee, Marcus CS Fidock, David A CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites |
title | CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites |
title_full | CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites |
title_fullStr | CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites |
title_full_unstemmed | CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites |
title_short | CRISPR-mediated genome editing of Plasmodium falciparum malaria parasites |
title_sort | crispr-mediated genome editing of plasmodium falciparum malaria parasites |
topic | Research Highlight |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4254425/ https://www.ncbi.nlm.nih.gov/pubmed/25473431 http://dx.doi.org/10.1186/s13073-014-0063-9 |
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