Cargando…

Genome Editing Using Mammalian Haploid Cells

Haploid cells are useful for studying gene functions because disruption of a single allele can cause loss-of-function phenotypes. Recent success in generating haploid embryonic stem cells (ESCs) in mice, rats, and monkeys provides a new platform for simple genetic manipulation of the mammalian genom...

Descripción completa

Detalles Bibliográficos
Autores principales: Horii, Takuro, Hatada, Izuho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632716/
https://www.ncbi.nlm.nih.gov/pubmed/26437403
http://dx.doi.org/10.3390/ijms161023604
_version_ 1782399079725137920
author Horii, Takuro
Hatada, Izuho
author_facet Horii, Takuro
Hatada, Izuho
author_sort Horii, Takuro
collection PubMed
description Haploid cells are useful for studying gene functions because disruption of a single allele can cause loss-of-function phenotypes. Recent success in generating haploid embryonic stem cells (ESCs) in mice, rats, and monkeys provides a new platform for simple genetic manipulation of the mammalian genome. Use of haploid ESCs enhances the genome-editing potential of the CRISPR/Cas system. For example, CRISPR/Cas was used in haploid ESCs to generate multiple knockouts and large deletions at high efficiency. In addition, genome-wide screening is facilitated by haploid cell lines containing gene knockout libraries.
format Online
Article
Text
id pubmed-4632716
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-46327162015-11-23 Genome Editing Using Mammalian Haploid Cells Horii, Takuro Hatada, Izuho Int J Mol Sci Review Haploid cells are useful for studying gene functions because disruption of a single allele can cause loss-of-function phenotypes. Recent success in generating haploid embryonic stem cells (ESCs) in mice, rats, and monkeys provides a new platform for simple genetic manipulation of the mammalian genome. Use of haploid ESCs enhances the genome-editing potential of the CRISPR/Cas system. For example, CRISPR/Cas was used in haploid ESCs to generate multiple knockouts and large deletions at high efficiency. In addition, genome-wide screening is facilitated by haploid cell lines containing gene knockout libraries. MDPI 2015-10-01 /pmc/articles/PMC4632716/ /pubmed/26437403 http://dx.doi.org/10.3390/ijms161023604 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Horii, Takuro
Hatada, Izuho
Genome Editing Using Mammalian Haploid Cells
title Genome Editing Using Mammalian Haploid Cells
title_full Genome Editing Using Mammalian Haploid Cells
title_fullStr Genome Editing Using Mammalian Haploid Cells
title_full_unstemmed Genome Editing Using Mammalian Haploid Cells
title_short Genome Editing Using Mammalian Haploid Cells
title_sort genome editing using mammalian haploid cells
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632716/
https://www.ncbi.nlm.nih.gov/pubmed/26437403
http://dx.doi.org/10.3390/ijms161023604
work_keys_str_mv AT horiitakuro genomeeditingusingmammalianhaploidcells
AT hatadaizuho genomeeditingusingmammalianhaploidcells