Generation of Sex-Reversed Female Clonal Mice via CRISPR-Cas9-Mediated Y Chromosome Deletion in Male Embryonic Stem Cells.
Animals
CRISPR-Cas Systems
Cell Line
Chromosome Deletion
Chromosomes, Human, Y
Clustered Regularly Interspaced Short Palindromic Repeats
Embryo, Mammalian
Embryonic Stem Cells
Female
Genotyping Techniques
Infertility, Male
Karyotyping
Male
Mice
Sex Chromosome Aberrations
Sex Chromosome Disorders of Sex Development
Y Chromosome
Journal
The CRISPR journal
ISSN: 2573-1602
Titre abrégé: CRISPR J
Pays: United States
ID NLM: 101738191
Informations de publication
Date de publication:
02 2021
02 2021
Historique:
pubmed:
11
2
2021
medline:
25
11
2021
entrez:
10
2
2021
Statut:
ppublish
Résumé
Mice derived entirely from embryonic stem (ES) cells can be generated through tetraploid complementation. Although XY male ES cell lines are commonly used in this system, occasionally, monosomic XO female mice are produced through spontaneous Y chromosome loss. Here, we describe an efficient method to obtain monosomic XO ES cells by CRISPR-Cas9-mediated deletion of the Y chromosome, allowing generation of female clonal mice by tetraploid complementation. The monosomic XO female mice are viable and able to produce normal male and female offspring. Direct generation of clonal mice in both sexes can significantly accelerate the production of complex genetically modified mouse models.
Identifiants
pubmed: 33567216
doi: 10.1089/crispr.2020.0074
pmc: PMC7898403
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
147-154Subventions
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Organisme : NIGMS NIH HHS
ID : R01 GM129380
Pays : United States
Organisme : NCI NIH HHS
ID : R35 CA210100
Pays : United States
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