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Rapidly generating knockout mice from H19-Igf2 engineered androgenetic haploid embryonic stem cells.


ABSTRACT: Haploid mammalian embryonic stem cells (ESCs) hold great promise for functional genetic studies and assisted reproduction. Recently, rodent androgenetic haploid ESCs (AG-haESCs) were generated from androgenetic blastocysts and functioned like sperm to produce viable offspring via the intracytoplasmic AG-haESCs injection into oocytes. However, the efficiency of this reproduction was very low. Most pups were growth-retarded and died shortly after birth, which is not practical for producing knockout animals. Further investigation suggested a possible link between the low birthrate and aberrant expression of imprinted genes. Here, we report the high-frequency generation of healthy, fertile mice from H19-Igf2 imprinting-locus modified AG-haESCs, which maintained normal paternal imprinting and pluripotency. Moreover, it is feasible to perform further genetic manipulations in these AG-haESCs. Our study provides a reliable and efficient tool to rapidly produce gene-modified mouse models and will benefit reproductive medicine in the future.

SUBMITTER: Zhang M 

PROVIDER: S-EPMC4860787 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Rapidly generating knockout mice from H19-Igf2 engineered androgenetic haploid embryonic stem cells.

Zhang Meili M   Liu Yufang Y   Liu Guang G   Li Xin X   Jia Yuyan Y   Sun Lihong L   Wang Liu L   Zhou Qi Q   Huang Yue Y  

Cell discovery 20151103


Haploid mammalian embryonic stem cells (ESCs) hold great promise for functional genetic studies and assisted reproduction. Recently, rodent androgenetic haploid ESCs (AG-haESCs) were generated from androgenetic blastocysts and functioned like sperm to produce viable offspring via the intracytoplasmic AG-haESCs injection into oocytes. However, the efficiency of this reproduction was very low. Most pups were growth-retarded and died shortly after birth, which is not practical for producing knockou  ...[more]

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