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Norway

PMID:21170927  

Widely expressed Af17 is likely not required for embryogenesis, hematopoiesis, and animal survival.

Zhijing Zhang | Le Huang | Mary Rose Reisenauer | Hongyu Wu | Lihe Chen | Yujin Zhang | Yang Xia | Wenzheng Zhang
Genesis (New York, N.Y. : 2000) | 2010

As a putative transcription factor, Af17 may play a role in multiple signaling pathways. However, the Af17 expression profile during development and in adult tissues remains largely uncharacterized. The importance of Af17 function in embryogenesis, hematopoiesis, and animal survival has never been addressed before. Here we report the generation of the first Af17 mutant mouse model and characterization of the Af17 temporal and spatial expression profile in various embryonic stages and adult tissues by X-gal staining, in situ hybridization, and RT-PCR. Af17 expression is detected in specific cell populations in all stages and in multiple tissues examined. In situ hybridization yielded a consistent Af17 expression pattern by X-gal staining. Homozygous mutant mice are viable, fertile, normal in size, and do not display any gross physical, behavioral, or hematopoietic abnormalities. Thus, our studies describe the generation of the first Af17 mutant mouse model, provide the first developmental profile of Af17 expression, and reveal that Af17 may be dispensable for normal embryogenesis, hematopoiesis, and animal survival.

Pubmed ID: 21170927

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Associated grants

  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK080236
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK080236-01A1
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK080236-02
  • Agency: NIDDK NIH HHS, United States
    Id: R01 DK080236-03

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SIGTR ES cell line AC0433 (organism)

RRID:MMRRC_020107-UCD

Mus musculus with name SIGTR ES cell line AC0433 from MMRRC.

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