4.0 Article

Widely Expressed Af17 is Likely not Required for Embryogenesis, Hematopoiesis, and Animal Survival

Journal

GENESIS
Volume 48, Issue 12, Pages 693-706

Publisher

WILEY
DOI: 10.1002/dvg.20679

Keywords

AF17; MLL6; gene trap; X-gal staining; RT-PCR; leukemia; isthmus; olfactory pit; dorsal root ganglia; central nervous system; brain; kidney; heart; testis; spleen; lung; liver; uterus; eye; bladder; salivary gland; stomach

Funding

  1. American Heart Association [0865271F]
  2. National Institutes of Health [R01 DK080236]
  3. American Society of Nephrology
  4. NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES [R01DK080236] Funding Source: NIH RePORTER

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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. genesis 48:693-706, 2010. (C) 2010 Wiley-Liss, Inc.

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