The aim of this application is to study the function of the newly discovered mouse gene Foxi3 during development of the craniofacial sensory organs. All craniofacial sensory organs derive from a pan-placodal domain which surrounds the neural plate. Much of the pan-placodal domain is believed to be competent to give rise to each craniofacial sensory organ and is specified by receiving signals from neighboring tissues such as the neural plate, mesoderm and endoderm. Since the beginning of the 20th century, a number of craniofacial birth defects have been identified. Many of these present as multiple defects in craniofacial organs. In addition, recent studies have shown that zebrafish foxi1 is required for otic and jaw development. Thus, we hypothesize that mouse Foxi3 plays crucial roles during craniofacial development. Here, we propose to test this hypothesis in the following specific aims: 1) To determine the lineage of the descendants of Foxi3-expressing cells during cranial placode development. We will generate Foxi3-Cre BAG transgenic mice and mate them with Cre-loxP reporter mice. 2) To assess the loss-of-function of Foxi3 in placodal cell fate specification. We will generate Foxi3 knockout mice. 3) To assess the necessity of the down-regulation of Foxi3 in otic placode specification. We will generate floxed """"""""stop""""""""+Foxi3 transgenic mice and mate them with the Pax2-Cre mice. This project has significant potential for the future study of craniofacial and sensory organ development that will shed light on the genetic mechanisms of craniofacial birth defects. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Small Research Grants (R03)
Project #
1R03DC007349-01A1
Application #
7033601
Study Section
Special Emphasis Panel (ZDC1-SRB-Y (54))
Program Officer
Freeman, Nancy
Project Start
2006-01-12
Project End
2008-11-30
Budget Start
2006-01-12
Budget End
2006-11-30
Support Year
1
Fiscal Year
2006
Total Cost
$93,250
Indirect Cost
Name
House Research Institute
Department
Type
DUNS #
062076989
City
Los Angeles
State
CA
Country
United States
Zip Code
90057
Birol, Onur; Ohyama, Takahiro; Edlund, Renée K et al. (2016) The mouse Foxi3 transcription factor is necessary for the development of posterior placodes. Dev Biol 409:139-151
Shirokova, Vera; Biggs, Leah C; Jussila, Maria et al. (2016) Foxi3 Deficiency Compromises Hair Follicle Stem Cell Specification and Activation. Stem Cells 34:1896-908
Jussila, Maria; Aalto, Anne J; Sanz Navarro, Maria et al. (2015) Suppression of epithelial differentiation by Foxi3 is essential for molar crown patterning. Development 142:3954-63
Edlund, Renée K; Ohyama, Takahiro; Kantarci, Husniye et al. (2014) Foxi transcription factors promote pharyngeal arch development by regulating formation of FGF signaling centers. Dev Biol 390:1-13