Novel Gene Important For Craniofacial Development Implicated In Facial Cleft Birth Defects
Mice lacking the gene for Prdm16 exhibit numerous defects including a complete cleft of the secondary palate and a shortened mandible. In a study led by Dr. Dennis Warner and his co-investigators at the University of Louisville Birth Defects Center chromatin immunoprecipitation followed by array analysis was utilized to identify genes regulated by Prdm16 in cells isolated from the secondary palate of mouse embryos.
This approach revealed the developmental processes regulated by this protein that are important for palate development.
"Identifying the cellular and molecular processes regulated by PRDM16 is an important step toward elucidating the underlying mechanisms important for normal embryonic development of the head and face", said Dr. Warner.
Over 100 genes, whose promoters were bound by PRDM16 were identified. These genes were found to be linked to such diverse processes as chromatin remodeling and muscle and bone development.
Dr. Michele Pisano, a co-investigator on this study added that: "little is known of the factors governing differentiation of embryonic palate mesenchymal cells into bone or muscle. Our study suggests that Prdm16 may be critical for these processes." Demonstration that loss of Prdm16 expression led to a significant decrease in the expression of osteopontin, a marker for bone formation, and an increase in the expression of Myf-4, a marker for muscle development, support Dr. Pisano's contention.
Dr. Steven R. Goodman, Editor-in-Chief of Experimental Biology and Medicine, said "This important study by Warner and colleagues demonstrates that the transcription co-factor Prdm16 plays an important role in the normal development of the embryonic palate. They further demonstrate genes essential to muscle and bone development which are regulated by Prdm16 in cells isolated from the secondary palate of mouse embryos. This study should be of great significance in our understanding of birth defects leading to facial clefts."
Source: EurekAlert!, the online, global news service operated by AAAS, the science society
Please use one of the following formats to cite this article in your essay, paper or report:
Society for Experimental Biology and Medicine. "Novel Gene Important For Craniofacial Development Implicated In Facial Cleft Birth Defects." Medical News Today. MediLexicon, Intl., 4 May. 2012. Web.
30 May. 2016. <http://www.medicalnewstoday.com/releases/244943.php>
Society for Experimental Biology and Medicine. (2012, May 4). "Novel Gene Important For Craniofacial Development Implicated In Facial Cleft Birth Defects." Medical News Today. Retrieved from
Please note: If no author information is provided, the source is cited instead.
Contact our news editors
For any corrections of factual information, or to contact our editorial team, please see our contact page.
Copyright Medical News Today: Excluding email/sharing services explicitly offered on this website, material published on Medical News Today may not be reproduced, or distributed without the prior written permission of Medilexicon International Ltd. Please contact us for further details.