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Chromodomain Helicase DNA Binding Protein 1 (Chd1) is required for orofacial development in Xenopus

Abnormalities affecting orofacial development are some of the most common, expensive, and devastating birth defects. Children born with such defects may experience difficulties with eating, breathing, and speech and in addition, these defects often require multiple surgeries to correct them. Therefore, it is critical to understand how the orofacial region develops in order to better treat and prevent these types of birth defects. Xenopus laevis has emerged as a strong model in which to examine orofacial development and was utilized here to investigate the cellular and molecular mechanisms underlying the complex development of the orofacial region. Retinoic acid is one signal involved in orchestrating orofacial development and accomplishes this in part by regulating the nucleosome structure of target genes. The work presented here characterizes the role of an ATP-dependent chromatin remodeler, chromodomain helicase DNA binding protein 1 (Chd1), in orofacial development in X. laevis. The spatial expression of Chd1 supports its role in orofacial development and reduced expression of Chd1 resulted in abnormal facial development. Closer examination of Chd1 morphant embryos revealed that Chd1 is required for the expression of important neural crest and cartilage genes that are necessary for proper development of the face. In addition, there was an increase in apoptosis in regions consistent with migrating neural crest and neural crest derived structures. As a consequence, many of the facial cartilages do not form properly in morphant embryos resulting in a smaller face. Further, this work presents evidence that Chd1 may cooperate with retinoic acid to regulate orofacial development in X. laevis.

Identiferoai:union.ndltd.org:vcu.edu/oai:scholarscompass.vcu.edu:etd-6434
Date01 January 2018
CreatorsWyatt, Brent
PublisherVCU Scholars Compass
Source SetsVirginia Commonwealth University
Detected LanguageEnglish
Typetext
Formatapplication/pdf
SourceTheses and Dissertations
Rights© Brent Wyatt

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