| Literature DB >> 26947080 |
Clayton B Marshall1, Deborah J Mays1, J Scott Beeler1, Jennifer M Rosenbluth2, Kelli L Boyd3, Gabriela L Santos Guasch1, Timothy M Shaver1, Lucy J Tang1, Qi Liu4, Yu Shyr5, Bryan J Venters6, Mark A Magnuson6, Jennifer A Pietenpol7.
Abstract
We report that p73 is expressed in multiciliated cells (MCCs), is required for MCC differentiation, and directly regulates transcriptional modulators of multiciliogenesis. Loss of ciliary biogenesis provides a unifying mechanism for many phenotypes observed in p73 knockout mice including hydrocephalus; hippocampal dysgenesis; sterility; and chronic inflammation/infection of lung, middle ear, and sinus. Through p73 and p63 ChIP-seq using murine tracheal cells, we identified over 100 putative p73 target genes that regulate MCC differentiation and homeostasis. We validated Foxj1, a transcriptional regulator of multiciliogenesis, and many other cilia-associated genes as direct target genes of p73 and p63. We show p73 and p63 are co-expressed in a subset of basal cells and suggest that p73 marks these cells for MCC differentiation. In summary, p73 is essential for MCC differentiation, functions as a critical regulator of a transcriptome required for MCC differentiation, and, like p63, has an essential role in development of tissues.Entities:
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Year: 2016 PMID: 26947080 PMCID: PMC4794398 DOI: 10.1016/j.celrep.2016.02.035
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423