Article ID Journal Published Year Pages File Type
2077765 Cell Stem Cell 2012 11 Pages PDF
Abstract

SummaryIn mouse skeletal muscles, Pax7 uniquely marks muscle satellite cells and plays some important yet unknown functions at the perinatal stage. To elucidate its in vivo functions, we initiated a yeast two-hybrid screening to look for Pax7-interacting proteins and identified a previously uncharacterized Pax7- and Pax3-binding protein (Pax3/7BP). Pax3/7BP is a ubiquitously expressed nuclear protein, enriched in Pax7+ muscle precursor cells (MPCs), and serves as an indispensable adaptor for Pax7 to recruit the histone 3 lysine 4 (H3K4) methyltransferase (HMT) complex by bridging Pax7 and Wdr5. Knockdown of Pax3/7BP abolished the Pax3/7-associated H3K4 HMT activity and inhibited the proliferation of Pax7+ MPCs from young mice both in culture and in vivo. Id3 and Cdc20 were direct target genes of Pax7 and Pax3/7BP involved in the proliferation of Pax7+ MPCs. Collectively, our work establishes Pax3/7BP as an essential adaptor linking Pax3/7 with the H3K4 HMT to regulate the proliferation of MPCs.

Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (193 K)Download as PowerPoint slideHighlights► Pax3/7BP physically interacts with both Pax7 and Pax3 in muscle precursor cells ► Pax3/7BP facilitates Pax7 to recruit H3K4 HMT by bridging Pax7 and Wdr5 ► Id3 and Cdc20 are direct target genes of Pax7 and Pax3/7BP ► Pax7 and Pax3/7BP regulate the proliferation of muscle precursor cells

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