کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2077765 | 1079742 | 2012 | 11 صفحه PDF | دانلود رایگان |

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 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
Journal: - Volume 11, Issue 2, 3 August 2012, Pages 231–241