Open AccessThe MAPK Erk5 is necessary for proper skeletogenesis through a molecular axis that involves Smurfs-Smads-Sox9
Author(s) -
Takashi Iezaki,
Kazuya Fukasawa,
Tetsuhiro Horie,
Gyujin Park,
Samuel T. Robinson,
Michio Nakaya,
Hiroyuki Fujita,
Yuki Onishi,
Kakeru Ozaki,
Takashi Kanayama,
Manami Hiraiwa,
Yuka Kitaguchi,
Katsuyuki Kaneda,
Yukio Yoneda,
Takeshi Takarada,
Xing Guo,
Hitoshi Kurose,
Eiichi Hinoi
Publication year - 2018
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.164004
Subject(s) - smad , biology , microbiology and biotechnology , sox9 , ubiquitin ligase , mesenchymal stem cell , phosphorylation , transcription factor , mapk/erk pathway , smad2 protein , kinase , signal transduction , protein kinase a , ubiquitin , genetics , gene
Extracellular signal-regulated kinase 5 (Erk5) belongs to the mitogen-activated protein kinase (MAPK) family. Following its phosphorylation by MAPK/Erk kinase-5 (Mek5), Erk5 modulates several signaling pathways in a number of cell types. In this study, we demonstrated that Erk5 inactivation in mesenchymal cells causes abnormalities in skeletal development by inducing Sox9, an important transcription factor of skeletogenesis. We further demonstrated that Erk5 directly phosphorylates and activates Smurf2 (a ubiquitin E3 ligase) at Thr249, which promotes the proteasomal degradation of Smad proteins and phosphorylates Smad1 at Ser206 in the linker region known to trigger its proteasomal degradation by Smurf1. Smads transcriptionally activated the expression of Sox9 in mesenchymal cells. Accordingly, removal of one Sox9 allele in mesenchymal cells from Erk5-deficient mice rescued some abnormalities of skeletogenesis. These findings highlight the importance of the Mek5-Erk5-Smurfs-Smads-Sox9 axis in mammalian skeletogenesis.