Wnt signaling from the dorsal neural tube is required for the formation of the medial dermomyotome

• DOI: 10.1242/dev.125.24.4969
• Publication Date: 2021-04-26T03:28:46Z
• Authors: Makoto Ikeya; Shinji Takada
• Keywords: Mice, Knockout; 0301 basic medicine; Gene Expression Regulation, Developmental; Muscle Proteins; Proteins; Cell Differentiation; Muscle Development; DNA-Binding Proteins; Repressor Proteins; Embryonic and Fetal Development; Mice; 03 medical and health sciences; Somites; Proto-Oncogene Proteins; Basic Helix-Loop-Helix Transcription Factors; Animals; Paired Box Transcription Factors; Muscle, Skeletal; PAX3 Transcription Factor; In Situ Hybridization; Body Patterning; Signal Transduction

ABSTRACT Signals originating from tissues surrounding somites are involved in mediolateral and dorsoventral patterning of somites and in the differentiation of the myotome. Wnt-1 and Wnt-3a, which encode members of the Wnt family of cystein-rich secreted signaling molecules, are coexpressed at the dorsal midline of the developing neural tube, an area adjacent to the dorsomedial portion of the somite. Several lines of evidence indicate that Wnt-1 and Wnt-3a have the ability to induce the development of the medial and dorsal portion of somites, as well as to induce myogenesis. To address whether these Wnt signalings are really essential for the development of somites during normal embryogenesis, we investigated the development of somites in mouse embryos lacking both Wnt-1 and Wnt-3a. Here we demonstrate that the medial compartment of the dermomyotome is not formed and the expression of a lateral dermomyotome marker gene, Sim-1, is expanded more medially in the absence of these Wnt signalings. In addition, the expression of a myogenic gene, Myf-5, is decreased at 9.5 days post coitum whereas the level of expression of a number of myogenic genes in the later stage appeared normal. These results indicate that Wnt-1 and Wnt-3a signalings actually regulate the formation of the medial compartment of the dermomyotome and the early part of myogenesis.