Amalgam plays a dual role in controlling the number of leg muscle progenitors and regulating their interactions with the developing Drosophila tendon

• Published in: PLoS biology Vol. 22; no. 10; p. e3002842
• Main Authors: Moucaud, Blandine, Prince, Elodie, Ragot, Elia, Renaud, Yoan, Jagla, Krzysztof, Junion, Guillaume, Soler, Cedric
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01.10.2024
• Subjects: Animals; Biology and Life Sciences; Cell Communication; Cell Differentiation; Cell Proliferation; Drosophila - metabolism; Drosophila melanogaster - genetics; Drosophila melanogaster - growth & development; Drosophila melanogaster - metabolism; Drosophila Proteins - genetics; Drosophila Proteins - metabolism; Extremities - embryology; Gene Expression Regulation, Developmental; Medicine and Health Sciences; Muscle Development - genetics; Muscle, Skeletal - growth & development; Muscle, Skeletal - metabolism; Myoblasts - metabolism; Research and Analysis Methods; Signal Transduction; Stem Cells - cytology; Stem Cells - metabolism; Tendons - cytology; Tendons - embryology; Tendons - metabolism
• ISSN: 1545-7885; 1544-9173; 1545-7885
• DOI: 10.1371/journal.pbio.3002842

Formation of functional organs requires cell-cell communication between different cell lineages and failure in this communication can result in severe developmental defects. Hundreds of possible interacting pairs of proteins are known, but identifying the interacting partners that ensure a specific interaction between 2 given cell types remains challenging. Here, we use the Drosophila leg model and our cell type-specific transcriptomic data sets to uncover the molecular mediators of cell-cell communication between tendon and muscle precursors. Through the analysis of gene expression signatures of appendicular muscle and tendon precursor cells, we identify 2 candidates for early interactions between these 2 cell populations: Amalgam (Ama) encoding a secreted protein and Neurotactin (Nrt) known to encode a membrane-bound protein. Developmental expression and function analyses reveal that: (i) Ama is expressed in the leg myoblasts, whereas Nrt is expressed in adjacent tendon precursors; and (ii) in Ama and Nrt mutants, myoblast-tendon cell-cell association is lost, leading to tendon developmental defects. Furthermore, we demonstrate that Ama acts downstream of the FGFR pathway to maintain the myoblast population by promoting cell survival and proliferation in an Nrt-independent manner. Together, our data pinpoint Ama and Nrt as molecular actors ensuring early reciprocal communication between leg muscle and tendon precursors, a prerequisite for the coordinated development of the appendicular musculoskeletal system.