Notch directly regulates the cell morphogenesis genes Reck, talin and trio in adult muscle progenitors

• Published in: Journal of cell science Vol. 127; no. Pt 21; pp. 4634 - 4644
• Main Authors: Pézeron, Guillaume, Millen, Kat, Boukhatmi, Hadi, Bray, Sarah
• Format: Journal Article
• Language: English
• Published: England Company of Biologists 01-11-2014; The Company of Biologists
• Subjects: Animals; Cellular Biology; Development Biology; Drosophila; Drosophila Proteins - genetics; Drosophila Proteins - metabolism; Guanine Nucleotide Exchange Factors - genetics; Guanine Nucleotide Exchange Factors - metabolism; In Situ Hybridization; Life Sciences; Muscle Development - genetics; Muscle Development - physiology; Muscles - cytology; Muscles - metabolism; Phosphoproteins - genetics; Phosphoproteins - metabolism; Protein Serine-Threonine Kinases - genetics; Protein Serine-Threonine Kinases - metabolism; Receptors, Notch - genetics; Receptors, Notch - metabolism; Reverse Transcriptase Polymerase Chain Reaction; Stem Cells - cytology; Stem Cells - metabolism; Subcellular Processes; Talin - genetics; Talin - metabolism; Trio; Drosophila; Gene regulation; Notch; Talin; Reck; Myogenesis
• ISSN: 0021-9533; 1477-9137
• DOI: 10.1242/jcs.151787

There is growing evidence that activation of the Notch pathway can result in consequences on cell morphogenesis and behaviour, both during embryonic development and cancer progression. In general, Notch is proposed to coordinate these processes by regulating expression of key transcription factors. However, many Notch-regulated genes identified in genome-wide studies are involved in fundamental aspects of cell behaviour, suggesting a more direct influence on cellular properties. By testing the functions of 25 such genes we confirmed that 12 are required in developing adult muscles, consistent with roles downstream of Notch. Focusing on three, Reck, rhea/talin and trio, we verify their expression in adult muscle progenitors and identify Notch-regulated enhancers in each. Full activity of these enhancers requires functional binding sites for Su(H), the DNA-binding transcription factor in the Notch pathway, validating their direct regulation. Thus, besides its well-known roles in regulating the expression of cell-fate-determining transcription factors, Notch signalling also has the potential to directly affect cell morphology and behaviour by modulating expression of genes such as Reck, rhea/talin and trio. This sheds new light on the functional outputs of Notch activation in morphogenetic processes.