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The mitochondrial transporter SLC25A25 links ciliary TRPP2 signaling and cellular metabolism

Cilia are organelles specialized in movement and signal transduction. The ciliary transient receptor potential ion channel polycystin-2 (TRPP2) controls elementary cilia-mediated physiological functions ranging from male fertility and kidney development to left–right patterning. However, the molecul...

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Detalles Bibliográficos
Autores principales: Hofherr, Alexis, Seger, Claudia, Fitzpatrick, Fiona, Busch, Tilman, Michel, Elisabeth, Luan, Jingting, Osterried, Lea, Linden, Frieder, Kramer-Zucker, Albrecht, Wakimoto, Barbara, Schütze, Conny, Wiedemann, Nils, Artati, Anna, Adamski, Jerzy, Walz, Gerd, Kunji, Edmund R. S., Montell, Craig, Watnick, Terry, Köttgen, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6095617/
https://www.ncbi.nlm.nih.gov/pubmed/30080851
http://dx.doi.org/10.1371/journal.pbio.2005651
Descripción
Sumario:Cilia are organelles specialized in movement and signal transduction. The ciliary transient receptor potential ion channel polycystin-2 (TRPP2) controls elementary cilia-mediated physiological functions ranging from male fertility and kidney development to left–right patterning. However, the molecular components translating TRPP2 channel–mediated Ca(2+) signals into respective physiological functions are unknown. Here, we show that the Ca(2+)-regulated mitochondrial ATP-Mg/P(i) solute carrier 25 A 25 (SLC25A25) acts downstream of TRPP2 in an evolutionarily conserved metabolic signaling pathway. We identify SLC25A25 as an essential component in this cilia-dependent pathway using a genome-wide forward genetic screen in Drosophila melanogaster, followed by a targeted analysis of SLC25A25 function in zebrafish left–right patterning. Our data suggest that TRPP2 ion channels regulate mitochondrial SLC25A25 transporters via Ca(2+) establishing an evolutionarily conserved molecular link between ciliary signaling and mitochondrial metabolism.