CFAP157 is a murine downstream effector of FOXJ1 that is specifically required for flagellum morphogenesis and sperm motility.
Marina WeidemannKarin Schuster-GosslerMichael StauberChristoph WredeJan HegermannTim OttKarsten BoldtTina BeyerKatrin SerthElisabeth KremmerMartin BlumMarius UeffingAchim GosslerPublished in: Development (Cambridge, England) (2017)
Motile cilia move extracellular fluids or mediate cellular motility. Their function is essential for embryonic development, adult tissue homeostasis and reproduction throughout vertebrates. FOXJ1 is a key transcription factor for the formation of motile cilia but its downstream genetic programme is only partially understood. Here, we characterise a novel FOXJ1 target, Cfap157, that is specifically expressed in motile ciliated tissues in mouse and Xenopus in a FOXJ1-dependent manner. CFAP157 protein localises to basal bodies and interacts with tubulin and the centrosomal protein CEP350. Cfap157 knockout mice appear normal but homozygous males are infertile. Spermatozoa display impaired motility and a novel phenotype: Cfap157-deficient sperm exhibit axonemal loops, supernumerary axonemal profiles with ectopic accessory structures, excess cytoplasm and clustered mitochondria in the midpiece regions, and defective axonemes along the flagella. Our study thus demonstrates an essential sperm-specific function for CFAP157 and suggests that this novel FOXJ1 effector is part of a mechanism that acts during spermiogenesis to suppress the formation of supernumerary axonemes and ensures a correct ultrastructure.
Keyphrases
- biofilm formation
- transcription factor
- binding protein
- regulatory t cells
- dendritic cells
- gene expression
- high resolution
- protein protein
- randomized controlled trial
- cell death
- study protocol
- genome wide
- metabolic syndrome
- cystic fibrosis
- escherichia coli
- clinical trial
- skeletal muscle
- young adults
- reactive oxygen species
- dna binding
- copy number
- wild type