Is TALPID3 a PCP Pathway Protein?

Louise Stephen, Lynn McTeir, Katie McTeir, John James, Megan Davey

Research output: Contribution to conferenceAbstract

Abstract / Description of output

The TALPID3 gene is essential for normal development in chickens, mice and zebrafish. Embryos without normal TALPID3 function lack cilia and have associated developmental abnormalities such as polydactyly, a loss of ventral neurons and polycystic kidneys. Hedgehog signalling is defective in TALPID3-/- embryos due to an accumulation of cytoplasmic full length Gli proteins. TALPID3 is known to localise to the cytoskeleton and to the centrosome, an organelle essential for ciliogenesis. The cilia and centrosome are required for both Hedgehog and Wnt/PCP signalling. TALPID3 has traditionally been studied as a Hedgehog pathway mutant, but many of its phenotypes may also be classed as traits of a PCP pathway mutant.
Original languageEnglish
Publication statusPublished - 18 Mar 2013
EventBritish Society for Developmental Biology - Warwick, United Kingdom
Duration: 17 Mar 201320 Mar 2013

Conference

ConferenceBritish Society for Developmental Biology
Country/TerritoryUnited Kingdom
CityWarwick
Period17/03/1320/03/13

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