Unique spatiotemporal requirements for intraflagellar transport genes during forebrain development

• Published in: PloS one Vol. 12; no. 3; p. e0173258
• Main Authors: Snedeker, John, Schock, Elizabeth N, Struve, Jamie N, Chang, Ching-Fang, Cionni, Megan, Tran, Pamela V, Brugmann, Samantha A, Stottmann, Rolf W
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 14.03.2017; Public Library of Science (PLoS)
• Subjects: Ablation; Adaptor Proteins, Signal Transducing - genetics; Animals; Arthritis; Binding sites; Biological Transport - genetics; Biology and Life Sciences; Brain; Cell cycle; Cell development (Biology); Cilia; Cilia - physiology; Cortex; Defects; Developmental biology; Ectoderm; Embryos; Forebrain; Genes; Genetics; Hospitals; Kidney diseases; Kinesin - genetics; Medicine and Health Sciences; Mice; Mice, Knockout; Microtubules; Mutation; Neural crest; Organelles; Pediatrics; Physiological aspects; Prosencephalon - embryology; Proteins; Stem cells; Transport; Tumor Suppressor Proteins - genetics; United States
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0173258

Primary cilia are organelles extended from virtually all cells and are required for the proper regulation of a number of canonical developmental pathways. The role in cortical development of proteins important for ciliary form and function is a relatively understudied area. Here we have taken a genetic approach to define the role in forebrain development of three intraflagellar transport proteins known to be important for primary cilia function. We have genetically ablated Kif3a, Ift88, and Ttc21b in a series of specific spatiotemporal domains. The resulting phenotypes allow us to draw several conclusions. First, we conclude that the Ttc21b cortical phenotype is not due to the activity of Ttc21b within the brain itself. Secondly, some of the most striking phenotypes are from ablations in the neural crest cells and the adjacent surface ectoderm indicating that cilia transduce critical tissue-tissue interactions in the developing embryonic head. Finally, we note striking differences in phenotypes from ablations only one embryonic day apart, indicating very discrete spatiotemporal requirements for these three genes in cortical development.