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cables1 is required for embryonic neural development: molecular, cellular, and behavioral evidence from the zebrafish
Author(s) -
Groeneweg Jolijn W.,
White Yvonne A.R.,
Kokel David,
Peterson Randall T.,
Zukerberg Lawrence R.,
Berin Inna,
Rueda Bo R.,
Wood Antony W.
Publication year - 2011
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.21263
Subject(s) - biology , zebrafish , gene knockdown , microbiology and biotechnology , morpholino , embryonic stem cell , neural development , ectopic expression , phenotype , neurogenesis , morphogenesis , genetics , apoptosis , gene
In vitro studies have suggested that the Cables1 gene regulates epithelial cell proliferation, whereas other studies suggest a role in promoting neural differentiation. In efforts to clarify the functions of Cables1 in vivo, we conducted gain‐ and loss‐of‐function studies targeting its ortholog ( cables1 ) in the zebrafish embryo. Similar to rodents, zebrafish cables1 mRNA expression is detected most robustly in embryonic neural tissues. Antisense knockdown of cables1 leads to increased numbers of apoptotic cells, particularly in brain tissue, in addition to a distinct behavioral phenotype, characterized by hyperactivity in response to stimulation. Apoptosis and the behavioral abnormality could be rescued by co‐expression of a morpholino‐resistant cables1 construct. Suppression of p53 expression in cables1 morphants partially rescued both apoptosis and the behavioral phenotype, suggesting that the phenotype of cables1 morphants is due in part to p53‐dependent apoptosis. Alterations in the expression patterns of several neural transcription factors were observed in cables1 morphants during early neurulation, suggesting that cables1 is required for early neural differentiation. Ectopic overexpression of cables1 strongly disrupted embryonic morphogenesis, while overexpression of a cables1 mutant lacking the C‐terminal cyclin box had little effect, suggesting functional importance of the cyclin box. Lastly, marked reductions in p35, but not Cdk5, were observed in cables1 morphants. Collectively, these data suggest that cables1 is important for neural differentiation during embryogenesis, in a mechanism that likely involves interactions with the Cdk5/p35 kinase pathway. Mol. Reprod. Dev. 78:22–32, 2011. © 2010 Wiley‐Liss, Inc.