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Calcium signals act through histone deacetylase to mediate pronephric kidney morphogenesis
Author(s) -
Rothschild Sarah C.,
Lee Hunter J.,
Ingram Sarah R.,
Mohammadi Daniel K.,
Walsh Gregory S.,
Tombes Robert M.
Publication year - 2018
Publication title -
developmental dynamics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.634
H-Index - 141
eISSN - 1097-0177
pISSN - 1058-8388
DOI - 10.1002/dvdy.24632
Subject(s) - biology , cilium , polycystic kidney disease , microbiology and biotechnology , camk , morpholino , hdac4 , zebrafish , kidney , histone deacetylase , endocrinology , histone , genetics , protein kinase a , kinase , autophosphorylation , gene
Background: Autosomal dominant polycystic kidney disease is the most common monogenetic kidney disorder and is linked to mutations in PKD1 and PKD2. PKD2, a Ca 2+ ‐conducting TRP channel enriched in ciliated cells and gated by extracellular signals, is necessary to activate the multifunctional Ca 2+/ calmodulin–dependent protein kinase type 2 (CaMK‐II), enabling kidney morphogenesis and cilia stability. Results: In this study, antisense morpholino oligonucleotides and pharmacological compounds were employed to investigate the roles of class II HDAC family members (HDAC 4, 5, and 6) in Zebrafish kidney development. While all three class II HDAC genes were expressed throughout the embryo during early development, HDAC5‐morphant embryos exhibited anterior cysts and destabilized cloacal cilia, similar to PKD2 and CaMK‐II morphants. In contrast, HDAC4‐morphant embryos exhibited elongated cloacal cilia and lacked anterior kidney defects. Suppression of HDAC4 partially reversed the cilia shortening and anterior convolution defects caused by CaMK‐II deficiency, whereas HDAC5 loss exacerbated these defects. EGFP‐HDAC4, but not EGFP‐HDAC5, translocated into the nucleus upon CaMK‐II suppression in pronephric kidney cells. Conclusions: These results support a model by which activated CaMK‐II sequesters HDAC4 in the cytosol to enable primary cilia formation and kidney morphogenesis. Developmental Dynamics 247:807–817, 2018 . © 2018 Wiley Periodicals, Inc.