PUBLICATION

Zebrafish Paralogs brd2a and brd2b Are Needed for Proper Circulatory, Excretory and Central Nervous System Formation and Act as Genetic Antagonists during Development

Authors
Branigan, G.L., Olsen, K.S., Burda, I., Haemmerle, M.W., Ho, J., Venuto, A., D'Antonio, N.D., Briggs, I.E., DiBenedetto, A.J.
ID
ZDB-PUB-211130-11
Date
2021
Source
Journal of developmental biology   9(4): (Journal)
Registered Authors
DiBenedetto, Angela
Keywords
BET proteins, bromodomain, cell death, functional antagonism, gene duplication, gene interaction, lineage specification, peripheral blood island, pronephros, spinal interneuron
MeSH Terms
none
PubMed
34842711 Full text @ J Dev Biol
Abstract
Brd2 belongs to the BET family of epigenetic transcriptional co-regulators that act as adaptor-scaffolds for the assembly of chromatin-modifying complexes and other factors at target gene promoters. Brd2 is a protooncogene and candidate gene for juvenile myoclonic epilepsy in humans, a homeobox gene regulator in Drosophila, and a maternal-zygotic factor and cell death modulator that is necessary for normal development of the vertebrate central nervous system (CNS). As two copies of Brd2 exist in zebrafish, we use antisense morpholino knockdown to probe the role of paralog Brd2b, as a comparative study to Brd2a, the ortholog of human Brd2. A deficiency in either paralog results in excess cell death and dysmorphology of the CNS, whereas only Brd2b deficiency leads to loss of circulation and occlusion of the pronephric duct. Co-knockdown of both paralogs suppresses single morphant defects, while co-injection of morpholinos with paralogous RNA enhances them, suggesting novel genetic interaction with functional antagonism. Brd2 diversification includes paralog-specific RNA variants, a distinct localization of maternal factors, and shared and unique spatiotemporal expression, providing unique insight into the evolution and potential functions of this gene.
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