| Literature DB >> 29945867 |
Theresa Schredelseker1,2, Wolfgang Driever3,2.
Abstract
Neuroendocrine cells in the pineal gland release melatonin during the night and, in teleosts, are directly photoreceptive. During development of the pineal complex, a small number of cells migrate leftward away from the pineal anlage to form the parapineal cell cluster, a process that is crucial for asymmetrical development of the bilateral habenular nuclei. Here, we show that, throughout zebrafish embryonic development, the brain-specific homeobox (bsx) gene is expressed in all cell types of the pineal complex. We identified Bmp and Noto/Flh as major regulators of bsx expression in the pineal complex. Upon loss of Bsx through the generation of a targeted mutation, embryos fail to form a parapineal organ and develop right-isomerized habenulae. Crucial enzymes in the melatonin biosynthesis pathway are not expressed, suggesting the absence of melatonin from the pineal gland in bsx mutants. Several genes involved in rod-like or cone-like phototransduction are also abnormally expressed, indicating that Bsx has a pivotal role in the differentiation of multiple cell types in the zebrafish pineal complex.Entities:
Keywords: Brain asymmetry; Brain-specific homeobox transcription factor; Bsx; Epithalamus; Habenula; Melatonin; Parapineal organ; Photoreceptors; Pineal gland
Mesh:
Substances:
Year: 2018 PMID: 29945867 DOI: 10.1242/dev.163477
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868