Brain-specific homeobox Bsx specifies identity of pineal gland between serially homologous photoreceptive organs in zebrafish

The pineal gland functioning as a photoreceptive organ in non-mammalian species is a serial homolog of the retina. Here we found that Brain-specific homeobox (Bsx) is a key regulator conferring individuality on the pineal gland between the two serially homologous photoreceptive organs in zebrafish....

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Published inCommunications biology Vol. 2; no. 1; p. 364
Main Authors Mano, Hiroaki, Asaoka, Yoichi, Kojima, Daisuke, Fukada, Yoshitaka
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 07.10.2019
Nature Publishing Group
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ISSN2399-3642
2399-3642
DOI10.1038/s42003-019-0613-1

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Summary:The pineal gland functioning as a photoreceptive organ in non-mammalian species is a serial homolog of the retina. Here we found that Brain-specific homeobox (Bsx) is a key regulator conferring individuality on the pineal gland between the two serially homologous photoreceptive organs in zebrafish. Bsx knock-down impaired the pineal development with reduced expression of exorh , the pineal-specific gene responsible for the photoreception, whereas it induced ectopic expression of rho , a retina-specific gene, in the pineal gland. Bsx remarkably transactivated the exorh promoter in combination with Otx5, but not with Crx, through its binding to distinct subtypes of PIRE, a DNA cis -element driving Crx/Otx-dependent pineal-specific gene expression. These results demonstrate that the identity of pineal photoreceptive neurons is determined by the combinatorial code of Bsx and Otx5, the former confers the pineal specificity at the tissue level and the latter determines the photoreceptor specificity at the cellular level. Hiroaki Mano et al. show that brain-specific homeobox, Bsx, is a regulator in pineal gland development. They show that Bsx depletion in zebrafish reduces the expression of a pineal-specific gene responsible for photoreception, affecting the identity of pineal photoreceptive neurons.
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ISSN:2399-3642
2399-3642
DOI:10.1038/s42003-019-0613-1