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Drosophila R8 photoreceptor cell subtype specification requires hibris

Cell differentiation and cell fate determination in sensory systems are essential for stimulus discrimination and coding of environmental stimuli. Color vision is based on the differential color sensitivity of retinal photoreceptors, however the developmental programs that control photoreceptor cell...

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Autores principales: Tan, Hong, Fulton, Ruth E., Chou, Wen-Hai, Birkholz, Denise A., Mannino, Meridee P., Yamaguchi, David M., Aldrich, John C., Jacobsen, Thomas L., Britt, Steven G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556441/
https://www.ncbi.nlm.nih.gov/pubmed/33052948
http://dx.doi.org/10.1371/journal.pone.0240451
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author Tan, Hong
Fulton, Ruth E.
Chou, Wen-Hai
Birkholz, Denise A.
Mannino, Meridee P.
Yamaguchi, David M.
Aldrich, John C.
Jacobsen, Thomas L.
Britt, Steven G.
author_facet Tan, Hong
Fulton, Ruth E.
Chou, Wen-Hai
Birkholz, Denise A.
Mannino, Meridee P.
Yamaguchi, David M.
Aldrich, John C.
Jacobsen, Thomas L.
Britt, Steven G.
author_sort Tan, Hong
collection PubMed
description Cell differentiation and cell fate determination in sensory systems are essential for stimulus discrimination and coding of environmental stimuli. Color vision is based on the differential color sensitivity of retinal photoreceptors, however the developmental programs that control photoreceptor cell differentiation and specify color sensitivity are poorly understood. In Drosophila melanogaster, there is evidence that the color sensitivity of different photoreceptors in the compound eye is regulated by inductive signals between cells, but the exact nature of these signals and how they are propagated remains unknown. We conducted a genetic screen to identify additional regulators of this process and identified a novel mutation in the hibris gene, which encodes an irre cell recognition module protein (IRM). These immunoglobulin super family cell adhesion molecules include human KIRREL and nephrin (NPHS1). hibris is expressed dynamically in the developing Drosophila melanogaster eye and loss-of-function mutations give rise to a diverse range of mutant phenotypes including disruption of the specification of R8 photoreceptor cell diversity. We demonstrate that hibris is required within the retina, and that hibris over-expression is sufficient to disrupt normal photoreceptor cell patterning. These findings suggest an additional layer of complexity in the signaling process that produces paired expression of opsin genes in adjacent R7 and R8 photoreceptor cells.
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spelling pubmed-75564412020-10-21 Drosophila R8 photoreceptor cell subtype specification requires hibris Tan, Hong Fulton, Ruth E. Chou, Wen-Hai Birkholz, Denise A. Mannino, Meridee P. Yamaguchi, David M. Aldrich, John C. Jacobsen, Thomas L. Britt, Steven G. PLoS One Research Article Cell differentiation and cell fate determination in sensory systems are essential for stimulus discrimination and coding of environmental stimuli. Color vision is based on the differential color sensitivity of retinal photoreceptors, however the developmental programs that control photoreceptor cell differentiation and specify color sensitivity are poorly understood. In Drosophila melanogaster, there is evidence that the color sensitivity of different photoreceptors in the compound eye is regulated by inductive signals between cells, but the exact nature of these signals and how they are propagated remains unknown. We conducted a genetic screen to identify additional regulators of this process and identified a novel mutation in the hibris gene, which encodes an irre cell recognition module protein (IRM). These immunoglobulin super family cell adhesion molecules include human KIRREL and nephrin (NPHS1). hibris is expressed dynamically in the developing Drosophila melanogaster eye and loss-of-function mutations give rise to a diverse range of mutant phenotypes including disruption of the specification of R8 photoreceptor cell diversity. We demonstrate that hibris is required within the retina, and that hibris over-expression is sufficient to disrupt normal photoreceptor cell patterning. These findings suggest an additional layer of complexity in the signaling process that produces paired expression of opsin genes in adjacent R7 and R8 photoreceptor cells. Public Library of Science 2020-10-14 /pmc/articles/PMC7556441/ /pubmed/33052948 http://dx.doi.org/10.1371/journal.pone.0240451 Text en © 2020 Tan et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Tan, Hong
Fulton, Ruth E.
Chou, Wen-Hai
Birkholz, Denise A.
Mannino, Meridee P.
Yamaguchi, David M.
Aldrich, John C.
Jacobsen, Thomas L.
Britt, Steven G.
Drosophila R8 photoreceptor cell subtype specification requires hibris
title Drosophila R8 photoreceptor cell subtype specification requires hibris
title_full Drosophila R8 photoreceptor cell subtype specification requires hibris
title_fullStr Drosophila R8 photoreceptor cell subtype specification requires hibris
title_full_unstemmed Drosophila R8 photoreceptor cell subtype specification requires hibris
title_short Drosophila R8 photoreceptor cell subtype specification requires hibris
title_sort drosophila r8 photoreceptor cell subtype specification requires hibris
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7556441/
https://www.ncbi.nlm.nih.gov/pubmed/33052948
http://dx.doi.org/10.1371/journal.pone.0240451
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