Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium

Summary Development of epithelial cell polarity is a highly dynamic process, and often established by the sequential recruitment of conserved protein complexes, such as the Par or the Crumbs (Crb) complex. However, detailed insights into the refinement of polarity and the formation of the complexes...

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Main Authors: Marta Luz, Elisabeth Knust
Format: Article
Language:English
Published: The Company of Biologists 2013-07-01
Series:Biology Open
Subjects:
Online Access:http://bio.biologists.org/content/2/9/867
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spelling doaj-654042a1c685473e94cfede5509e3ffd2021-06-02T09:07:24ZengThe Company of BiologistsBiology Open2046-63902013-07-012986787110.1242/bio.2013537120135371Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epitheliumMarta LuzElisabeth KnustSummary Development of epithelial cell polarity is a highly dynamic process, and often established by the sequential recruitment of conserved protein complexes, such as the Par or the Crumbs (Crb) complex. However, detailed insights into the refinement of polarity and the formation of the complexes are still lacking. Here, we established fluorescently tagged Lin7c, a core member of the Crb complex, as an ideal tool to follow development of polarity in zebrafish epithelia. We find that in gastrula stages, RFP-Lin7c is found in the cytosol of the enveloping layer, while Pard3-GFP is already polarized at this stage. During development of the retinal epithelium, RFP-Lin7c localization is refined from being cytosolic at 14 hours post fertilization (hpf) to almost entirely apical in cells of the eye cup at 28 hpf. This apical Lin7c localization depends on the Crb complex members Oko meduzy and Nagie oko. Thus, fluorescently tagged Lin7c can be used in a broad range of epithelia to follow polarity maturation in vivo and specifically to elucidate the sequence of events determining Crb complex-mediated polarity.http://bio.biologists.org/content/2/9/867PolarityNeuroepitheliaRetinaCrumbsZebrafish
collection DOAJ
language English
format Article
sources DOAJ
author Marta Luz
Elisabeth Knust
spellingShingle Marta Luz
Elisabeth Knust
Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
Biology Open
Polarity
Neuroepithelia
Retina
Crumbs
Zebrafish
author_facet Marta Luz
Elisabeth Knust
author_sort Marta Luz
title Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
title_short Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
title_full Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
title_fullStr Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
title_full_unstemmed Fluorescently tagged Lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
title_sort fluorescently tagged lin7c is a dynamic marker for polarity maturation in the zebrafish retinal epithelium
publisher The Company of Biologists
series Biology Open
issn 2046-6390
publishDate 2013-07-01
description Summary Development of epithelial cell polarity is a highly dynamic process, and often established by the sequential recruitment of conserved protein complexes, such as the Par or the Crumbs (Crb) complex. However, detailed insights into the refinement of polarity and the formation of the complexes are still lacking. Here, we established fluorescently tagged Lin7c, a core member of the Crb complex, as an ideal tool to follow development of polarity in zebrafish epithelia. We find that in gastrula stages, RFP-Lin7c is found in the cytosol of the enveloping layer, while Pard3-GFP is already polarized at this stage. During development of the retinal epithelium, RFP-Lin7c localization is refined from being cytosolic at 14 hours post fertilization (hpf) to almost entirely apical in cells of the eye cup at 28 hpf. This apical Lin7c localization depends on the Crb complex members Oko meduzy and Nagie oko. Thus, fluorescently tagged Lin7c can be used in a broad range of epithelia to follow polarity maturation in vivo and specifically to elucidate the sequence of events determining Crb complex-mediated polarity.
topic Polarity
Neuroepithelia
Retina
Crumbs
Zebrafish
url http://bio.biologists.org/content/2/9/867
work_keys_str_mv AT martaluz fluorescentlytaggedlin7cisadynamicmarkerforpolaritymaturationinthezebrafishretinalepithelium
AT elisabethknust fluorescentlytaggedlin7cisadynamicmarkerforpolaritymaturationinthezebrafishretinalepithelium
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