The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions
Epithelial apico-basal polarity is established through the asymmetric cortical distribution of the Par, Crumbs and Scribble polarity modules. Apical (Par and Crumbs) and basolateral (Scribble) polarity modules overlap at the apical-lateral border, which, in mammals, is defined by the apical junction...
Saved in:
Main Authors: | , , , , , |
---|---|
Other Authors: | |
Format: | Article |
Language: | English |
Published: |
2020
|
Subjects: | |
Online Access: | https://hdl.handle.net/10356/143166 https://doi.org/10.21979/N9/TFWJFO |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Institution: | Nanyang Technological University |
Language: | English |
id |
sg-ntu-dr.10356-143166 |
---|---|
record_format |
dspace |
spelling |
sg-ntu-dr.10356-1431662023-02-28T17:08:28Z The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions Tan, Benedict Siti Maryam J. M. Yatim Peng, Suat Gunaratne, Jayantha Hunziker, Walter Ludwig, Alexander School of Biological Sciences NTU Institute of Structural Biology Science::Biological sciences Par3 Pals1 Epithelial apico-basal polarity is established through the asymmetric cortical distribution of the Par, Crumbs and Scribble polarity modules. Apical (Par and Crumbs) and basolateral (Scribble) polarity modules overlap at the apical-lateral border, which, in mammals, is defined by the apical junctional complex (AJC). The AJC is composed of tight junctions (TJ) and adherens junctions (AJ) and plays fundamental roles in epithelial morphogenesis and plasticity. However, the molecular composition and precise sub-junctional organization of the AJC and its associated polarity regulators are not well defined. Here, we used the peroxidase APEX2 for quantitative proximity proteomics (QPP) and electron microscopy (EM) imaging to dissect the architecture of the AJC in fully polarized MDCK-II cells. We present a high-confidence proteome of the apical-lateral border in which TJ and AJ components and apical and lateral compartment markers are spatially resolved. We further demonstrate that the Crumbs complex (Pals1, PatJ, Lin7c, and Crumbs3) defines a hitherto unidentified membrane compartment apical of TJ, which we coin the vertebrate marginal zone (VMZ). QPP, imaging, and immunoprecipitation assays showed that the HOMER scaffolding proteins, PKN2 and PTPN13, and the membrane-proximal HIPPO pathway proteins ARHGAP29 and STXBP4 are recruited to the VMZ via the PDZ domains of PatJ. Taken together, our work defines the spatial and molecular organization of the apical-lateral border in mammalian epithelial cells, reveals an intriguing molecular and spatial conservation of invertebrate and vertebrate cell polarity protein domains, and identifies a VMZ-associated protein network implicated in HIPPO signaling and the control of the cortical actin cytoskeleton. Agency for Science, Technology and Research (A*STAR) Accepted version We thank Andre le Bivic, Spiros Efthimiopoulos, Ben Margolis, Jingshi Shen, Karl Matter, and Ceniz Zihni for providing antibodies, plasmids, and other reagents. This work was supported by an NTU Singapore start-up-grant to A.L. and by funding from the Agency for Science and Technology (A*STAR), Singapore, to W.H. and J.G. We thank Sara Sandin and Tom Carney for supporting this work through research grants RG39/14 and NIM/03/2016. B.T. was a recipient of a PhD scholarship from the A*STAR Graduate Academy. We further thank the NTU Institute of Structural Biology (NISB) for support. 2020-08-07T02:45:26Z 2020-08-07T02:45:26Z 2020 Journal Article Tan, B., Siti Maryam J. M. Yatim, Peng, S., Gunaratne, J., Hunziker, W., & Ludwig, A. (2020). The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions. Current Biology, 30(14), 2791-2804. doi:10.1016/j.cub.2020.05.032 0960-9822 https://hdl.handle.net/10356/143166 10.1016/j.cub.2020.05.032 14 30 2791 2804 en Current Biology https://doi.org/10.21979/N9/TFWJFO © 2020 Elsevier Inc. All rights reserved. This paper was published in Current Biology and is made available with permission of Elsevier Inc. application/vnd.ms-excel application/pdf |
institution |
Nanyang Technological University |
building |
NTU Library |
continent |
Asia |
country |
Singapore Singapore |
content_provider |
NTU Library |
collection |
DR-NTU |
language |
English |
topic |
Science::Biological sciences Par3 Pals1 |
spellingShingle |
Science::Biological sciences Par3 Pals1 Tan, Benedict Siti Maryam J. M. Yatim Peng, Suat Gunaratne, Jayantha Hunziker, Walter Ludwig, Alexander The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
description |
Epithelial apico-basal polarity is established through the asymmetric cortical distribution of the Par, Crumbs and Scribble polarity modules. Apical (Par and Crumbs) and basolateral (Scribble) polarity modules overlap at the apical-lateral border, which, in mammals, is defined by the apical junctional complex (AJC). The AJC is composed of tight junctions (TJ) and adherens junctions (AJ) and plays fundamental roles in epithelial morphogenesis and plasticity. However, the molecular composition and precise sub-junctional organization of the AJC and its associated polarity regulators are not well defined. Here, we used the peroxidase APEX2 for quantitative proximity proteomics (QPP) and electron microscopy (EM) imaging to dissect the architecture of the AJC in fully polarized MDCK-II cells. We present a high-confidence proteome of the apical-lateral border in which TJ and AJ components and apical and lateral compartment markers are spatially resolved. We further demonstrate that the Crumbs complex (Pals1, PatJ, Lin7c, and Crumbs3) defines a hitherto unidentified membrane compartment apical of TJ, which we coin the vertebrate marginal zone (VMZ). QPP, imaging, and immunoprecipitation assays showed that the HOMER scaffolding proteins, PKN2 and PTPN13, and the membrane-proximal HIPPO pathway proteins ARHGAP29 and STXBP4 are recruited to the VMZ via the PDZ domains of PatJ. Taken together, our work defines the spatial and molecular organization of the apical-lateral border in mammalian epithelial cells, reveals an intriguing molecular and spatial conservation of invertebrate and vertebrate cell polarity protein domains, and identifies a VMZ-associated protein network implicated in HIPPO signaling and the control of the cortical actin cytoskeleton. |
author2 |
School of Biological Sciences |
author_facet |
School of Biological Sciences Tan, Benedict Siti Maryam J. M. Yatim Peng, Suat Gunaratne, Jayantha Hunziker, Walter Ludwig, Alexander |
format |
Article |
author |
Tan, Benedict Siti Maryam J. M. Yatim Peng, Suat Gunaratne, Jayantha Hunziker, Walter Ludwig, Alexander |
author_sort |
Tan, Benedict |
title |
The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
title_short |
The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
title_full |
The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
title_fullStr |
The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
title_full_unstemmed |
The mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
title_sort |
mammalian crumbs complex defines a distinct polarity domain apical of epithelial tight junctions |
publishDate |
2020 |
url |
https://hdl.handle.net/10356/143166 https://doi.org/10.21979/N9/TFWJFO |
_version_ |
1759857160987082752 |