GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base

  1. Dong Gil Jang
  2. Keun Yeong Kwon
  3. Yeong Cheon Kweon
  4. Byung-gyu Kim
  5. Kyungjae Myung
  6. Hyun-Shik Lee
  7. Chan Young Park
  8. Taejoon Kwon  Is a corresponding author
  9. Tae Joo Park  Is a corresponding author
  1. Ulsan National Institute of Science and Technology, Republic of Korea
  2. Institute for Basic Science, Republic of Korea
  3. Kyungpook National University, Republic of Korea

Abstract

The gap junction complex functions as a transport channel across the membrane. Among gap junction subunits, gap junction protein α1 (GJA1) is the most commonly expressed subunit. A recent study showed that GJA1 is necessary for the maintenance of motile cilia; however, the molecular mechanism and function of GJA1 in ciliogenesis remain unknown. Here, we examined the functions of GJA1 during ciliogenesis in human retinal pigment epithelium-1 and Xenopus laevis embryonic multiciliated-cells. GJA1 localizes to the motile ciliary axonemes or pericentriolar regions beneath the primary cilium. GJA1 depletion caused malformation of both the primary cilium and motile cilia. Further study revealed that GJA1 depletion affected several ciliary proteins such as BBS4, CP110, and Rab11 in the pericentriolar region and basal body. Interestingly, CP110 removal from the mother centriole was significantly reduced by GJA1 depletion. Importantly, Rab11, a key regulator during ciliogenesis, was immunoprecipitated with GJA1, and GJA1 knockdown caused the mislocalization of Rab11. These findings suggest that GJA1 regulates ciliogenesis by interacting with the Rab11-Rab8 ciliary trafficking pathway.

Data availability

All data generated or analysed during this study are included in the manuscript, supporting file and source data files

The following data sets were generated
    1. Jang D
    2. Park T
    (2022) GJA1 IP/MS dataset
    Dryad Digital Repository, doi:10.5061/dryad.tht76hdxt.

Article and author information

Author details

  1. Dong Gil Jang

    Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  2. Keun Yeong Kwon

    Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  3. Yeong Cheon Kweon

    Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  4. Byung-gyu Kim

    Center for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  5. Kyungjae Myung

    Center for Genomic Integrity, Institute for Basic Science, Ulsan, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  6. Hyun-Shik Lee

    School of Life Sciences, Kyungpook National University, Daegu, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  7. Chan Young Park

    Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea
    Competing interests
    The authors declare that no competing interests exist.
  8. Taejoon Kwon

    Department of Biomedical Engineering, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea
    For correspondence
    tkwon@unist.ac.kr
    Competing interests
    The authors declare that no competing interests exist.
  9. Tae Joo Park

    Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, Republic of Korea
    For correspondence
    parktj@unist.ac.kr
    Competing interests
    The authors declare that no competing interests exist.
    ORCID icon "This ORCID iD identifies the author of this article:" 0000-0003-3176-177X

Funding

Korea National Research Foundation (2021R1A2B5B02002285)

  • Tae Joo Park

Institute for Basic Science (IBS-R001-D1)

  • Taejoon Kwon

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Ethics

Animal experimentation: All animal experiments were performed with appropriate ethical approval from the UNIST Institutional Animal Care and Use Committee (UNISTIACUC-19-22, UNISTIACUC-20-26).

Copyright

© 2022, Jang et al.

This article is distributed under the terms of the Creative Commons Attribution License permitting unrestricted use and redistribution provided that the original author and source are credited.

Metrics

  • 1,196
    views
  • 333
    downloads
  • 3
    citations

Views, downloads and citations are aggregated across all versions of this paper published by eLife.

Download links

A two-part list of links to download the article, or parts of the article, in various formats.

Downloads (link to download the article as PDF)

Open citations (links to open the citations from this article in various online reference manager services)

Cite this article (links to download the citations from this article in formats compatible with various reference manager tools)

  1. Dong Gil Jang
  2. Keun Yeong Kwon
  3. Yeong Cheon Kweon
  4. Byung-gyu Kim
  5. Kyungjae Myung
  6. Hyun-Shik Lee
  7. Chan Young Park
  8. Taejoon Kwon
  9. Tae Joo Park
(2022)
GJA1 depletion causes ciliary defects by affecting Rab11 trafficking to the ciliary base
eLife 11:e81016.
https://doi.org/10.7554/eLife.81016

Share this article

https://doi.org/10.7554/eLife.81016

Further reading

    1. Cell Biology
    2. Chromosomes and Gene Expression
    Bethany M Bartlett, Yatendra Kumar ... Wendy A Bickmore
    Research Article

    During oncogene-induced senescence there are striking changes in the organisation of heterochromatin in the nucleus. This is accompanied by activation of a pro-inflammatory gene expression programme - the senescence associated secretory phenotype (SASP) - driven by transcription factors such as NF-κB. The relationship between heterochromatin re-organisation and the SASP has been unclear. Here we show that TPR, a protein of the nuclear pore complex basket required for heterochromatin re-organisation during senescence, is also required for the very early activation of NF-κB signalling during the stress-response phase of oncogene-induced senescence. This is prior to activation of the SASP and occurs without affecting NF-κB nuclear import. We show that TPR is required for the activation of innate immune signalling at these early stages of senescence and we link this to the formation of heterochromatin-enriched cytoplasmic chromatin fragments thought to bleb off from the nuclear periphery. We show that HMGA1 is also required for cytoplasmic chromatin fragment formation. Together these data suggest that re-organisation of heterochromatin is involved in altered structural integrity of the nuclear periphery during senescence, and that this can lead to activation of cytoplasmic nucleic acid sensing, NF-κB signalling, and activation of the SASP.

    1. Cell Biology
    2. Neuroscience
    Lizbeth de La Cruz, Derek Bui ... Oscar Vivas
    Research Article

    Overactivity of the sympathetic nervous system is a hallmark of aging. The cellular mechanisms behind this overactivity remain poorly understood, with most attention paid to likely central nervous system components. In this work, we hypothesized that aging also affects the function of motor neurons in the peripheral sympathetic ganglia. To test this hypothesis, we compared the electrophysiological responses and ion-channel activity of neurons isolated from the superior cervical ganglia of young (12 weeks), middle-aged (64 weeks), and old (115 weeks) mice. These approaches showed that aging does impact the intrinsic properties of sympathetic motor neurons, increasing spontaneous and evoked firing responses. A reduction of M current emerged as a major contributor to age-related hyperexcitability. Thus, it is essential to consider the effect of aging on motor components of the sympathetic reflex as a crucial part of the mechanism involved in sympathetic overactivity.