Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-5260
Authors: Sorusch, Nasrin
Yildirim, Adem
Knapp, Barbara
Janson, Julia
Fleck, Wiebke
Scharf, Caroline
Wolfrum, Uwe
Title: SANS (USH1G) molecularly links the human Usher syndrome protein network to the intraflagellar transport module by direct binding to IFT-B proteins
Online publication date: 27-Oct-2020
Language: english
Abstract: The human Usher syndrome (USH) is a retinal ciliopathy, characterized by profound congenital deafness, variable vestibular dysfunction and pre-pubertal onset of retinitis pigmentosa. In the effected sensory cells, USH protein networks are assumed to function in ciliary transport processes. The USH1G protein SANS is a scaffold of the ciliary/periciliary USH protein network of photoreceptor cells. Moreover, SANS is associated with microtubules, the transport routes for protein delivery toward the cilium. To enlighten the role of SANS in ciliary transport processes, we aimed to identify transport related proteins associated with SANS. The intraflagellar transport (IFT) system is a conserved mechanism for bi-directional transport toward and through primary cilia. Thus, we tested the direct binding of SANS to IFT molecules, namely IFT20, IFT57, and IFT74 in 1:1 yeast-two-hybrid assay. The identified SANS-IFT interactions were validated in vitro via independent complementary interaction assays and in cells by applying membrane targeting assays. Quantitative immunofluorescence microscopy revealed the co-localization of SANS with IFT20, IFT52, and IFT57 particularly at ciliary base of wild type mouse photoreceptor cells. Analysis of photoreceptor cells of SANS knock out mice revealed the decrease of IFTs in the ciliary compartment indicating a role of SANS in the proper positioning of IFT-B molecules in primary cilia. Our study demonstrated direct binding of IFT complex B proteins IFT52 and IFT57 to the N-terminal ankyrin repeats and the central domain of SANS. Our data also indicate that pathologic mutations in the N-terminus of SANS lead to the loos of SANS binding to IFT-B molecules. Our findings provide direct evidence for a molecular link between the ciliary USH protein network and the IFT transport module in primary cilia.
DDC: 570 Biowissenschaften
570 Life sciences
Institution: Johannes Gutenberg-Universität Mainz
Department: FB 10 Biologie
Place: Mainz
DOI: http://doi.org/10.25358/openscience-5260
Version: Published version
Publication type: Zeitschriftenaufsatz
License: CC BY
Information on rights of use: https://creativecommons.org/licenses/by/4.0/
Journal: Frontiers in cell and developmental biology
7
Pages or article number: Art. 216
Publisher: Frontiers Media
Publisher place: Lausanne
Issue date: 2019
ISSN: 2296-634X
Publisher URL: https://doi.org/10.3389/fcell.2019.00216
Publisher DOI: 10.3389/fcell.2019.00216
Appears in collections:JGU-Publikationen

Files in This Item:
  File Description SizeFormat
Thumbnail
sorusch_nasrin-sans_(ush1g)_m-20201027092115642.pdf4.02 MBAdobe PDFView/Open