PUBLICATION

WDR31 displays functional redundancy with GTPase-activating proteins (GAPs) ELMOD and RP2 in regulating IFT complex and recruiting the BBSome to cilium

Authors
Cevik, S., Peng, X., Beyer, T., Pir, M.S., Yenisert, F., Woerz, F., Hoffmann, F., Altunkaynak, B., Pir, B., Boldt, K., Karaman, A., Cakiroglu, M., Oner, S.S., Cao, Y., Ueffing, M., Kaplan, O.I.
ID
ZDB-PUB-230521-34
Date
2023
Source
Life science alliance   6(8): (Journal)
Registered Authors
Cao, Ying
Keywords
none
MeSH Terms
  • Animals
  • Biological Transport
  • Caenorhabditis elegans/metabolism
  • Caenorhabditis elegans Proteins*/metabolism
  • Cilia*/metabolism
  • GTPase-Activating Proteins*/metabolism
  • Zebrafish
  • Zebrafish Proteins*/metabolism
PubMed
37208194 Full text @ Life Sci Alliance
Abstract
The correct intraflagellar transport (IFT) assembly at the ciliary base and the IFT turnaround at the ciliary tip are key for the IFT to perform its function, but we still have poor understanding about how these processes are regulated. Here, we identify WDR31 as a new ciliary protein, and analysis from zebrafish and Caenorhabditis elegans reveals the role of WDR31 in regulating the cilia morphology. We find that loss of WDR-31 together with RP-2 and ELMD-1 (the sole ortholog ELMOD1-3) results in ciliary accumulations of IFT Complex B components and KIF17 kinesin, with fewer IFT/BBSome particles traveling along cilia in both anterograde and retrograde directions, suggesting that the IFT/BBSome entry into the cilia and exit from the cilia are impacted. Furthermore, anterograde IFT in the middle segment travels at increased speed in wdr-31;rpi-2;elmd-1 Remarkably, a non-ciliary protein leaks into the cilia of wdr-31;rpi-2;elmd-1, possibly because of IFT defects. This work reveals WDR31-RP-2-ELMD-1 as IFT and BBSome trafficking regulators.
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