Published November 15, 2022 | Version Published + Supplemental Material
Journal Article Open

Targeting Drosophila Sas6 to mitochondria reveals its high affinity for Gorab

  • 1. ROR icon California Institute of Technology

Abstract

The ability to relocalize proteins to defined subcellular locations presents a powerful tool to examine protein-protein interactions that can overcome a tendency of non-targeted exogenous proteins to form inaccessible aggregates. Here, we show that a 24-amino-acid sequence from the Drosophila proapoptotic protein Hid's tail anchor (HTA) domain can target exogenous proteins to the mitochondria in Drosophila cells. We use this HTA tag to target the Drosophila centriole cartwheel protein Sas6 to the mitochondria, and show that both exogenous and endogenous Gorab can be co-recruited from the Golgi to the new mitochondrial site. This accords with our previous observation that monomeric Drosophila Gorab binds Sas6 to become centriole associated with a 50-fold greater affinity than dimeric Gorab binds Rab6 to become localized at the Golgi. Strikingly, Drosophila Sas6 can bind both Drosophila Gorab and its human GORAB ortholog, whereas human SAS6 is unable to bind either GORAB or Gorab. We discuss these findings in relation to the evolutionary conservation of Gorab and the divergence of Sas6, possibly reflecting known differences in persistence of the cartwheel in the centriole duplication cycle of fly and human cells.

Additional Information

© 2022. Published by The Company of Biologists Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. This work was funded by National Institutes of Health grants R01 NS119614 and R01 NS113930 awarded to D.M.G. Open Access funding provided by California Institute of Technology. Deposited in PMC for immediate release. Author contributions. Conceptualization: L.K., A.F., D.M.G.; Methodology: L.K., A.F.; Validation: L.K., A.F., D.M.G.; Formal analysis: L.K., A.F.; Investigation: L.K., A.F.; Resources: D.M.G.; Data curation: L.K.; Writing - original draft: L.K., D.M.G.; Writing - review & editing: L.K., D.M.G.; Visualization: L.K.; Supervision: D.M.G.; Project administration: D.M.G.; Funding acquisition: D.M.G. The authors declare no competing or financial interests.

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Published - biolopen-11-059545.pdf

Supplemental Material - bio059545supp.pdf

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Additional details

Identifiers

PMCID
PMC9836085
Eprint ID
119605
Resolver ID
CaltechAUTHORS:20230301-701033500.4

Funding

NIH
R01 NS119614
NIH
R01 NS113930
Caltech

Dates

Created
2023-05-08
Created from EPrint's datestamp field
Updated
2023-07-06
Created from EPrint's last_modified field

Caltech Custom Metadata