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PreprintCC BYbioRxiv

Auxin-inducible degron-mediated protein depletion in Diplonema papillatum

  1. 1University of Edinburgh

Abstract

Diplonemids are highly abundant unicellular flagellates that are evolutionarily divergent from traditional model eukaryotes. Diplonema papillatum is a model diplonemid for which several molecular tools have recently been established. However, no method for conditional protein depletion was available. Here, we have adapted an auxin-inducible degron (AID) system in D. papillatum. Depletion of the KIN-A motor protein (a glycomonad-specific component of the chromosomal passenger complex) causes defects in chromosome segregation and cell proliferation. The AID system also successfully depleted a divergent Mad1 protein that localizes at nuclear pores, and a flagellar component, CFAP20. Our study demonstrates the power of the AID system to perform loss-of-function studies in D. papillatum.

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BibTeX
@misc{clifford2026auxininducible,
  title = {{Auxin-inducible degron-mediated protein depletion in Diplonema papillatum}},
  author = {G. Clifford and B. Akiyoshi},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.11.751042},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.11.751042v1},
  note = {CC BY},
}
RIS
TY  - UNPB
TI  - Auxin-inducible degron-mediated protein depletion in Diplonema papillatum
AU  - G. Clifford
AU  - B. Akiyoshi
PY  - 2026
DA  - 2026/09/11
PB  - bioRxiv
DO  - 10.64898/2026.09.11.751042
UR  - https://www.biorxiv.org/content/10.64898/2026.09.11.751042v1
AB  - Diplonemids are highly abundant unicellular flagellates that are evolutionarily divergent from traditional model eukaryotes. Diplonema papillatum is a model diplonemid for which several molecular tools have recently been established. However, no method for conditional protein depletion was available. Here, we have adapted an auxin-inducible degron (AID) system in D. papillatum. Depletion of the KIN-A motor protein (a glycomonad-specific component of the chromosomal passenger complex) causes defects in chromosome segregation and cell proliferation. The AID system also successfully depleted a divergent Mad1 protein that localizes at nuclear pores, and a flagellar component, CFAP20. Our study demonstrates the power of the AID system to perform loss-of-function studies in D. papillatum.
ER  -