Skip to content
DraconiticResearch
Search Sources API
203,234 studies31 sourcesUpdated 46 min ago
PreprintCC BY-NDbioRxiv

Starship transposons mobilise via a circular intermediate with potential biotechnological applications

  1. 1The University of Melbourne

Abstract

Mobile genetic elements drive genome evolution and horizontal gene transfer, yet the mechanisms underlying the mobility of many eukaryotic elements remain poorly understood. Here we show that Starships, a recently discovered class of giant transposable elements in fungi, mobilise via an extrachromosomal circular intermediate. Using deep sequencing, we detect low-abundance reads spanning the hypothesised junction consistent with circularisation. We demonstrate that a synthetic circular intermediate, or "starmid", is sufficient for recombinase-dependent integration into the host genome and that circularisation enhances expression of the starship-encoded tyrosine recombinase through juxtaposition of 3' and 5' terminal sequences. This topology-dependent regulation parallels bacterial integrative elements, in which excision activates recombination machinery. Exploiting this circular intermediate, we explore starmids as a platform for transient DNA delivery, enabling CRISPR Cas9-mediated genome editing in Paecilomyces variotii with subsequent curing of the construct. Together, our results shed light on the biology of starship mobility and suggest promising biotechnology applications for these elements.

Related

  1. Role of transposons in the specialization of Botrytis cinerea to grapevine: Insights into small RNAs and a new Starship
    Antoine Porquier, Adeline Simon, Justine Vergne +11
    BioRxivPreprintCC BY-NC-ND 4.0Full textMolecular biology & gene regulationProteomics & metabolomicsHAL
  2. Actinidin: A Review from Molecular Mechanisms to Biotechnological Applications
    Daniel Castañeda-Valbuena, Olga Tavano, Ángel Berenguer-Murcia +4
    CatalystsPeer-reviewedCC BY 4.0Molecular biology & gene regulationCrossref
  3. Restriction–Modification Systems in Lactic Acid Bacteria: Diversity, Mechanisms, Evolution, and Biotechnological Applications
    Kseniya D. Bondarenko, Alina I. Selimzianova, Oksana V. Berezina +2
    International Journal of Molecular SciencesPeer-reviewedCC BY 4.0General biochemistryCrossref
  4. Transposons as Tools for Future Genome Engineering in Yeasts and Filamentous Fungi
    Bingyin Peng, Masahiro Tominaga, Chengqiang Wang +2
    Yeast (Chichester, England)Peer-reviewedCC BY-NC 4.0Full text1 citedMolecular biology & gene regulationPMC
  5. Arc represses gene expression in IS605-family transposons
    Y. D. Moon, R. Zedaveinyte, T. Wiegand +1
    bioRxivPreprintCC BYFull textMolecular biology & gene regulationbioRxiv
BibTeX
@misc{baericke2026starship,
  title = {{Starship transposons mobilise via a circular intermediate with potential biotechnological applications}},
  author = {A. Baericke and V. Jameson and A. S. Urquhart},
  howpublished = {bioRxiv},
  year = {2026},
  month = sep,
  doi = {10.64898/2026.09.21.753150},
  url = {https://www.biorxiv.org/content/10.64898/2026.09.21.753150v1},
  note = {CC BY-ND},
}
RIS
TY  - UNPB
TI  - Starship transposons mobilise via a circular intermediate with potential biotechnological applications
AU  - A. Baericke
AU  - V. Jameson
AU  - A. S. Urquhart
PY  - 2026
DA  - 2026/09/21
PB  - bioRxiv
DO  - 10.64898/2026.09.21.753150
UR  - https://www.biorxiv.org/content/10.64898/2026.09.21.753150v1
AB  - Mobile genetic elements drive genome evolution and horizontal gene transfer, yet the mechanisms underlying the mobility of many eukaryotic elements remain poorly understood. Here we show that Starships, a recently discovered class of giant transposable elements in fungi, mobilise via an extrachromosomal circular intermediate. Using deep sequencing, we detect low-abundance reads spanning the hypothesised junction consistent with circularisation. We demonstrate that a synthetic circular intermediate, or "starmid", is sufficient for recombinase-dependent integration into the host genome and that circularisation enhances expression of the starship-encoded tyrosine recombinase through juxtaposition of 3' and 5' terminal sequences. This topology-dependent regulation parallels bacterial integrative elements, in which excision activates recombination machinery. Exploiting this circular intermediate, we explore starmids as a platform for transient DNA delivery, enabling CRISPR Cas9-mediated genome editing in Paecilomyces variotii with subsequent curing of the construct. Together, our results shed light on the biology of starship mobility and suggest promising biotechnology applications for these elements.
ER  -