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Published November 28, 2023 | in press
Journal Article Open

Aneuploidy during development in facultative parthenogenetic Drosophila

  • 1. ROR icon California Institute of Technology

Abstract

From concatenated chromosomes to polyploidization, large-scale genome changes are known to occur in parthenogenetic animals. Here, we report mosaic aneuploidy in larval brains of facultatively parthenogenetic Drosophila. We identified a background of aneuploidy in D. mercatorum strains and found increased levels of aneuploidy in the larval brain tissue of animals arising parthenogenetically versus those arising from sexual reproduction. There is also intra-individual variation in germline-derived aneuploidy within the same strain. To determine if this is a general feature of facultative parthenogenesis in drosophilids, we compared sexually reproduced and parthenogenetic offspring from an engineered facultative parthenogenetic strain of D. melanogaster. In addition to germline-derived aneuploidy, this revealed somatic aneuploidy that increased by up to fourfold in parthenogens compared to sexually reproduced offspring. Therefore, the genetic combination identified in D. mercatorum that causes facultative parthenogenesis in D. melanogaster results in aneuploidy, which indicates that the loss of mitotic control resulting in parthenogenesis causes subsequent genome variation within the parthenogenetic offspring. Our findings challenge the assumption that parthenogenetic offspring are near genetic replicas of their mothers.

Copyright and License

© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Acknowledgement

We would like to thank Jose Casal for reading the manuscript and discussions about the work. We would like to thank Paula Almeida-Coelho for technical advice on in situs and karyotyping. We are grateful to the Genetics Fly Facility for their support of this work. The work was supported by the Leverhulme Trust Project Grant RPG-2018-229 and the Wellcome Trust Institutional Strategic Support Fund (RG89305) for DMG and ALS.

Contributions

ALS designed and conducted all experiments and performed all analysis. ALS wrote the manuscript. DMG edited the manuscript. ALS and DMG both procured the funding.

Conflict of Interest

The authors declare no competing interests.

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Additional details

Created:
December 4, 2023
Modified:
January 9, 2024