The evolutionary origins of the parthenogenetic lizard Aspidoscelis tesselatus

Most vertebrate species reproduce sexually. The whiptail lizards (Aspidoscelis) are a notable exception; at least 11 of the 45 recognized species are parthenogenetic. Here, we focus on one such species (Aspidoscelis tesselatus) as a case study to understand how parthenogenetic species originate and evolve. Using genome-wide sequence data and ecological niche modelling, we find that A. tesselatus likely arose from a single hybrid speciation event between A. scalaris and A. marmoratus less than 500,000 years ago. The geographic ranges of A. tesselatus and its parental species overlap currently, and niche modelling shows this zone of sympatry was even broader during the period when A. tesselatus likely formed. We additionally show evidence that A. tesselatus has a dynamic genome post-formation, with de novo mutations, introgression, and double-strand break associated events all contributing to variation within the species. These results show that asexual lineages can continue to be shaped by ongoing genomic and ecological dynamics, illuminating the processes that influence transitions in reproductive mode.

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Publication Details

Journal
Journal of Heredity
Published
2026-09-15
DOI
https://doi.org/10.1093/jhered/esag077
Primary Topic
Evolution and Genetic Dynamics
Type
article
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article

The evolutionary origins of the parthenogenetic lizard Aspidoscelis tesselatus

Adam D. Leaché, Samuel R. Fisher, Alexander S. Hall, Danielle Rivera et al.
Journal of Heredity
Evolution and Genetic Dynamics
article

The evolutionary origins of the parthenogenetic lizard Aspidoscelis tesselatus

Adam D. Leaché, Samuel R. Fisher, Alexander S. Hall, Danielle Rivera, Corey E. Roelke, Maggie R. Grundler, Sonal Singhal, Matthew K. Fujita, Adrián Nieto‐Montes de, Kathleen Currie
article en

Abstract

Most vertebrate species reproduce sexually. The whiptail lizards (Aspidoscelis) are a notable exception; at least 11 of the 45 recognized species are parthenogenetic. Here, we focus on one such species (Aspidoscelis tesselatus) as a case study to understand how parthenogenetic species originate and evolve. Using genome-wide sequence data and ecological niche modelling, we find that A. tesselatus likely arose from a single hybrid speciation event between A. scalaris and A. marmoratus less than 500,000 years ago. The geographic ranges of A. tesselatus and its parental species overlap currently, and niche modelling shows this zone of sympatry was even broader during the period when A. tesselatus likely formed. We additionally show evidence that A. tesselatus has a dynamic genome post-formation, with de novo mutations, introgression, and double-strand break associated events all contributing to variation within the species. These results show that asexual lineages can continue to be shaped by ongoing genomic and ecological dynamics, illuminating the processes that influence transitions in reproductive mode.

Journal of Heredity
Museum of Vertebrate Zoology (US), The University of Texas at Arlington (US), Dryad Digital Repository (US), California State University, Dominguez Hills (US), Burke Museum of Natural History and Culture (US), Thermo Fisher Scientific (United States) (US), Thermo Fisher Scientific (Israel) (IL), Universidad Nacional Autónoma de México (MX)
Life in Land
Openalex Percentile: Top 11%
Evolution and Genetic Dynamics
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