An annotated chromosome-level genome for the red-fronted brown lemur (Eulemur rufifrons) sheds light on brown lemur evolution

Research output: Contribution to journalArticlepeer-review

Abstract

The red-fronted brown lemur (Eulemur rufifrons) is an important species to the function of Madagascar’s ecosystems, contributing to critical ecological processes such as seed dispersal. Given its ecological, as well as cultural, importance, genomic resources for E. rufifrons are valuable for understanding evolutionary history and informing conservation strategies. In this study, we present an annotated chromosome-level genome assembly for E. rufifrons, generated using PacBio HiFi long reads and Hi-C proximity ligation data, and demonstrate its utility for understanding patterns of divergence among members of the genus Eulemur. The chromosome-level genome size is 2.41 Gb, and it exhibits high-quality metrics including a scaffold N50 of 100.8 Mb and a BUSCO completeness score of 95.3%. Comparative analyses reveal remarkable synteny between our E. rufifrons assembly and the previously published Eulemur mongoz genome, despite an estimated divergence of ∼4 million years. Phylogenetic and network analyses identify pervasive signals of gene flow across Eulemur, with our focal individual showing unexpected genomic affinities to Eulemur rufus, highlighting the need for methods that account for reticulation in phylogenomic studies. Overall, this genome for E. rufifrons provides a valuable resource for exploring lemur evolutionary history, genomic divergence, and patterns of hybridization. Future research should leverage chromosome-level assemblies to investigate gene flow, adaptive introgression, and regions under selection, advancing our understanding of lemur diversity and informing conservation strategies for these imperiled primates.

Original languageEnglish
Article numberjkaf213
Pages (from-to)1-12
Number of pages12
JournalG3: Genes, Genomes, Genetics
Volume15
Issue number11
DOIs
StatePublished - Nov 12 2025

Bibliographical note

Publisher Copyright:
© The Author(s) 2025.

Funding

We are grateful to the Duke Lemur Center (DLC) for making available its genomic resources and we thank the DLC’s Director of Research Erin Ehmke, Gabbi Hirschkorn, and the DLC staff for facilitating the collection and transfer of tissue from Redbay. We also thank Katie Carter and Mark Dasenko at Oregon State University’s Center for Quantitative Life Sciences core lab facility and staff at the University of Oregon’s Genomics and Cell Characterization Core Facility for their assistance with sequencing and lab work. This work was supported by the U.S. National Science Foundation (DEB-2207198), including a Career-Life Balance Supplement. Conflicts of interest. None declared. This work was supported by the U.S. National Science Foundation (DEB-2207198), including a Career-Life Balance Supplement. Conflicts of interest. None declared.

FundersFunder number
Duke Lemur Center
Oregon State University
National Science Foundation Arctic Social Science ProgramDEB-2207198

    Keywords

    • Hi-C
    • Madagascar
    • Pacific biosciences
    • conservation
    • genome assembly
    • lemur

    ASJC Scopus subject areas

    • Molecular Biology
    • Genetics
    • Genetics(clinical)

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