Evidence map›Paper›PMID 39919095›Full record

ArticlePLoS biology2025

Unprecedented female mutation bias in the aye-aye, a highly unusual lemur from Madagascar.

Richard J Wang, Yadira Peña-García, Muthuswamy Raveendran, R Alan Harris, Thuy-Trang Nguyen, Marie-Claude Gingras, Yifan Wu, Lesette Perez, Anne D Yoder, Joe H Simmons and 2 more

Abstract read
In one paragraph

Article in PLoS biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. EstimatingbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Population size interacts with reproductive longevity to shape the germline mutation rate.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Richard J WangDepartment of Biology, Indiana University, Bloomington, Indiana, United States of America.
Yadira Peña-GarcíaDepartment of Biology, Indiana University, Bloomington, Indiana, United States of America.
Muthuswamy RaveendranHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
R Alan HarrisHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Thuy-Trang NguyenDepartment of Computer Science, Indiana University, Bloomington, Indiana, United States of America.
Marie-Claude GingrasHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Yifan WuHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Lesette PerezHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Anne D YoderDepartment of Biology, Duke University, Durham, North Carolina, United States of America.
Joe H SimmonsKeeling Center for Comparative Medicine and Research, MD Anderson Cancer Center, Bastrop, Texas, United States of America.
Jeffrey RogersHuman Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States of America.
Matthew W HahnDepartment of Biology, Indiana University, Bloomington, Indiana, United States of America.ORCID https://orcid.org/0000-0002-5731-8808

Funding

Specific Pathogen Free Baboon Research Resource (SPFBRR) - Bridge Funding Administrative SupplementP40OD024628 · OD · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Joe H. Simmons · 2017 to 2026
$15.7M
Common Themes in Reproductive DiversityT32HD049336 · NICHD · TRUSTEES OF INDIANA UNIVERSITY · PI DALE R SENGELAUB · 2005 to 2026
$4.4M
Dissecting the mechanisms and timing of de novo mutations in primatesR01HD107120 · NICHD · TRUSTEES OF INDIANA UNIVERSITY · PI Matthew William Hahn · 2023 to 2026
$1.5M
NICHD NIH HHS R01 HD107120NICHD NIH HHS T32 HD049336NIH HHS P40 OD024628
6 · The paper itself

Abstract

Every mammal studied to date has been found to have a male mutation bias: male parents transmit more de novo mutations to offspring than female parents, contributing increasingly more mutations with age. Although male-biased mutation has been studied for more than 75 years, its causes are still debated. One obstacle to understanding this pattern is its near universality-without variation in mutation bias, it is difficult to find an underlying cause. Here, we present new data on multiple pedigrees from two primate species: aye-ayes (Daubentonia madagascariensis), a member of the strepsirrhine primates, and olive baboons (Papio anubis). In stark contrast to the pattern found across mammals, we find a much larger effect of maternal age than paternal age on mutation rates in the aye-aye. In addition, older aye-aye mothers transmit substantially more mutations than older fathers. We carry out both computational and experimental validation of our results, contrasting them with results from baboons and other primates using the same methodologies. Further, we analyze a set of DNA repair and replication genes to identify candidate mutations that may be responsible for the change in mutation bias observed in aye-ayes. Our results demonstrate that mutation bias is not an immutable trait, but rather one that can evolve between closely related species. Further work on aye-ayes (and possibly other lemuriform primates) should help to explain the molecular basis for sex-biased mutation.

Indexed as

MutationStrepsirhiniAnimalsFemaleMadagascarMaleMutation RatePapio anubisPedigree

Identifiers

PMID39919095
PMCPMC11819580

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.