# Adaptive Genetic Variation in Black‐and‐White Snub‐Nosed Monkeys (Rhinopithecus bieti): Low Diversity and the Role of Balancing Selection

**Authors:** Fei Long, Mei‐Jing Ying, Tian‐Qi Shi, Paul A. Garber, Ru‐Liang Pan, Jian‐Dong Lai, Zhi‐Pang Huang, Bao‐Guo Li, Pei Zhang

PMC · DOI: 10.1002/ece3.73070 · Ecology and Evolution · 2026-03-03

## TL;DR

This study examines the low genetic diversity in black-and-white snub-nosed monkeys and its implications for conservation.

## Contribution

The study provides new insights into adaptive genetic variation and balancing selection in an endangered primate species.

## Key findings

- Low heterozygosity and polymorphism were observed in MHC class I exons of Rhinopithecus bieti.
- Positive selection and trans-species polymorphism were detected, indicating balancing selection.
- Low genetic diversity may reduce the species' ability to adapt to environmental changes.

## Abstract

Genetic variation provides the raw material for natural selection, enabling species to maintain adaptive potential, respond to environmental changes, and resist pathogens. Reduced genetic diversity can severely compromise long‐term viability, particularly in small, isolated populations prone to inbreeding, genetic drift, and restricted gene flow—a vicious cycle known as the “extinction vortex”. Assessing genetic diversity in threatened species is therefore critical for effective conservation strategies. The black‐and‐white snub‐nosed monkey (
Rhinopithecus bieti
) is an Endangered primate that has experienced significant population decline and habitat fragmentation, raising concerns about its genetic diversity. We utilized major histocompatibility complex (MHC) class I genes, whose encoded proteins recognize antigens central to immune responses, to assess the adaptive genetic diversity of a semi‐provisioned subpopulation of this species. Species‐specific multi‐locus primers targeting exons 2 and 3 of MHC class I genes were designed using published 
R. bieti
 whole‐genome sequences. Amplicon‐based next‐generation sequencing was employed to genotype these exons in the studied subpopulation inhabiting Baima Snow Mountain National Nature Reserve, Yunnan, China. A total of 16 MHC class I sequences (7 exon 2 sequences and 9 exon 3 sequences) were identified from 47 individuals and assigned to 5 loci. Exon 2 exhibited low heterozygosity (H
e = 0.349) and moderate polymorphism (PIC = 0.281), whereas exon 3 showed extremely low heterozygosity (H
e = 0.147) and low polymorphism (PIC = 0.131). In addition, positive selection signatures were detected in both exons, and phylogenetic analyses indicated trans‐species evolutionary patterns in class I loci. These results underscore the role of balancing selection in maintaining adaptive genetic variation. However, low genetic diversity is likely to have diminished the studied subpopulation's capacity to adapt to environmental change, thereby undermining its long‐term viability. This study emphasizes the urgent need to assess adaptive genetic diversity across all 
R. bieti
 populations in order to develop targeted management strategies. The data generated in this studied subpopulation provide the baseline for comparison.

We investigated the adaptive genetic diversity within a population of Rhinopithecus bieti using amplicon sequencing. From 47 individuals, we identified 16 MHC class I sequences, revealing a low level of adaptive genetic variation. Although evidence for balancing selection, including positive selection and trans‐species polymorphism, was observed, these selective forces did not ameliorate the observed low genetic diversity. Our findings underscore the urgent need to assess adaptive genetic diversity across the species to inform conservation management strategies.

## Linked entities

- **Species:** Rhinopithecus bieti (taxon 61621)

## Full-text entities

- **Genes:** albumin [NCBI Gene 108523438], HLA-DRB1 (major histocompatibility complex, class II, DR beta 1) [NCBI Gene 3123] {aka DRB1, HLA-DR1B, HLA-DRB, SS1}, HLA-C (major histocompatibility complex, class I, C) [NCBI Gene 3107] {aka D6S204, HLA-JY3, HLAC, HLC-C, MHC, PSORS1}, HLA-DRB4 (major histocompatibility complex, class II, DR beta 4) [NCBI Gene 3126] {aka DR4, DRB4, HLA-DR4B, HLA-DRB, HLA-DRB4*}
- **Diseases:** depression (MESH:D003866), hypoxia (MESH:D000860)
- **Chemicals:** DETs (MESH:C068718), DMSO (MESH:D004121), amino acid (MESH:D000596), Tris-HCl (-), water (MESH:D014867), EDTA (MESH:D004492), T (MESH:D014316), NaCl (MESH:D012965)
- **Species:** Rhinopithecus avunculus (Dollman's snub-nosed monkey, species) [taxon 66062], Rhinopithecus strykeri (Burmese snub-nosed monkey, species) [taxon 1194336], Primates (primates, order) [taxon 9443], Homo sapiens (human, species) [taxon 9606], Tupaia belangeri (common tree shrew, species) [taxon 37347], Lyrurus tetrix (black grouse, species) [taxon 1233216], Macaca mulatta (rhesus macaque, species) [taxon 9544], Spheniscus magellanicus (Magellanic penguin, species) [taxon 37081], Papio anubis (baboon, species) [taxon 9555], Rhinopithecus roxellana (golden snub-nosed monkey, species) [taxon 61622], Rhinopithecus brelichi (Gray snub-nosed monkey, species) [taxon 224329], Spheniscus humboldti (Humboldt's penguin, species) [taxon 9240], Rhinopithecus bieti (black snub-nosed monkey, species) [taxon 61621]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12957539/full.md

## References

100 references — full list in the complete paper: https://tomesphere.com/paper/PMC12957539/full.md

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Source: https://tomesphere.com/paper/PMC12957539