# Divergent Cardiovascular Adaptations and Gene Regulation in High-Elevation Natives and Recent Colonizers of the Qinghai-Tibetan Plateau

**Authors:** Huishang She, Graham R Scott, Yun Fang, Qingshuo Zhao, Fanwei Meng, Yanhua Qu

PMC · DOI: 10.1093/molbev/msaf103 · 2025-05-09

## TL;DR

This study shows that species native to high elevations have different heart adaptations compared to recent arrivals, due to evolutionary differences in gene regulation.

## Contribution

The study reveals a regulatory basis for divergent cardiovascular adaptations in high-elevation species through gene expression differences in a conserved pathway.

## Key findings

- Recent colonizers show cardiac hypertrophy with increased heart mass and cardiomyocyte size.
- Native species have higher capillary density but no cardiac hypertrophy, enhancing oxygen diffusion.
- Differential expression of IRS2 and AKT1 genes explains variation in cardiomyocyte size between native and colonizer species.

## Abstract

High elevation imposes unrelenting and unavoidable hypoxia on species inhabiting these environments, providing an excellent natural setting for studying convergent or divergent evolution. By integrating measures of phenotypic variation, gene regulation, and functional performance, our study demonstrates that recent colonizers of high-elevation environments exhibit fundamentally different cardiovascular changes compared to long-term natives of these environments. Through the studying of heart morphological phenotypes, we showed that recent colonizers exhibit signs of cardiac hypertrophy, reflected by increased relative heart mass (heart mass/body mass) and cardiomyocyte size compared to their low-elevation relatives. In contrast, native species show no signs of cardiac hypertrophy and instead have 3-fold higher capillary densities than the colonizers, a change that likely enhances tissue oxygen diffusing capacity in the former. Using phylogenetic principal component analysis to quantify multivariate trait divergence, we show that native species are similar in cardiovascular phenotype and underlying gene expression, but differ appreciably from recent colonizers. We further demonstrate, using a functional assay, that differential expression of two genes (IRS2 and AKT1) in a conserved regulatory pathway mediates cardiomyocyte hypertrophy, which could explain the observed variation in cardiomyocyte size between native species and recent colonizers. This regulatory basis of variation in cardiac phenotype involves the differential expression of genes in a cardiomyocyte hypertrophy pathway that is conserved across birds, humans and other mammals. Collectively, our study highlights that evolutionary history is a critical determinant of cardiovascular variation in high-elevation environments.

## Linked entities

- **Genes:** IRS2 (insulin receptor substrate 2) [NCBI Gene 8660], AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207]

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, IRS2 (insulin receptor substrate 2) [NCBI Gene 8660] {aka IRS-2}
- **Diseases:** cardiomyocyte hypertrophy (MESH:D006984), hypoxia (MESH:D000860), cardiac hypertrophy (MESH:D006332)
- **Chemicals:** oxygen (MESH:D010100)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12103977/full.md

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Source: https://tomesphere.com/paper/PMC12103977