# Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia

**Authors:** Qianqian Zhang, Jialong Li, Haoyang Huang, Xuan Shang, Yuhua Ye, Wei Zhang, Peng Lin, Yi Gong, Boon-Peng Hoh, Qingming Luo, Tizhen Yan, Xinghua Pan, Mark Stoneking, Shuhua Xu, Xiangmin Xu, Lian Deng

PMC · DOI: 10.1038/s41467-025-65019-0 · Nature Communications · 2025-11-20

## TL;DR

The study reveals that β-thalassemia mutations in southern East Asia have multiple origins shaped by agriculture, migration, and selection.

## Contribution

The paper identifies three haplotype groups and traces mutation origins to agricultural expansions and migrations in southern China.

## Key findings

- CD41/42 mutation originated in mainland China during agricultural expansions over 7420 years ago.
- The -50 mutation likely began on Hainan Island and spread to the mainland.
- HbE shows bidirectional spread between southern China and South/Southeast Asia.

## Abstract

Over 400 β-thalassemia mutations show population-differentiated spectra, yet their origins and evolution remain unclear. Focusing on targeted sequencing of 20,222 individuals and 510 β-thalassemia patients in southern China, we identified three major haplotype groups (HG) at the β-globin locus and observed highest haplotype diversity for CD41/42, -50, and HbE among 13 prevalent mutations in 993 carriers. Allele dating suggest these mutations emerged during agricultural expansions in the past 7420 years, represented by CD41/42 arising in mainland China. However, the -50 mutation likely originated on Hainan Island within 3900 years, subsequently spreading to the mainland and experiencing lineage-specific selection. HbE exhibits substantial haplotype heterogeneity in Yunnan, with network analyses indicating bidirectional disseminations between southern China and South/Southeast Asia. We further suggest an ameliorating effect of HG2, associated with elevated hemoglobin and fetal hemoglobin levels. These findings highlight multi-centric origins of β-thalassemia mutations and underscore the evolutionary context shaping their clinical impact.

β-thalassemia mutations show striking population differences, but their evolutionary origins are unclear. Here, the authors trace multiple independent origins of common β-thalassemia mutations in southern China, shaped by agricultural expansion, migration, and local selection.

## Linked entities

- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** HBB (hemoglobin subunit beta) [NCBI Gene 3043] {aka CD113t-C, ECYT6, beta-globin}, HBE1 (hemoglobin subunit epsilon 1) [NCBI Gene 3046] {aka HBE}
- **Diseases:** beta-thalassemia (MESH:D017086)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12635081/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12635081/full.md

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Source: https://tomesphere.com/paper/PMC12635081