Author
Listed:
- Qianqian Zhang
(Postdoctoral Innovation Practice Base of Southern Medical University, Dongguan Maternal and Child Health Care Hospital
Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Jialong Li
(Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Haoyang Huang
(Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Xuan Shang
(Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Yuhua Ye
(Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Wei Zhang
(Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Peng Lin
(Dongguan Maternal and Children Health Care Hospital, Prenatal Diagnostic Center)
- Yi Gong
(People’s Hospital of Zhengzhou University, Henan Provincial Key Laboratory of Genetic Diseases, Henan Provincial People’s Hospital)
- Boon-Peng Hoh
(IMU University, Division of Applied Biomedical Sciences and Biotechnology, School of Health Sciences)
- Qingming Luo
(Postdoctoral Innovation Practice Base of Southern Medical University, Dongguan Maternal and Child Health Care Hospital
Dongguan Maternal and Children Health Care Hospital, Prenatal Diagnostic Center)
- Tizhen Yan
(Dongguan Maternal and Children Health Care Hospital, Prenatal Diagnostic Center)
- Xinghua Pan
(Postdoctoral Innovation Practice Base of Southern Medical University, Dongguan Maternal and Child Health Care Hospital
Macau University of Science and Technology, Precision Regenerative Medicine Research Centre, Medical Science Division
Southern Medical University, Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences)
- Mark Stoneking
(Max Planck Institute for Evolutionary Anthropology, Department of Evolutionary Genetics
CNRS & Université de Lyon, Biométrie et Biologie Évolutive, UMR 5558)
- Shuhua Xu
(Fudan University, State Key Laboratory of Genetics and Development of Complex Phenotypes, Center for Evolutionary Biology, School of Life Sciences)
- Xiangmin Xu
(Southern Medical University, Department of Medical Genetics, School of Basic Medical Sciences
Southern Medical University, Innovation Center for Diagnostics and Treatment of Thalassemia, Nanfang Hospital)
- Lian Deng
(Fudan University, State Key Laboratory of Genetics and Development of Complex Phenotypes, Center for Evolutionary Biology, School of Life Sciences)
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.
Suggested Citation
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 X, 2025.
"Multi-centric origins and gene flow shape the diversity of β-thalassemia mutations in Southern East Asia,"
Nature Communications, Nature, vol. 16(1), pages 1-14, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-025-65019-0
DOI: 10.1038/s41467-025-65019-0
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