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Structural variants involved in high-altitude adaptation detected using single-molecule long-read sequencing

Author

Listed:
  • Jinlong Shi

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital
    Chinese PLA General Hospital
    Chinese PLA General Hospital)

  • Zhilong Jia

    (Chinese PLA General Hospital
    Chinese PLA General Hospital
    Medical Innovation Research Division of Chinese PLA General Hospital)

  • Jinxiu Sun

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital)

  • Xiaoreng Wang

    (Medical Innovation Research Division of Chinese PLA General Hospital
    State Key Laboratory of Experimental Hematology)

  • Xiaojing Zhao

    (Chinese PLA General Hospital
    Medical Innovation Research Division of Chinese PLA General Hospital)

  • Chenghui Zhao

    (Chinese PLA General Hospital
    Medical Innovation Research Division of Chinese PLA General Hospital)

  • Fan Liang

    (NextOmics Biosciences Inc)

  • Xinyu Song

    (Chinese PLA General Hospital
    Medical Innovation Research Division of Chinese PLA General Hospital)

  • Jiawei Guan

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital)

  • Xue Jia

    (Medical Innovation Research Division of Chinese PLA General Hospital)

  • Jing Yang

    (Medical Innovation Research Division of Chinese PLA General Hospital)

  • Qi Chen

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital)

  • Kang Yu

    (Chinese PLA General Hospital)

  • Qian Jia

    (Chinese PLA General Hospital)

  • Jing Wu

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital)

  • Depeng Wang

    (NextOmics Biosciences Inc)

  • Yuhui Xiao

    (NextOmics Biosciences Inc)

  • Xiaoman Xu

    (NextOmics Biosciences Inc)

  • Yinzhe Liu

    (NextOmics Biosciences Inc)

  • Shijing Wu

    (Chinese PLA General Hospital)

  • Qin Zhong

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital)

  • Jue Wu

    (Chinese PLA General Hospital)

  • Saijia Cui

    (Chinese PLA General Hospital)

  • Xiaochen Bo

    (Beijing Institute of Radiation Medicine)

  • Zhenzhou Wu

    (BioMind Inc)

  • Minsung Park

    (NextOmics Biosciences Inc)

  • Manolis Kellis

    (Broad Institute of MIT and Harvard)

  • Kunlun He

    (Medical Innovation Research Division of Chinese PLA General Hospital
    Chinese PLA General Hospital
    Chinese PLA General Hospital
    Chinese PLA General Hospital)

Abstract

Structural variants (SVs), accounting for a larger fraction of the genome than SNPs/InDels, are an important pool of genetic variation, enabling environmental adaptations. Here, we perform long-read sequencing data of 320 Tibetan and Han samples and show that SVs are highly involved in high-altitude adaptation. We expand the landscape of global SVs, apply robust models of selection and population differentiation combining SVs, SNPs and InDels, and use epigenomic analyses to predict enhancers, target genes and biological functions. We reveal diverse Tibetan-specific SVs affecting the regulatory circuitry of biological functions, including the hypoxia response, energy metabolism and pulmonary function. We find a Tibetan-specific deletion disrupts a super-enhancer and downregulates EPAS1 using enhancer reporter, cellular knock-out and DNA pull-down assays. Our study expands the global SV landscape, reveals the role of gene-regulatory circuitry rewiring in human adaptation, and illustrates the diverse functional roles of SVs in human biology.

Suggested Citation

  • Jinlong Shi & Zhilong Jia & Jinxiu Sun & Xiaoreng Wang & Xiaojing Zhao & Chenghui Zhao & Fan Liang & Xinyu Song & Jiawei Guan & Xue Jia & Jing Yang & Qi Chen & Kang Yu & Qian Jia & Jing Wu & Depeng Wa, 2023. "Structural variants involved in high-altitude adaptation detected using single-molecule long-read sequencing," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-44034-z
    DOI: 10.1038/s41467-023-44034-z
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