{
  "abstract": "Background Primary cilia are essential for skeletal development by coordinating key signalling pathways in osteoblasts and chondrocytes. While pathogenic variants in approximately 40 genes have been linked to skeletal ciliopathies, additional causative genes remain to be identified. Although DNAH10 is well characterised in motile cilia, its role in primary cilia remains unclear.Methods Whole-exome sequencing was performed in two individuals with skeletal developmental abnormalities and identified biallelic DNAH10 variants. In vitro assays were used to assess the effects of these variants on DNAH10 protein abundance. Dnah10 knockout mice were generated to investigate the associated skeletal phenotypes and underlying mechanisms.Results Biallelic DNAH10 variants were identified in two individuals with skeletal developmental abnormalities. In vitro, these missense variants were associated with reduced DNAH10 protein abundance. Dnah10-deficient mice recapitulated key skeletal features, including polydactyly, impaired cartilage development and abnormal ossification. Mechanistically, Dnah10 loss was associated with abnormal primary cilia morphology, attenuated Hedgehog signalling, impaired osteoblast differentiation and defective chondrocyte maturation.Conclusion Our findings support DNAH10 as a candidate gene associated with skeletal developmental abnormalities and ciliary dysfunction and suggest a previously underappreciated role for DNAH10 in primary cilia-related skeletal development beyond its established role in motile cilia.",
  "authors": [
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Rui Zheng"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Xinrong Du"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Jierui Yan"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Gelin Huang"
    },
    {
      "affiliations": [
        "Children’s Hospital of Fudan University, Shanghai, China"
      ],
      "name": "Zhuoyao Guo"
    },
    {
      "affiliations": [
        "Cardiothoracic Surgery Department, Children’s Hospital of Fudan University, Shanghai, China"
      ],
      "name": "Wei Li"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Hanyun Que"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Yuting Wen"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Fei Yan"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Daijuan Chen"
    },
    {
      "affiliations": [
        "National Center for Birth Defects Monitoring, West China Second Hospital of Sichuan University, Dazhou, Sichuan, China"
      ],
      "name": "Li Dai"
    },
    {
      "affiliations": [
        "State Key Laboratory of Oral Diseases, Sichuan University, Chengdu, China"
      ],
      "name": "Yu Shi"
    },
    {
      "affiliations": [
        "Cardiothoracic Surgery Department, Children’s Hospital of Fudan University, Shanghai, China"
      ],
      "name": "Weicheng Chen"
    },
    {
      "affiliations": [
        "Joint Laboratory of Reproductive Medicine, SCU-CUHK, Key Laboratory of Obstetric, Gynaecologic and Paediatric Diseases and Birth Defects of Ministry of Education, West China Second University Hospital, Sichuan University, Chengdu, Sichuan, China"
      ],
      "name": "Wenming Xu"
    }
  ],
  "title": "Biallelic variants in DNAH10 are associated with skeletal developmental abnormalities and ciliary dysfunction",
  "uid": "d3bb14d8-0eed-50e7-bf9d-7f549379cbf9"
}