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Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes | BMC Medical Genomics | Full Text

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes | BMC Medical Genomics | Full Text
Biomed Central
BMC Medical Genomics

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

  • John K. L. Wong,
  • Desmond Campbell,
  • Ngoc Diem Ngo,
  • Fanny Yeung,
  • Guo Cheng,
  • Clara S. M. Tang,
  • Patrick H. Y. Chung,
  • Ngoc Son Tran,
  • Man-ting So,
  • Stacey S. Cherny,
  • Pak C. Sham,
  • Paul K. Tam and
  • Maria-Mercè Garcia-BarceloEmail author
BMC Medical GenomicsBMC series – open, inclusive and trusted20169:75
DOI: 10.1186/s12920-016-0236-z
Received: 13 September 2016
Accepted: 7 December 2016
Published: 12 December 2016

Abstract

Background

Congenital dilatation of the bile-duct (CDD) is a rare, mostly sporadic, disorder that results in bile retention with severe associated complications. CDD affects mainly Asians. To our knowledge, no genetic study has ever been conducted.

Methods

We aim to identify genetic risk factors by a “trio-based” exome-sequencing approach, whereby 31 CDD probands and their unaffected parents were exome-sequenced. Seven-hundred controls from the local population were used to detect gene-sets significantly enriched with rare variants in CDD patients.

Results

Twenty-one predicted damaging de novo variants (DNVs; 4 protein truncating and 17 missense) were identified in several evolutionarily constrained genes (p < 0.01). Six genes carrying DNVs were associated with human developmental disorders involving epithelial, connective or bone morphologies (PXDN, RTEL1, ANKRD11, MAP2K1, CYLD, ACAN) and four linked with cholangio- and hepatocellular carcinomas (PIK3CA, TLN1 CYLD, MAP2K1). Importantly, CDD patients have an excess of DNVs in cancer-related genes (p < 0.025). Thirteen genes were recurrently mutated at different sites, forming compound heterozygotes or functionally related complexes within patients.

Conclusions

Our data supports a strong genetic basis for CDD and show that CDD is not only genetically heterogeneous but also non-monogenic, requiring mutations in more than one genes for the disease to develop. The data is consistent with the rarity and sporadic presentation of CDD.

Keywords

Choledochal cyst Exome De novo Rare variants association

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