Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: Genotypic overlap with pseudoxanthoma elasticum

Qiaoli Li, Jill L. Brodsky, Laura K. Conlin, Bruce Pawel, Andrew C. Glatz, Rachel I. Gafni, Leon Schurgers, Jouni Uitto, Hakon Hakonarson, Matthew A. Deardorff, Michael A. Levine

Research output: Contribution to journalArticle

Abstract

Generalized arterial calcification of infancy (GACI) is an autosomal recessive disorder characterized by congenital calcification of large- and medium-sized arteries, associated with early myocardial infarction, heart failure, and stroke, and premature death. Most cases of GACI are caused by mutations in the ENPP1 gene. We first studied two siblings with GACI from a non-consanguineous family without mutations in the ENPP1 gene. To search for disease-causing mutations, we identified genomic regions shared between the two affected siblings but not their unaffected parents or brother. The ABCC6 gene, which is mutated in pseudoxanthoma elasticum (PXE), resided within a small region of homozygosity shared by the affected siblings. Sequence analysis of ABCC6 revealed that the two affected siblings were homozygous for the missense mutation p.R1314W. Subsequently, ABCC6 mutations were identified in five additional GACI families with normal ENPP1 sequences. Genetic mutations in ABCC6 in patients with PXE are associated with ectopic tissue mineralization in the skin and arterial blood vessels. Thus, our findings provide additional evidence that the ABCC6 gene product inhibits calcification under physiologic conditions and confirm a second locus for GACI. In addition, our study emphasizes the potential utility of shared homozygosity mapping to identify genetic causes of inherited disorders.

Original languageEnglish (US)
Pages (from-to)658-665
Number of pages8
JournalJournal of Investigative Dermatology
Volume134
Issue number3
DOIs
StatePublished - Mar 2014
Externally publishedYes

Fingerprint

Pseudoxanthoma Elasticum
Rubber
Siblings
Genes
Mutation
Blood vessels
Choristoma
Physiologic Calcification
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Premature Mortality
Missense Mutation
Skin
Sequence Analysis
Blood Vessels
Tissue
Heart Failure
Arteries
Parents
Stroke
Myocardial Infarction

ASJC Scopus subject areas

  • Dermatology
  • Biochemistry
  • Cell Biology
  • Molecular Biology

Cite this

Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy : Genotypic overlap with pseudoxanthoma elasticum. / Li, Qiaoli; Brodsky, Jill L.; Conlin, Laura K.; Pawel, Bruce; Glatz, Andrew C.; Gafni, Rachel I.; Schurgers, Leon; Uitto, Jouni; Hakonarson, Hakon; Deardorff, Matthew A.; Levine, Michael A.

In: Journal of Investigative Dermatology, Vol. 134, No. 3, 03.2014, p. 658-665.

Research output: Contribution to journalArticle

Li, Q, Brodsky, JL, Conlin, LK, Pawel, B, Glatz, AC, Gafni, RI, Schurgers, L, Uitto, J, Hakonarson, H, Deardorff, MA & Levine, MA 2014, 'Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy: Genotypic overlap with pseudoxanthoma elasticum', Journal of Investigative Dermatology, vol. 134, no. 3, pp. 658-665. https://doi.org/10.1038/jid.2013.370
Li, Qiaoli ; Brodsky, Jill L. ; Conlin, Laura K. ; Pawel, Bruce ; Glatz, Andrew C. ; Gafni, Rachel I. ; Schurgers, Leon ; Uitto, Jouni ; Hakonarson, Hakon ; Deardorff, Matthew A. ; Levine, Michael A. / Mutations in the ABCC6 gene as a cause of generalized arterial calcification of infancy : Genotypic overlap with pseudoxanthoma elasticum. In: Journal of Investigative Dermatology. 2014 ; Vol. 134, No. 3. pp. 658-665.
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