| Literature DB >> 31207231 |
Qiaoli Li1, Vivek M Philip2, Timothy M Stearns2, Jason A Bubier2, Benjamin L King3, Benjamin E Low2, Michael V Wiles2, Amir Hossein Saeidian4, Beth A Sundberg2, Jouni Uitto5, John P Sundberg2.
Abstract
Pseudoxanthoma elasticum, a prototype of heritable multisystem ectopic mineralization disorders, is caused by mutations in the ABCC6 gene encoding a putative efflux transporter, ABCC6. The phenotypic spectrum of pseudoxanthoma elasticum varies, and the correlation between genotype and phenotype has not been established. To identify genetic modifiers, we performed quantitative trait locus analysis in inbred mouse strains that carry the same hypomorphic allele in Abcc6 yet with highly variable ectopic mineralization phenotypes of pseudoxanthoma elasticum. Abcc6 was confirmed as a major determinant for ectopic mineralization in multiple tissues. Integrative analysis using functional genomics tools that included GeneWeaver, String, and Mouse Genome Informatics identified a total of nine additional candidate modifier genes that could influence the organ-specific ectopic mineralization phenotypes. Integration of the candidate genes into the existing ectopic mineralization gene network expands the current knowledge on the complexity of the network that, as a whole, governs ectopic mineralization in soft connective tissues.Entities:
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Year: 2019 PMID: 31207231 PMCID: PMC6874750 DOI: 10.1016/j.jid.2019.04.023
Source DB: PubMed Journal: J Invest Dermatol ISSN: 0022-202X Impact factor: 8.551