Denaturing HPLC profiling of the ABCA4 gene for reliable detection of allelic variations

Stefania Stenirri, Isabella Fermo, Stefania Battistella, Silvia Galbiati, Nadia Soriani, Rita Paroni, Maria Pia Manitto, Elisabetta Martina, Rosario Brancato, Rando Allikmets, Maurizio Ferrari, Laura Cremonesi

Research output: Contribution to journalArticlepeer-review


Background: Mutations in the retina-specific ABC transporter (ABCA4) gene have been associated with several forms of macular degenerations. Because the high complexity of the molecular genotype makes scanning of the ABCA4 gene cumbersome, we describe here the first use of denaturing HPLC (DHPLC) to screen for ABCA4 mutations. Methods: Temperature conditions were designed for all 50 exons based on effective separation of 83 samples carrying 86 sequence variations and 19 mutagenized controls. For validation, samples from 23 previously characterized Stargardt patients were subjected to DH-PLC profiling. Subsequently, samples from a cohort of 30 patients affected by various forms of macular degeneration were subjected to DHPLC scanning under the same conditions. Results: DHPLC profiling not only identified all 132 sequence alterations previously detected by double-gradient denaturing gradient gel electrophoresis but also identified 5 sequence alterations that this approach had missed. Moreover, DHPLC scanning of an additional panel of 30 previously untested patients led to the identification of 26 different mutations and 29 polymorphisms, accounting for 203 sequence variations on 29 of the 30 patients screened. In total, the DHPLC approach allowed us to identify 16 mutations that had never been reported before. Conclusions: These results provide strong support for the use of DHPLC for molecular characterization of the ABCA4 gene.

Original languageEnglish
Pages (from-to)1336-1343
Number of pages8
JournalClinical Chemistry
Issue number8
Publication statusPublished - Aug 2004

ASJC Scopus subject areas

  • Clinical Biochemistry


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