Molecular modeling indicates distinct classes of missense variants with mild and severe XLRS phenotypes

Yuri V. Sergeev, Susan Vitale, Paul A. Sieving, Ajoy Vincent, Anthony G. Robson, Anthony T. Moore, Andrew R. Webster, Graham E. Holder

Research output: Contribution to journalArticlepeer-review

Abstract

X-linked retinoschisis (XLRS) is a vitreo-retinal degeneration caused by mutations in the RS1 gene which encodes the protein retinoschisin (RS1), required for the structural and functional integrity of the retina. Data are presented from a group of 38 XLRS patients from Moorfields Eye Hospital (London, UK) who had one of 18 missense mutations in RS1. Patients were grouped based on mutation severity predicted by molecular modeling: mild (class I), moderate (intermediate) and severe (class II). Most patients had an electronegative scotopic bright flash electroretinogram (ERG) (reduced b/a-wave ratio) in keeping with predominant inner retinal dysfunction. An association between the type of structural RS1 alterations and the severity of b/a-wave reduction was found in all but the oldest group of patients, significant in patients aged 15-30 years. Severe RS1 missense changes were associated with a lower ERG b/a ratio than were mild changes, suggesting that the extent of inner retinal dysfunction is influenced by the effect of the mutations on protein structure. The majority of class Imutationsshowednochanges involving cysteine residues. Class IImutationscausedsevere perturbationsdueto the removal or insertion of cysteine residues or due to changes in the hydrophobic core. The ERG b/a ratio in intermediate cases was abnormal but showed significant variability, possibly related to the role of proline or arginine residues. We also conducted a second study, using a completely independent cohort, to indicate a genotype- ERG phenotype correlation.

Original languageEnglish (US)
Article numberddt329
Pages (from-to)4756-4767
Number of pages12
JournalHuman molecular genetics
Volume22
Issue number23
DOIs
StatePublished - Dec 2013
Externally publishedYes

ASJC Scopus subject areas

  • Molecular Biology
  • Genetics
  • Genetics(clinical)

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