Journal Article

Coinheritance of COL4A5 and MYO1E mutations accentuate the severity of kidney disease

Webb, Nicholas J. A., Bierzynska, Agnieszka, Campbell, Joanna, Welsh, Gavin I., Randles, Michael J., Kerr, Bronwyn, Batra, Gauri, Hillman, Katherine A., Woolf, Adrian S., Storey, Helen, Saleem, Moin A., Lennon, Rachel, Stuart, Helen M., Koziell, Ania, Flinter, Frances A.

2015

Overview

Background Mutations in podocyte and basement membrane genes are associated with a growing spectrum of glomerular disease affecting adults and children. Investigation of familial cases has helped to build understanding of both normal physiology and disease. Methods We investigated a consanguineous family with a wide clinical phenotype of glomerular disease using clinical, histological, and new genetic studies. Results We report striking variability in severity of nephropathy within an X-linked Alport syndrome (XLAS) family. Four siblings each carried a mutant COL4A5 allele, p.(Gly953Val) and p.(Gly1033Arg). Two boys had signs limited to hematuria and mild/moderate proteinuria. In striking contrast, a sister presented with end-stage renal disease (ESRD) at 8 years of age and an infant brother presented with nephrotic syndrome, progressing to ESRD by 3 years of age. Both were subsequently found to have homozygous variants in MYO1E , p.(Lys118Glu) and p.(Thr876Arg). MYO1E is a gene implicated in focal segmental glomerulosclerosis and it encodes a podocyte-expressed non-muscle myosin. Bioinformatic modeling demonstrated that the collagen IV-alpha3,4,5 extracellular network connected via known protein–protein interactions to intracellular myosin 1E. Conclusions COL4A5 and MYO1E mutations may summate to perturb common signaling pathways, resulting in more severe disease than anticipated independently. We suggest screening for MYO1E and other non- COL4 ‘podocyte gene’ mutations in XLAS when clinical nephropathy is more severe than expected for an individual’s age and sex.

• Publisher: Springer Berlin Heidelberg,Springer,Springer Nature B.V
• Subject: Adult / Child / Child, Preschool / Collagen / Collagen Type IV - genetics / Female / Gene mutation / Genes / Genetics / Health aspects / Humans / Infant / Inheritance Patterns - genetics / Kidney diseases / Kidney Glomerulus - pathology / Male / Medicine / Medicine & Public Health / Mutation / Myosin Type I - genetics / Nephritis, Hereditary - diagnosis / Nephritis, Hereditary - genetics / Nephritis, Hereditary - physiopathology / Nephrology / Original / Original Article / Pediatrics / Pedigree / Proteins / Release dates / Severity of Illness Index / Siblings / Teenage boys / Transmission electron microscopes / Transmission electron microscopy / Urology