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Non-collagen genes role in digenic Alport syndrome.
Daga, S; Fallerini, C; Furini, S; Pecoraro, C; Scolari, F; Ariani, F; Bruttini, M; Mencarelli, M A; Mari, F; Renieri, A; Pinto, A M.
Afiliación
  • Daga S; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Viale Bracci, 2, 53100, Siena, Italy.
  • Fallerini C; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Viale Bracci, 2, 53100, Siena, Italy.
  • Furini S; Department of Medical Biotechnologies, University of Siena, Siena, Italy.
  • Pecoraro C; Pediatric Nephrology Unit, Santobono-Pausilipon Hospital, Naples, Italy.
  • Scolari F; Department of Nephrology, University of Brescia, Brescia, Italy.
  • Ariani F; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Viale Bracci, 2, 53100, Siena, Italy.
  • Bruttini M; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Mencarelli MA; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Viale Bracci, 2, 53100, Siena, Italy.
  • Mari F; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Renieri A; Genetica Medica, Azienda Ospedaliera Universitaria Senese, Siena, Italy.
  • Pinto AM; Medical Genetics Unit, University of Siena, Policlinico Le Scotte, Viale Bracci, 2, 53100, Siena, Italy.
BMC Nephrol ; 20(1): 70, 2019 02 26.
Article en En | MEDLINE | ID: mdl-30808327
BACKGROUND: Alport syndrome is a clinically heterogeneous nephropathy characterized by severe symptomatology at kidney level due to ultrastructural lesions of the glomerular basement membrane (GBM) as consequence of mutations in COL4 genes. The disease has been linked to COL4A3/COL4A4/COL4A5 mutations, which impair GBM functionality and can be inherited in a dominant, recessive or X-linked transmission. Although a targeted Next Generation Sequencing approach has allowed identifying families with pathogenic mutations in more than one COL4 α3-α4-α5 heterotrimer encoding genes, leading to conclude for a digenic pattern of inheritance, the role of non-collagen genes in digenic Alport syndrome has not yet been established. METHODS: We employed a whole-exome sequencing approach on three families in whom a digenic pattern of transmission could be suspected because of a likely biparental contribution or an unexplained phenotype in the proband. RESULTS: We identified in the three probands hypomorphic LAMA5 mutations co-inherited with pathogenic COL4 α4-α5 chains mutations. Segregation analysis revealed that the combination of LAMA5/COL4 variants co-segregate with a fully penetrant phenotype in line with a digenic inheritance. In one of the three probands an hypomorphic variant in NPHS2 was also found, suggesting that role of other kidney disease related-genes as modifiers. CONCLUSION: These findings validate the impact of LAMA5 mutations in digenic ATS and highlight the role of extracellular matrix's genes, basement membrane, slit diaphragm and podocyte cytoskeleton in ATS. This underline the need for a more extensive panel approach in the presence of a digenic ATS, in order to better define clinical severity and recurrence risk for family members.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Laminina / Colágeno Tipo IV / Péptidos y Proteínas de Señalización Intracelular / Proteínas de la Membrana / Nefritis Hereditaria Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: BMC Nephrol Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Laminina / Colágeno Tipo IV / Péptidos y Proteínas de Señalización Intracelular / Proteínas de la Membrana / Nefritis Hereditaria Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Revista: BMC Nephrol Asunto de la revista: NEFROLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Italia Pais de publicación: Reino Unido