Improving the diagnosis of cobalamin and related defects by genomic analysis, plus functional and structural assessment of novel variants
AuthorBrasil, Sandra; Leal, Fátima; Vega, Ana; Navarrete, Rosa; Ecay, María Jesús; Ruiz Desviat, Lourdes; Riera, Casandra; Padilla, Natàlia; De La Cruz, Xavier; Couce, Mari Luz; Martin-Hernández, Elena; Morais, Ana; Pedrón, Consuelo; Peña-Quintana, Luis; Rigoldi, Miriam; Specola, Norma; De Almeida, Isabel Tavares; Vives, Inmaculada; Yahyaoui, Raquel; Rodríguez Pombo, Pilar; Ugarte, Magdalena; Pérez-Cerda, Celia; Merinero, Begoña; Pérez, Belén
EntityUAM. Departamento de Biología Molecular; Centro de Biología Molecular Severo Ochoa (CBM); Instituto de Investigación Sanitaria Hospital Universitario de La Paz (IdiPAZ)
PublisherBMC (part of Springer Nature)
10.1186/s13023-018-0862-yOrphanet Journal of Rare Diseases 13 (2018): 125
Funded byThis work was funded by grants PI13/01239-PI16/00573; Fundación Isabel Gemio-Fundación La Caixa (LCF/PR/PR16/11110018).
ProjectGobierno de España. PI13/01239-; Gobierno de España. PI16/00573
SubjectsCobalamin disorders; Homocystinuria; Massive parallel sequencing; Methylmalonic aciduria; Biología y Biomedicina / Biología
Rights© 2018 The Author(s).
Esta obra está bajo una Licencia Creative Commons Atribución 4.0 Internacional.
Background: Cellular cobalamin defects are a locus and allelic heterogeneous disorder. The gold standard for coming to genetic diagnoses of cobalamin defects has for some time been gene-by-gene Sanger sequencing of individual DNA fragments. Enzymatic and cellular methods are employed before such sequencing to help in the selection of the gene defects to be sought, but this is time-consuming and laborious. Furthermore some cases remain undiagnosed because no biochemical methods have been available to test for cobalamin absorption and transport defects. Results: This paper reports the use of massive parallel sequencing of DNA (exome analysis) for the accurate and rapid genetic diagnosis of cobalamin-related defects in a cohort of affected patients. The method was first validated in an initial cohort with different cobalamin defects. Mendelian segregation, the frequency of mutations, and the comprehensive structural and functional analysis of gene variants, identified disease-causing mutations in 12 genes involved in the absorption and synthesis of active cofactors of vitamin B 12 (22 cases), and in the non-cobalamin metabolism-related genes ACSF3 (in four biochemically misdiagnosed patients) and SUCLA2 (in one patient with an unusual presentation). We have identified thirteen new variants all classified as pathogenic according to the ACGM recommendation but four were classified as variant likely pathogenic in MUT and SUCLA2. Functional and structural analysis provided evidences to classify them as pathogenic variants. Conclusions: The present findings suggest that the technology used is sufficiently sensitive and specific, and the results it provides sufficiently reproducible, to recommend its use as a second-tier test after the biochemical detection of cobalamin disorder markers in the first days of life. However, for accurate diagnoses to be made, biochemical and functional tests that allow comprehensive clinical phenotyping are also needed.
Google Scholar:Brasil, Sandra - Leal, Fátima - Vega, Ana - Navarrete, Rosa - Ecay, María Jesús - Ruiz Desviat, Lourdes - Riera, Casandra - Padilla, Natàlia - De La Cruz, Xavier - Couce, Mari Luz - Martin-Hernández, Elena - Morais, Ana - Pedrón, Consuelo - Peña-Quintana, Luis - Rigoldi, Miriam - Specola, Norma - De Almeida, Isabel Tavares - Vives, Inmaculada - Yahyaoui, Raquel - Rodríguez Pombo, Pilar - Ugarte, Magdalena - Pérez-Cerda, Celia - Merinero, Begoña - Pérez, Belén
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