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Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs.
Vossen, Carla Y; van Hylckama Vlieg, Astrid; Teruel-Montoya, Raúl; Salloum-Asfar, Salam; de Haan, Hugoline; Corral, Javier; Reitsma, Pieter; Koeleman, Bobby P C; Martínez, Constantino.
Afiliación
  • Vossen CY; Medical Genetics, University Medical Centre Utrecht, Utrecht, the Netherlands.
  • van Hylckama Vlieg A; Clinical Epidemiology, Leiden University Medical Centre, Leiden, the Netherlands.
  • Teruel-Montoya R; Clinical Epidemiology, Leiden University Medical Centre, Leiden, the Netherlands.
  • Salloum-Asfar S; CIBERER (CB15/00055), Murcia, Spain.
  • de Haan H; Servicio de Hematología y Oncología Médica. Hospital Universitario Morales Meseguer y Centro Regional de Hemodonación, IMIB-Arrixaca, Universidad de Murcia, Murcia, Spain.
  • Corral J; Clinical Epidemiology, Leiden University Medical Centre, Leiden, the Netherlands.
  • Reitsma P; Servicio de Hematología y Oncología Médica. Hospital Universitario Morales Meseguer y Centro Regional de Hemodonación, IMIB-Arrixaca, Universidad de Murcia, Murcia, Spain.
  • Koeleman BPC; Einthoven Laboratory for Experimental Vascular Medicine, Leiden University Medical Centre, Leiden, the Netherlands.
  • Martínez C; Thrombosis and Haemostasis, Leiden University Medical Centre, Leiden, the Netherlands.
Br J Haematol ; 177(5): 782-790, 2017 06.
Article en En | MEDLINE | ID: mdl-28444748
ABSTRACT
MicroRNAs have been recognized as critical regulators of gene expression and might affect the risk of venous thrombosis. We aimed to identify 3' untranslated region (UTR) variants in coagulation genes that influence coagulation factor levels and venous thrombosis risk. The 3'UTR of coagulation genes were sequenced in subjects with extremely high or low plasma levels of these factors in two case-control studies. In total, 28 variants were identified. Five single nucleotide polymorphisms (SNPs) were predominantly present in one extreme level group (F2 rs1799963, F8 rs1050705 and F11 rs4253429, rs4253430 and rs1062547). Additional to F2 rs1799963, F8 rs1050705 (in men) and F11 rs4253430 were associated with an increased risk of venous thrombosis albeit confidence intervals were wide. The three F11 SNPs were in high linkage disequilibrium with functional variants rs2289252 and rs2036914. Rs1062547 and rs4253430 were associated with a significant increase of plasma FXI activity in heterozygotes and homozygotes in wild-type controls. In silico prediction revealed that these SNPs might disturb the binding sites of miR-544 and miR-513a-3p. Only miR-544 provoked a significant decrease of the luciferase activity that was not observed with a rs4253430 mutated vector. In conclusion, these results reinforce that microRNAs are candidates to play a role in haemostasis and complex disorders, such as thrombosis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Coagulación Sanguínea / Trombosis de la Vena / Regiones no Traducidas 3' / MicroARNs Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Br J Haematol Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Factores de Coagulación Sanguínea / Trombosis de la Vena / Regiones no Traducidas 3' / MicroARNs Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male / Middle aged Idioma: En Revista: Br J Haematol Año: 2017 Tipo del documento: Article País de afiliación: Países Bajos