Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.

Antithrombin is a crucial anticoagulant serpin whose even moderate deficiency significantly increases the risk of thrombosis. Most cases with antithrombin deficiency carried genetic defects affecting exons or flanking regions of SERPINC1.We aimed to identify regulatory mutations inSERPINC1 through s...

Full description

Bibliographic Details
Main Authors: Mara Toderici, María Eugenia de la Morena-Barrio, José Padilla, Antonia Miñano, Ana Isabel Antón, Juan Antonio Iniesta, María Teresa Herranz, Nuria Fernández, Vicente Vicente, Javier Corral
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2016-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4803246?pdf=render
id doaj-7a35cb8e0c764a80913f4c7162ecced7
record_format Article
spelling doaj-7a35cb8e0c764a80913f4c7162ecced72020-11-25T01:22:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032016-01-01113e015215910.1371/journal.pone.0152159Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.Mara TodericiMaría Eugenia de la Morena-BarrioJosé PadillaAntonia MiñanoAna Isabel AntónJuan Antonio IniestaMaría Teresa HerranzNuria FernándezVicente VicenteJavier CorralAntithrombin is a crucial anticoagulant serpin whose even moderate deficiency significantly increases the risk of thrombosis. Most cases with antithrombin deficiency carried genetic defects affecting exons or flanking regions of SERPINC1.We aimed to identify regulatory mutations inSERPINC1 through sequencing the promoter, intron 1 and 2 of this gene in 23 patients with antithrombin deficiency but without known genetic defects. Three cases with moderate antithrombin deficiency (63-78%) carried potential regulatory mutations. One located 200 bp before the initiation ATG and two in intron 1. These mutations disrupted two out of five potential vitamin D receptor elements (VDRE) identified in SERPINC1 with different software. One genetic defect, c.42-1060_-1057dupTTGA, was a new low prevalent polymorphism (MAF: 0.01) with functional consequences on plasma antithrombin levels. The relevance of the vitamin D pathway on the regulation of SERPINC1 was confirmed in a cell model. Incubation of HepG2 with paricalcitol, a vitamin D analog, increased dose-dependently the levels of SERPINC1transcripts and antithrombin released to the conditioned medium. This study shows further evidence of the transcriptional regulation of SERPINC1 by vitamin D and first describes the functional and pathological relevance of mutations affecting VDRE of this gene. Our study opens new perspectives in the search of new genetic defects involved in antithrombin deficiency and the risk of thrombosis as well as in the design of new antithrombotic treatments.http://europepmc.org/articles/PMC4803246?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Mara Toderici
María Eugenia de la Morena-Barrio
José Padilla
Antonia Miñano
Ana Isabel Antón
Juan Antonio Iniesta
María Teresa Herranz
Nuria Fernández
Vicente Vicente
Javier Corral
spellingShingle Mara Toderici
María Eugenia de la Morena-Barrio
José Padilla
Antonia Miñano
Ana Isabel Antón
Juan Antonio Iniesta
María Teresa Herranz
Nuria Fernández
Vicente Vicente
Javier Corral
Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
PLoS ONE
author_facet Mara Toderici
María Eugenia de la Morena-Barrio
José Padilla
Antonia Miñano
Ana Isabel Antón
Juan Antonio Iniesta
María Teresa Herranz
Nuria Fernández
Vicente Vicente
Javier Corral
author_sort Mara Toderici
title Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
title_short Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
title_full Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
title_fullStr Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
title_full_unstemmed Identification of Regulatory Mutations in SERPINC1 Affecting Vitamin D Response Elements Associated with Antithrombin Deficiency.
title_sort identification of regulatory mutations in serpinc1 affecting vitamin d response elements associated with antithrombin deficiency.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2016-01-01
description Antithrombin is a crucial anticoagulant serpin whose even moderate deficiency significantly increases the risk of thrombosis. Most cases with antithrombin deficiency carried genetic defects affecting exons or flanking regions of SERPINC1.We aimed to identify regulatory mutations inSERPINC1 through sequencing the promoter, intron 1 and 2 of this gene in 23 patients with antithrombin deficiency but without known genetic defects. Three cases with moderate antithrombin deficiency (63-78%) carried potential regulatory mutations. One located 200 bp before the initiation ATG and two in intron 1. These mutations disrupted two out of five potential vitamin D receptor elements (VDRE) identified in SERPINC1 with different software. One genetic defect, c.42-1060_-1057dupTTGA, was a new low prevalent polymorphism (MAF: 0.01) with functional consequences on plasma antithrombin levels. The relevance of the vitamin D pathway on the regulation of SERPINC1 was confirmed in a cell model. Incubation of HepG2 with paricalcitol, a vitamin D analog, increased dose-dependently the levels of SERPINC1transcripts and antithrombin released to the conditioned medium. This study shows further evidence of the transcriptional regulation of SERPINC1 by vitamin D and first describes the functional and pathological relevance of mutations affecting VDRE of this gene. Our study opens new perspectives in the search of new genetic defects involved in antithrombin deficiency and the risk of thrombosis as well as in the design of new antithrombotic treatments.
url http://europepmc.org/articles/PMC4803246?pdf=render
work_keys_str_mv AT maratoderici identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT mariaeugeniadelamorenabarrio identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT josepadilla identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT antoniaminano identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT anaisabelanton identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT juanantonioiniesta identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT mariateresaherranz identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT nuriafernandez identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT vicentevicente identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
AT javiercorral identificationofregulatorymutationsinserpinc1affectingvitamindresponseelementsassociatedwithantithrombindeficiency
_version_ 1725127699725287424