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Expressional and epigenetic alterations of placental serine protease inhibitors: SERPINA3 is a potential marker of preeclampsia

Authors :
V. Tsatsaris
Virginie Rigourd
Florence Busato
Ivo Gut
Bruno Carbonne
Françoise Ferré
Paul Laissue
Sonia T. Chelbi
François Goffinet
Françoise Mondon
R. Rebourcet
Thérèse-Marie Mignot
Christophe Buffat
Daniel Vaiman
Jörg Tost
Hélène Jammes
Institut Cochin (UMR_S567 / UMR 8104)
Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)
Biologie du développement et reproduction (BDR)
Centre National de la Recherche Scientifique (CNRS)-École nationale vétérinaire d'Alfort (ENVA)-Institut National de la Recherche Agronomique (INRA)
Assistance Publique - Hôpitaux de Marseille (APHM)
Centre National de Génotypage (CNG)
Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)
Unité de recherche Génétique Biochimique et Cytogénétique (LGBC)
Institut National de la Recherche Agronomique (INRA)
Source :
Hypertension, Hypertension, American Heart Association, 2007, 49 (1), pp.76-83
Publication Year :
2006

Abstract

Preeclampsia is the major pregnancy-induced hypertensive disorder. It modifies the expression profile of placental genes, including several serine protease inhibitors ( SERPINs ). The objective of this study was to perform a systematic expression analysis of these genes in normal and pathological placentas and to pinpoint epigenetic alterations inside their promoter regions. Expression of 18 placental SERPINs was analyzed by quantitative RT-PCR on placentas from pregnancies complicated by preeclampsia, intrauterine growth restriction, or both and was compared with normal controls. SERPINA3, A5, A8, B2, B5 , and B7 presented significant differences in expression in ≥1 pathological situation. In parallel, the methylation status of the CpG islands located in their promoter regions was studied on a sample of control and preeclamptic placentas. Ten SERPIN promoters were either totally methylated or totally unmethylated, whereas SERPINA3, A5 , and A8 presented complex methylation profiles. For SERPINA3 , the analysis was extended to 81 samples and performed by pyrosequencing. For the SERPINA3 CpG island, the average methylation level was significantly diminished in preeclampsia and growth restriction. The hypomethylated CpGs were situated at putative binding sites for developmental and stress response (hypoxia and inflammation) factors. Our results provide one of the first observations of a specific epigenetic alteration in human placental diseases and provide new potential markers for an early diagnosis.

Details

ISSN :
15244563 and 0194911X
Volume :
49
Issue :
1
Database :
OpenAIRE
Journal :
Hypertension (Dallas, Tex. : 1979)
Accession number :
edsair.doi.dedup.....7d8c4ded0d46a3e91dcc5acbe496bd14