Literature DB >> 25305692

14-3-3 tau (YWHAQ) gene promoter hypermethylation in human placenta of preeclampsia.

H Liu1, Y Tang1, X Liu2, Q Zhou2, X Xiao2, F Lan3, X Li4, R Hu2, Y Xiong2, T Peng2.   

Abstract

INTRODUCTION: Disruption of the 14-3-3 tau (YWHAQ) gene has been shown to be involved in preeclampsia (PE). The YWHAQ promoter could be differentially regulated by methylation in severe PE patients.
METHODS: Placental genomic DNA from patients with severe PE (n = 21) and controls who experienced a normal pregnancy (n = 16) was analyzed using dot-blot and immunohistochemistry. The placental methylation patterns of YWHAQ, expression of 14-3-3 tau and ten-eleven translocation (TET), were confirmed by bisulfite sequencing, immunohistochemistry, western blot and real-time PCR, respectively.
RESULTS: Genomic 5 hmC (P < 0.001), expression of 14-3-3 tau (P < 0.01) and TET (P < 0.05) were down-regulated, whereas 5 mC was up-regulated (P < 0.001) in preeclamptic placentas. Significant hypermethylation of the YWHAQ promoter was detected in PE placentas compared with control samples (19.1% vs. 9.4%, P = 0.0095). PE-specific hypermethylation of CpG2 - 4, CpG9, CpG17, CpG19 was identified in PE patients compared with controls (CpG2: 13.3% vs. 2.5%, P < 0.0001; CpG3: 14.8% vs. 3.1%, P < 0.0001; CpG4: 19.5% vs. 5.0%, P < 0.0001; CpG9: 15.7% vs. 5.0%, P = 0.0018; CpG17: 16.2% vs. 6.3%, P = 0.0003; and CpG19: 78.1% vs. 59.4%, P < 0.0001). DISCUSSION: The observed participation of 14-3-3 tau in the regulation of the placental epigenome may participate in the molecular mechanisms that govern the pathological process of PE, although this requires further evaluation.
Copyright © 2014 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  14-3-3 tau; 5 hmC; Methylation; Placenta; Preeclampsia; TETs

Mesh:

Substances:

Year:  2014        PMID: 25305692     DOI: 10.1016/j.placenta.2014.09.016

Source DB:  PubMed          Journal:  Placenta        ISSN: 0143-4004            Impact factor:   3.481


  12 in total

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8.  MicroRNA-210 Mediates Hypoxia-Induced Repression of Spontaneous Transient Outward Currents in Sheep Uterine Arteries During Gestation.

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9.  Hypoxia-induced TET1 facilitates trophoblast cell migration and invasion through HIF1α signaling pathway.

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