Literature DB >> 33555507

Genome wide methylation analysis to uncover genes related to recurrent pregnancy loss.

Lixia Zhou1, Yudong Pu1, Yuxun Zhou2, Bin Wang2, Ye Chen3, Yang Bai3, Shuzhen He4.   

Abstract

BACKGROUND: Recurrent pregnancy loss (RPL) refers to two or more consecutive spontaneous abortion before 24 weeks of gestation, representing 1% of couples of childbearing age. Epigenetic factors including dysregulation of DNA methylation of some genes may play a role in RPL.
OBJECTIVE: To identify RPL related genes modulated by DNA methylation expressed in decidua and blood.
METHODS: Three decidua samples each from RPL patients and normal controls were recruited to perform genome-wide bisulfite sequencing (GWBS) and transcriptome sequencing. Based on the above results, 22.52 kb of differential methylation regions (DMRs) from 17 genes were verified by bisulfite sequencing PCR at specific region (Hi-MethylSeq) in another 15 decidua (7RPL vs. 8 Controls) and 13 blood (5RPL vs. 8 Controls) samples.
RESULTS: 23 genes showed significantly differential cytosine methylation status and distinct expression level between PRL patients and healthy controls synergistically. Three signaling pathways were found to be shared between genes with both hypomethylated differential methylation regions (DMR) and upregulated differential gene expression (DGE). The results from Hi-MethylSeq showed that the hypermethylation of SGK1 in both blood and decidua samples in RPL patients, which was consistent to its lower expression in endometrium reported earlier. SGK3 and CREB5 also showed modulated methylation level in RPL decidua.
CONCLUSION: Our finding supported that aberrant methylation of SGK1 and CREB5 could be a cause of the dysregulation of these gens in the endometrium, which is one of cause of reproductive failure. The function of SGK3 in reproduction system deserves further investigation.

Entities:  

Keywords:  Genomic DNA methylation analysis; Hi-MethySeq; Recurrent pregnancy loss; SGK gene

Mesh:

Substances:

Year:  2021        PMID: 33555507     DOI: 10.1007/s13258-020-01020-9

Source DB:  PubMed          Journal:  Genes Genomics        ISSN: 1976-9571            Impact factor:   1.839


  5 in total

1.  Association Study between Mucin 4 (MUC4) Polymorphisms and Idiopathic Recurrent Pregnancy Loss in a Korean Population.

Authors:  Ji-Hyang Kim; Han-Sung Park; Jeong-Yong Lee; Eun-Ju Ko; Young-Ran Kim; Hee-Young Cho; Woo-Sik Lee; Eun-Hee Ahn; Nam-Keun Kim
Journal:  Genes (Basel)       Date:  2022-05-24       Impact factor: 4.141

Review 2.  Stem Cell-Based Trophoblast Models to Unravel the Genetic Causes of Human Miscarriages.

Authors:  Tatiana V Nikitina; Igor N Lebedev
Journal:  Cells       Date:  2022-06-14       Impact factor: 7.666

Review 3.  DNA Methylation and Recurrent Pregnancy Loss: A Mysterious Compass?

Authors:  Qi Zhou; Yunhe Xiong; Bing Qu; Anyu Bao; Yan Zhang
Journal:  Front Immunol       Date:  2021-10-21       Impact factor: 7.561

4.  Integrated single-cell RNA-seq and DNA methylation reveal the effects of air pollution in patients with recurrent spontaneous abortion.

Authors:  Weiqiang Zhu; Yan Gu; Min Li; Zhaofeng Zhang; Junwei Liu; Yanyan Mao; Qianxi Zhu; Lin Zhao; Yupei Shen; Fujia Chen; Lingjin Xia; Lin He; Jing Du
Journal:  Clin Epigenetics       Date:  2022-08-23       Impact factor: 7.259

5.  Association of Polymorphisms in Plasminogen Activator Inhibitor-1 (PAI-1), Tissue Plasminogen Activator (tPA), and Renin (REN) with Recurrent Pregnancy Loss in Korean Women.

Authors:  Hee Young Cho; Han Sung Park; Eun Hee Ahn; Eun Ju Ko; Hyeon Woo Park; Young Ran Kim; Ji Hyang Kim; Woo Sik Lee; Nam Keun Kim
Journal:  J Pers Med       Date:  2021-12-16
  5 in total

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