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母猴体重会影响普通狨猴(绢毛猴)中参与代谢途径的基因的胎盘DNA甲基化。

Maternal weight affects placental DNA methylation of genes involved in metabolic pathways in the common marmoset monkey (Callithrix jacchus).

作者信息

Narapareddy Laren, Wildman Derek E, Armstrong Don L, Weckle Amy, Bell Aleeca F, Patil Crystal L, Tardif Suzette D, Ross Corinna N, Rutherford Julienne N

机构信息

Nell Hodgson Woodruff School of Nursing, Emory University, Atlanta, Georgia.

Genomics Program, College of Public Health, University of South Florida, Tampa, Florida.

出版信息

Am J Primatol. 2020 Mar;82(3):e23101. doi: 10.1002/ajp.23101. Epub 2020 Feb 5.

DOI:10.1002/ajp.23101
PMID:32020652
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7154656/
Abstract

Accumulating evidence suggests that dysregulation of placental DNA methylation (DNAm) is a mechanism linking maternal weight during pregnancy to metabolic programming outcomes. The common marmoset, Callithrix jaccus, is a platyrrhine primate species that has provided much insight into studies of the primate placenta, maternal condition, and metabolic programming, yet the relationships between maternal weight and placental DNAm are unknown. Here, we report genome-wide DNAm from term marmoset placentas using reduced representation bisulfite sequencing. We identified 74 genes whose DNAm pattern is associated with maternal weight during gestation. These genes are predominantly involved in energy metabolism and homeostasis, including the regulation of glycolytic and lipid metabolic processes pathways.

摘要

越来越多的证据表明,胎盘DNA甲基化(DNAm)失调是一种将孕期母体体重与代谢编程结果联系起来的机制。普通狨猴(Callithrix jaccus)是一种阔鼻猴灵长类动物,为灵长类胎盘、母体状况和代谢编程的研究提供了很多见解,但母体体重与胎盘DNAm之间的关系尚不清楚。在这里,我们使用简化代表性亚硫酸氢盐测序报告了足月狨猴胎盘的全基因组DNAm。我们鉴定出74个基因,其DNAm模式与孕期母体体重相关。这些基因主要参与能量代谢和体内平衡,包括糖酵解和脂质代谢过程途径的调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/574c258e922f/AJP-82-e23101-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/4897314da329/AJP-82-e23101-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/b14bdbedec84/AJP-82-e23101-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/ebb0e42b90d8/AJP-82-e23101-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/7125f2b1f437/AJP-82-e23101-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/574c258e922f/AJP-82-e23101-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/4897314da329/AJP-82-e23101-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/b14bdbedec84/AJP-82-e23101-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/ebb0e42b90d8/AJP-82-e23101-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/7125f2b1f437/AJP-82-e23101-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6375/7154656/574c258e922f/AJP-82-e23101-g005.jpg

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2
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J Lipid Res. 2017 Feb;58(2):443-454. doi: 10.1194/jlr.P072355. Epub 2016 Dec 2.
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胎盘低甲基化在缺乏逆转录元件的基因组位点中更为明显。
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