Exposure to diethylhexyl phthalate (DEHP) results in a heritable modification of imprint genes DNA methylation in mouse oocytes

被引:94
作者
Li, Lan [1 ,2 ]
Zhang, Teng [1 ]
Qin, Xun-Si [1 ]
Ge, Wei [1 ]
Ma, Hua-Gang [3 ]
Sun, Li-Lan [3 ]
Hou, Zhu-Mei [1 ]
Chen, Hong [2 ]
Chen, Ping [4 ]
Qin, Guo-Qing [5 ]
Shen, Wei [1 ]
Zhang, Xi-Feng [4 ]
机构
[1] Qingdao Agr Univ, Coll Anim Sci & Technol, Lab Germ Cell Biol, Key Lab Anim Reprod & Germplasm Enhancement Univ, Qingdao 266109, Peoples R China
[2] Northwest A&F Univ, Coll Anim Sci & Technol, Shaanxi Key Lab Mol Biol Agr, Yangling 712100, Shaanxi, Peoples R China
[3] Weifang Peoples Hosp, Ctr Reprod Biol, Weifang 261041, Peoples R China
[4] Wuhan Polytech Univ, Coll Biol & Pharmaceut Engn, Wuhan 430023, Peoples R China
[5] Inno Tech Nutr Solut, Winnipeg, MB R2J 0K6, Canada
关键词
DEHP; Primordial germ cells; Oocytes; Imprint genes; DNA methylation; BISPHENOL-A; FOLLICLE FORMATION; ASSOCIATION; SPERMATOZOA; MATURATION;
D O I
10.1007/s11033-013-2967-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diethylhexyl phthalate (DEHP) is an estrogen-like compound widely used as a plasticizer in commercial products and is present in medical devices, and common household items. It is considered an endocrine disruptor since studies on experimental animals clearly show that exposure to DEHP can alter epigenetics of germ cells. This study was designed to assess the effects of DEHP on DNA methylation of imprinting genes in germ cells from fetal and adult mouse. Pregnant mice were treated with DEHP at doses of 0 and 40 mu g DEHP/kg body weight/day from 0.5 to 18.5 day post coitum. The data revealed DEHP exposure significantly reduced the percentage of methylated CpG sites in Igf2r and Peg3 differentially methylated regions (DMRs) in primordial germ cells from female and male fetal mouse, particularly, in the oocytes of 21 dpp mice (F1), which were produced by the pregnant micetreated with DEHP. More surprisingly, the modification of the DNA methylation of imprinted genes in F1 mouse oocytes was heritable to F2 offspring which exhibit lower percentages of methylated CpG sites in imprinted genes DMRs. In conclusion, DEHP exposure can affect the DNA methylation of imprinting genes not only in fetal mouse germ cells and growing oocytes, but also in offspring's oocytes.
引用
收藏
页码:1227 / 1235
页数:9
相关论文
共 26 条
[1]   In Vitro Acute Exposure to DEHP Affects Oocyte Meiotic Maturation, Energy and Oxidative Stress Parameters in a Large Animal Model [J].
Ambruosi, Barbara ;
Uranio, Manuel Filioli ;
Sardanelli, Anna Maria ;
Pocar, Paola ;
Martino, Nicola Antonio ;
Paternoster, Maria Stefania ;
Amati, Francesca ;
Dell'Aquila, Maria Elena .
PLOS ONE, 2011, 6 (11)
[2]   Epigenetic responses following maternal dietary exposure to physiologically relevant levels of bisphenol A [J].
Anderson, Olivia S. ;
Nahar, Muna S. ;
Faulk, Christopher ;
Jones, Tamara R. ;
Liao, Chunyang ;
Kannan, Kurunthachalam ;
Weinhouse, Caren ;
Rozek, Laura S. ;
Dolinoy, Dana C. .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 2012, 53 (05) :334-342
[3]   Variability of Urinary Phthalate Metabolite and Bisphenol A Concentrations before and during Pregnancy [J].
Braun, Joe M. ;
Smith, Kristen W. ;
Williams, Paige L. ;
Calafat, Antonia M. ;
Berry, Katharine ;
Ehrlich, Shelley ;
Hauser, Russ .
ENVIRONMENTAL HEALTH PERSPECTIVES, 2012, 120 (05) :739-745
[4]   Bisphenol-A exposure in utero leads to epigenetic alterations in the developmental programming of uterine estrogen response [J].
Bromer, Jason G. ;
Zhou, Yuping ;
Taylor, Melissa B. ;
Doherty, Leo ;
Taylor, Hugh S. .
FASEB JOURNAL, 2010, 24 (07) :2273-2280
[5]   DEHP Impairs Zebrafish Reproduction by Affecting Critical Factors in Oogenesis [J].
Carnevali, Oliana ;
Tosti, Luca ;
Speciale, Claudia ;
Peng, Chun ;
Zhu, Yong ;
Maradonna, Francesca .
PLOS ONE, 2010, 5 (04)
[6]   Bisphenol A exposure modifies methylation of imprinted genes in mouse oocytes via the estrogen receptor signaling pathway [J].
Chao, Hu-He ;
Zhang, Xi-Feng ;
Chen, Bo ;
Pan, Bo ;
Zhang, Lian-Jun ;
Li, Lan ;
Sun, Xiao-Feng ;
Shi, Qing-Hua ;
Shen, Wei .
HISTOCHEMISTRY AND CELL BIOLOGY, 2012, 137 (02) :249-259
[7]   Effect of mono-(2-ethylhexyl) phthalate (MEHP) on resumption of meiosis, in vitro maturation and embryo development of immature mouse oocytes [J].
Dalman, A. ;
Eimani, H. ;
Sepehri, H. ;
Ashtiani, S. K. ;
Valojerdi, M. R. ;
Eftekhari-Yazdi, P. ;
Shahverdi, A. .
BIOFACTORS, 2008, 33 (02) :149-155
[8]   Maternal nutrient supplementation counteracts bisphenol A-induced DNA hypomethylation in early development [J].
Dolinoy, Dana C. ;
Huang, Dale ;
Jirtle, Randy L. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (32) :13056-13061
[9]   Aberrant DNA methylation at Igf2-H19 imprinting control region in spermatozoa upon neonatal exposure to bisphenol A and its association with post implantation loss [J].
Doshi, Tanvi ;
D'souza, Criselle ;
Vanage, Geeta .
MOLECULAR BIOLOGY REPORTS, 2013, 40 (08) :4747-4757
[10]   Bisphenol A alters early oogenesis and follicle formation in the fetal ovary of the rhesus monkey [J].
Hunt, Patricia A. ;
Lawson, Crystal ;
Gieske, Mary ;
Murdoch, Brenda ;
Smith, Helen ;
Marre, Alyssa ;
Hassold, Terry ;
VandeVoort, Catherine A. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (43) :17525-17530