Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring
Background: The births of more than 8 million infants have been enabled globally through assisted reproductive technologies (ARTs), including conventional in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) with either fresh embryo transfer (ET) or frozen embryo transfer (FET)....
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Elsevier
2020-11-01
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Series: | EBioMedicine |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S2352396420304527 |
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doaj-930022e7cbe24981adcf879e3c8e1969 |
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record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wei Chen Yong Peng Xinyi Ma Siming Kong Shuangyan Tan Yuan Wei Yangyu Zhao Wenxin Zhang Yang Wang Liying Yan Jie Qiao |
spellingShingle |
Wei Chen Yong Peng Xinyi Ma Siming Kong Shuangyan Tan Yuan Wei Yangyu Zhao Wenxin Zhang Yang Wang Liying Yan Jie Qiao Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring EBioMedicine ART ICSI Frozen embryo transfer DNA methylation Histone modifications H3K4me3 |
author_facet |
Wei Chen Yong Peng Xinyi Ma Siming Kong Shuangyan Tan Yuan Wei Yangyu Zhao Wenxin Zhang Yang Wang Liying Yan Jie Qiao |
author_sort |
Wei Chen |
title |
Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring |
title_short |
Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring |
title_full |
Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring |
title_fullStr |
Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring |
title_full_unstemmed |
Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring |
title_sort |
integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring |
publisher |
Elsevier |
series |
EBioMedicine |
issn |
2352-3964 |
publishDate |
2020-11-01 |
description |
Background: The births of more than 8 million infants have been enabled globally through assisted reproductive technologies (ARTs), including conventional in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) with either fresh embryo transfer (ET) or frozen embryo transfer (FET). However, the safety issue regarding ARTs has drawn growing attention with accumulating observations of rising health risks, and underlying epigenetic mechanisms are largely uncharacterized. Methods: In order to clarify epigenetic risks attributable to ARTs, we profiled DNA methylome on 137 umbilical cord blood (UCB) and 158 parental peripheral blood (PPB) samples, histone modifications (H3K4me3, H3K4me1, H3K27me3 and H3K27ac) on 33 UCB samples and transcriptome on 32 UCB samples by reduced representation bisulfite sequencing (RRBS), chromatin immunoprecipitation sequencing (ChIP-seq), and RNA sequencing (RNA-seq), respectively. Findings: We revealed that H3K4me3 was the most profoundly impacted by ICSI and freeze-thawing operation compared with the other three types of histone modifications. IVF-ET seemed to introduce less disturbance into infant epigenomes than IVF-FET or ICSI-ET did. ARTs also decreased the similarity of DNA methylome within twin pairs, and we confirmed that ART per se would introduce conservative changes locally through removal of parental effect. Importantly, those unique and common alterations induced by different ART procedures were highly enriched in the processes related to nervous system, cardiovascular system and glycolipid metabolism etc., which was in accordance with those findings in previous epidemiology studies and suggested some unexplored health issues, including in the immune system and skeletal system. Interpretation: Different ART procedures can induce local and functional epigenetic abnormalities, especially for DNA methylation and H3K4me3, providing an epigenetic basis for the potential long-term health risks in ART-conceived offspring. Funding sources: This study was funded by National Natural Science Foundation of China (81,730,038; 81,521,002), National Key Research and Development Program (2018YFC1004000; 2017YFA0103801; 2017YFA0105001) and Strategic Priority Research Program of the Chinese Academy of Sciences (XDA16020703). Yang Wang was supported by Postdoctoral Fellowship of Peking-Tsinghua Center for Life Science. |
topic |
ART ICSI Frozen embryo transfer DNA methylation Histone modifications H3K4me3 |
url |
http://www.sciencedirect.com/science/article/pii/S2352396420304527 |
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AT weichen integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT yongpeng integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT xinyima integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT simingkong integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT shuangyantan integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT yuanwei integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT yangyuzhao integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT wenxinzhang integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT yangwang integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT liyingyan integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring AT jieqiao integratedmultiomicsrevealepigenomicdisturbanceofassistedreproductivetechnologiesinhumanoffspring |
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spelling |
doaj-930022e7cbe24981adcf879e3c8e19692020-11-25T04:04:42ZengElsevierEBioMedicine2352-39642020-11-0161103076Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspringWei Chen0Yong Peng1Xinyi Ma2Siming Kong3Shuangyan Tan4Yuan Wei5Yangyu Zhao6Wenxin Zhang7Yang Wang8Liying Yan9Jie Qiao10Center for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, ChinaCenter for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, ChinaCenter for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, ChinaCenter for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, ChinaCenter for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.Center for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.Center for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.Center for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.Center for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Corresponding author at: Center for Reproductive Medicine of Peking University Third Hospital; NO 49 North Garden Rd., Haidian District, Beijing, 100191, ChinaCenter for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Corresponding author at: Center for Reproductive Medicine of Peking University Third Hospital; NO 49 North Garden Rd., Haidian District, Beijing, 100191, ChinaCenter for Reproductive Medicine, Department of Obstetrics and Gynecology Third Hospital,; Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.; Key Laboratory of Assisted Reproduction, Ministry of Education, Beijing 100191, China; Beijing Key Laboratory of Reproductive Endocrinology and Assisted Reproductive Technology, Beijing 100191, China; Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871, China; Beijing Advanced Innovation Center for Genomics, Peking University, Beijing 100871, China; Corresponding author at: Center for Reproductive Medicine of Peking University Third Hospital; NO 49 North Garden Rd., Haidian District, Beijing, 100191, ChinaBackground: The births of more than 8 million infants have been enabled globally through assisted reproductive technologies (ARTs), including conventional in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI) with either fresh embryo transfer (ET) or frozen embryo transfer (FET). However, the safety issue regarding ARTs has drawn growing attention with accumulating observations of rising health risks, and underlying epigenetic mechanisms are largely uncharacterized. Methods: In order to clarify epigenetic risks attributable to ARTs, we profiled DNA methylome on 137 umbilical cord blood (UCB) and 158 parental peripheral blood (PPB) samples, histone modifications (H3K4me3, H3K4me1, H3K27me3 and H3K27ac) on 33 UCB samples and transcriptome on 32 UCB samples by reduced representation bisulfite sequencing (RRBS), chromatin immunoprecipitation sequencing (ChIP-seq), and RNA sequencing (RNA-seq), respectively. Findings: We revealed that H3K4me3 was the most profoundly impacted by ICSI and freeze-thawing operation compared with the other three types of histone modifications. IVF-ET seemed to introduce less disturbance into infant epigenomes than IVF-FET or ICSI-ET did. ARTs also decreased the similarity of DNA methylome within twin pairs, and we confirmed that ART per se would introduce conservative changes locally through removal of parental effect. Importantly, those unique and common alterations induced by different ART procedures were highly enriched in the processes related to nervous system, cardiovascular system and glycolipid metabolism etc., which was in accordance with those findings in previous epidemiology studies and suggested some unexplored health issues, including in the immune system and skeletal system. Interpretation: Different ART procedures can induce local and functional epigenetic abnormalities, especially for DNA methylation and H3K4me3, providing an epigenetic basis for the potential long-term health risks in ART-conceived offspring. Funding sources: This study was funded by National Natural Science Foundation of China (81,730,038; 81,521,002), National Key Research and Development Program (2018YFC1004000; 2017YFA0103801; 2017YFA0105001) and Strategic Priority Research Program of the Chinese Academy of Sciences (XDA16020703). Yang Wang was supported by Postdoctoral Fellowship of Peking-Tsinghua Center for Life Science.http://www.sciencedirect.com/science/article/pii/S2352396420304527ARTICSIFrozen embryo transferDNA methylationHistone modificationsH3K4me3 |