Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure

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Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure. / Zhang, Zhonghao; Wang, Jiankang; Shi, Fuquan; Li, Yingqing; Zou, Peng; Tang, Ying; Liu, Chang; Wang, Yimeng; Ling, Xi; Sun, Lei; Liu, Cuiqing; Zhang, Yanshu; Gao, Fei; Chen, Qing; Ao, Lin; Han, Fei; Liu, Jinyi; Cao, Jia.

In: Environment International, Vol. 169, 107544, 2022.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Zhang, Z, Wang, J, Shi, F, Li, Y, Zou, P, Tang, Y, Liu, C, Wang, Y, Ling, X, Sun, L, Liu, C, Zhang, Y, Gao, F, Chen, Q, Ao, L, Han, F, Liu, J & Cao, J 2022, 'Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure', Environment International, vol. 169, 107544. https://doi.org/10.1016/j.envint.2022.107544

APA

Zhang, Z., Wang, J., Shi, F., Li, Y., Zou, P., Tang, Y., Liu, C., Wang, Y., Ling, X., Sun, L., Liu, C., Zhang, Y., Gao, F., Chen, Q., Ao, L., Han, F., Liu, J., & Cao, J. (2022). Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure. Environment International, 169, [107544]. https://doi.org/10.1016/j.envint.2022.107544

Vancouver

Zhang Z, Wang J, Shi F, Li Y, Zou P, Tang Y et al. Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure. Environment International. 2022;169. 107544. https://doi.org/10.1016/j.envint.2022.107544

Author

Zhang, Zhonghao ; Wang, Jiankang ; Shi, Fuquan ; Li, Yingqing ; Zou, Peng ; Tang, Ying ; Liu, Chang ; Wang, Yimeng ; Ling, Xi ; Sun, Lei ; Liu, Cuiqing ; Zhang, Yanshu ; Gao, Fei ; Chen, Qing ; Ao, Lin ; Han, Fei ; Liu, Jinyi ; Cao, Jia. / Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure. In: Environment International. 2022 ; Vol. 169.

Bibtex

@article{c4e0f0aeab5643eb85ee3e86c00bcc5b,
title = "Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure",
abstract = "The effects of ambient fine particles on male reproductive health have raised widespread concern. The particular underlying mechanisms of the damage remain largely unclear and demand more research in new directions. Previous research has revealed that DNA methylation plays an important role in male reproductive development and is also vulnerable to environmental influences. However, there hasn't been enough investigation into the involvement of DNA methylation in PM2.5-induced male reproductive toxicity. Here, we establish a real-time PM2.5 exposure model and revealed that PM2.5 exposure could lead to testicular dysfunction including spermatogenesis impairment and steroid hormone dysfunction. In particular, the decrease in the testicular global level of 5-methylcytosine (5mC) indicated a possible association of DNA methylation with testicular injury induced by PM2.5 exposure. Further genome-wide methylation analysis revealed genomic hypomethylation of testicular DNA and identified more than 1000 differentially methylated regions in both CAP and UA versus FA, indicating that PM2.5 exposure, even low-dose, could modulate the testicular methylome. Furthermore, integrated analysis of methylome and transcriptome identified some key methylated genes and networks, which may be involved in spermatogenesis and synthesis of steroid hormone. The testicular methylation levels of key genes especially Cyp11a1 and Pax8 raised, and their consequent reduced expression may impair the testosterone and sperm production process. Our research provides fundamental knowledge as well as novel insights into the possible involvement of DNA methylation in PM2.5-induced male reproductive harm.",
keywords = "DNA methylome, Male reproductive system, PM, Spermatogenesis",
author = "Zhonghao Zhang and Jiankang Wang and Fuquan Shi and Yingqing Li and Peng Zou and Ying Tang and Chang Liu and Yimeng Wang and Xi Ling and Lei Sun and Cuiqing Liu and Yanshu Zhang and Fei Gao and Qing Chen and Lin Ao and Fei Han and Jinyi Liu and Jia Cao",
note = "Publisher Copyright: {\textcopyright} 2022",
year = "2022",
doi = "10.1016/j.envint.2022.107544",
language = "English",
volume = "169",
journal = "Environment international",
issn = "0160-4120",
publisher = "Pergamon Press",

}

RIS

TY - JOUR

T1 - Genome-wide alternation and effect of DNA methylation in the impairments of steroidogenesis and spermatogenesis after PM2.5 exposure

AU - Zhang, Zhonghao

AU - Wang, Jiankang

AU - Shi, Fuquan

AU - Li, Yingqing

AU - Zou, Peng

AU - Tang, Ying

AU - Liu, Chang

AU - Wang, Yimeng

AU - Ling, Xi

AU - Sun, Lei

AU - Liu, Cuiqing

AU - Zhang, Yanshu

AU - Gao, Fei

AU - Chen, Qing

AU - Ao, Lin

AU - Han, Fei

AU - Liu, Jinyi

AU - Cao, Jia

N1 - Publisher Copyright: © 2022

PY - 2022

Y1 - 2022

N2 - The effects of ambient fine particles on male reproductive health have raised widespread concern. The particular underlying mechanisms of the damage remain largely unclear and demand more research in new directions. Previous research has revealed that DNA methylation plays an important role in male reproductive development and is also vulnerable to environmental influences. However, there hasn't been enough investigation into the involvement of DNA methylation in PM2.5-induced male reproductive toxicity. Here, we establish a real-time PM2.5 exposure model and revealed that PM2.5 exposure could lead to testicular dysfunction including spermatogenesis impairment and steroid hormone dysfunction. In particular, the decrease in the testicular global level of 5-methylcytosine (5mC) indicated a possible association of DNA methylation with testicular injury induced by PM2.5 exposure. Further genome-wide methylation analysis revealed genomic hypomethylation of testicular DNA and identified more than 1000 differentially methylated regions in both CAP and UA versus FA, indicating that PM2.5 exposure, even low-dose, could modulate the testicular methylome. Furthermore, integrated analysis of methylome and transcriptome identified some key methylated genes and networks, which may be involved in spermatogenesis and synthesis of steroid hormone. The testicular methylation levels of key genes especially Cyp11a1 and Pax8 raised, and their consequent reduced expression may impair the testosterone and sperm production process. Our research provides fundamental knowledge as well as novel insights into the possible involvement of DNA methylation in PM2.5-induced male reproductive harm.

AB - The effects of ambient fine particles on male reproductive health have raised widespread concern. The particular underlying mechanisms of the damage remain largely unclear and demand more research in new directions. Previous research has revealed that DNA methylation plays an important role in male reproductive development and is also vulnerable to environmental influences. However, there hasn't been enough investigation into the involvement of DNA methylation in PM2.5-induced male reproductive toxicity. Here, we establish a real-time PM2.5 exposure model and revealed that PM2.5 exposure could lead to testicular dysfunction including spermatogenesis impairment and steroid hormone dysfunction. In particular, the decrease in the testicular global level of 5-methylcytosine (5mC) indicated a possible association of DNA methylation with testicular injury induced by PM2.5 exposure. Further genome-wide methylation analysis revealed genomic hypomethylation of testicular DNA and identified more than 1000 differentially methylated regions in both CAP and UA versus FA, indicating that PM2.5 exposure, even low-dose, could modulate the testicular methylome. Furthermore, integrated analysis of methylome and transcriptome identified some key methylated genes and networks, which may be involved in spermatogenesis and synthesis of steroid hormone. The testicular methylation levels of key genes especially Cyp11a1 and Pax8 raised, and their consequent reduced expression may impair the testosterone and sperm production process. Our research provides fundamental knowledge as well as novel insights into the possible involvement of DNA methylation in PM2.5-induced male reproductive harm.

KW - DNA methylome

KW - Male reproductive system

KW - PM

KW - Spermatogenesis

U2 - 10.1016/j.envint.2022.107544

DO - 10.1016/j.envint.2022.107544

M3 - Journal article

C2 - 36174482

AN - SCOPUS:85138804390

VL - 169

JO - Environment international

JF - Environment international

SN - 0160-4120

M1 - 107544

ER -

ID: 322644629