A novel regulatory network among LncRpa, CircRar1, MiR-671 and apoptotic genes promotes lead-induced neuronal cell apoptosis

Aruo Nan; Lijian Chen; Nan Zhang; Zhenzhong Liu; Ti Yang; Zhishan Wang; Chengfeng Yang; Yiguo Jiang

doi:10.1007/s00204-016-1837-1

A novel regulatory network among LncRpa, CircRar1, MiR-671 and apoptotic genes promotes lead-induced neuronal cell apoptosis

Aruo Nan, Lijian Chen, Nan Zhang, Zhenzhong Liu, Ti Yang, Zhishan Wang, Chengfeng Yang, Yiguo Jiang

Markey Cancer Center / Cancer Research Priority Initiative

Producción científica: Article › revisión exhaustiva

103 Citas (Scopus)

Resumen

Lead is a metal that has toxic effects on the developing nervous system. However, the mechanisms underlying lead-induced neurotoxicity are not well understood. Non-coding RNAs (ncRNAs) play an important role in epigenetic regulation, but few studies have examined the function of ncRNAs in lead-induced neurotoxicity. We addressed this in the present study by evaluating the functions of a long non-coding RNA (named lncRpa) and a circular RNA (named circRar1) in a mouse model of lead-induced neurotoxicity. High-throughput RNA sequencing showed that both lncRpa and circRar1 promoted neuronal apoptosis. We also found that lncRpa and circRar1 induced the upregulation of apoptosis-associated factors caspase8 and p38 at the mRNA and protein levels via modulation of their common target microRNA miR-671. This is the first report of a regulatory interaction among a lncRNA, circRNA, and miRNA mediating neuronal apoptosis in response to lead toxicity.

Idioma original	English
Páginas (desde-hasta)	1671-1684
Número de páginas	14
Publicación	Archives of Toxicology
Volumen	91
N.º	4
DOI	https://doi.org/10.1007/s00204-016-1837-1
Estado	Published - abr 1 2017

Nota bibliográfica

Publisher Copyright:
© 2016, The Author(s).

Financiación

We thank Dr. Sijin Liu (professor of Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences) for recommendations on the manuscript. This work was supported by the National Key Basic Research Program of China (No. 2012CB525004 to Y. G. J.), the National Natural Science Foundation of China (No. 21277036, 81573180, and 81172633 to Y. G. J.), the Key Program of Guangdong Natural Science Foundation (No. 2014A030311017 to Y. G. J.), the University Major Program of Guangdong (No. 2014SZD48 to Y. G. J.), the University Talent Program of Guangdong (No. 2013-164 to Y. G. J.), and the University Chief Scientist Program of Guangzhou (No. 1201541575 to Y. G. J.).

Financiadores	Número del financiador
University Chief Scientist Program of Guangzhou	1201541575
University Major Program of Guangdong	2014SZD48
University Talent Program of Guangdong	2013-164
National Natural Science Foundation of China (NSFC)	81573180, 81172633, 21277036
National Natural Science Foundation of China (NSFC)
Natural Science Foundation of Guangdong Province	2014A030311017
Natural Science Foundation of Guangdong Province
National Key Basic Research and Development Program of China	2012CB525004
National Key Basic Research and Development Program of China

ASJC Scopus subject areas

Toxicology
Health, Toxicology and Mutagenesis

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abstract = "Lead is a metal that has toxic effects on the developing nervous system. However, the mechanisms underlying lead-induced neurotoxicity are not well understood. Non-coding RNAs (ncRNAs) play an important role in epigenetic regulation, but few studies have examined the function of ncRNAs in lead-induced neurotoxicity. We addressed this in the present study by evaluating the functions of a long non-coding RNA (named lncRpa) and a circular RNA (named circRar1) in a mouse model of lead-induced neurotoxicity. High-throughput RNA sequencing showed that both lncRpa and circRar1 promoted neuronal apoptosis. We also found that lncRpa and circRar1 induced the upregulation of apoptosis-associated factors caspase8 and p38 at the mRNA and protein levels via modulation of their common target microRNA miR-671. This is the first report of a regulatory interaction among a lncRNA, circRNA, and miRNA mediating neuronal apoptosis in response to lead toxicity.",

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author = "Aruo Nan and Lijian Chen and Nan Zhang and Zhenzhong Liu and Ti Yang and Zhishan Wang and Chengfeng Yang and Yiguo Jiang",

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AU - Nan, Aruo

AU - Chen, Lijian

AU - Zhang, Nan

AU - Liu, Zhenzhong

AU - Yang, Ti

AU - Wang, Zhishan

AU - Yang, Chengfeng

AU - Jiang, Yiguo

PY - 2017/4/1

Y1 - 2017/4/1

N2 - Lead is a metal that has toxic effects on the developing nervous system. However, the mechanisms underlying lead-induced neurotoxicity are not well understood. Non-coding RNAs (ncRNAs) play an important role in epigenetic regulation, but few studies have examined the function of ncRNAs in lead-induced neurotoxicity. We addressed this in the present study by evaluating the functions of a long non-coding RNA (named lncRpa) and a circular RNA (named circRar1) in a mouse model of lead-induced neurotoxicity. High-throughput RNA sequencing showed that both lncRpa and circRar1 promoted neuronal apoptosis. We also found that lncRpa and circRar1 induced the upregulation of apoptosis-associated factors caspase8 and p38 at the mRNA and protein levels via modulation of their common target microRNA miR-671. This is the first report of a regulatory interaction among a lncRNA, circRNA, and miRNA mediating neuronal apoptosis in response to lead toxicity.

AB - Lead is a metal that has toxic effects on the developing nervous system. However, the mechanisms underlying lead-induced neurotoxicity are not well understood. Non-coding RNAs (ncRNAs) play an important role in epigenetic regulation, but few studies have examined the function of ncRNAs in lead-induced neurotoxicity. We addressed this in the present study by evaluating the functions of a long non-coding RNA (named lncRpa) and a circular RNA (named circRar1) in a mouse model of lead-induced neurotoxicity. High-throughput RNA sequencing showed that both lncRpa and circRar1 promoted neuronal apoptosis. We also found that lncRpa and circRar1 induced the upregulation of apoptosis-associated factors caspase8 and p38 at the mRNA and protein levels via modulation of their common target microRNA miR-671. This is the first report of a regulatory interaction among a lncRNA, circRNA, and miRNA mediating neuronal apoptosis in response to lead toxicity.

KW - Cell apoptosis

KW - CircRNA

KW - Lead

KW - LncRNA

KW - MiRNA

KW - Neurotoxicity

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A novel regulatory network among LncRpa, CircRar1, MiR-671 and apoptotic genes promotes lead-induced neuronal cell apoptosis

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Nota bibliográfica

Financiación

ASJC Scopus subject areas

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