An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest

Precision toxicology evaluates the toxicity of certain substances by isolating a small group of cells with a typical phenotype of interest followed by a single cell sequencing-based analysis. In this in vitro attempt, ochratoxin A (OTA), a typical mycotoxin and food contaminant, is found to induce G...

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Main Authors: Boyang Zhang, Liye Zhu, Yaqi Dai, Hongyu Li, Kunlun Huang, Yunbo Luo, Wentao Xu
Format: Article
Language:English
Published: Taylor & Francis Group 2020-02-01
Series:Epigenetics
Subjects:
Online Access:http://dx.doi.org/10.1080/15592294.2019.1644878
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author Boyang Zhang
Liye Zhu
Yaqi Dai
Hongyu Li
Kunlun Huang
Yunbo Luo
Wentao Xu
author_facet Boyang Zhang
Liye Zhu
Yaqi Dai
Hongyu Li
Kunlun Huang
Yunbo Luo
Wentao Xu
author_sort Boyang Zhang
collection DOAJ
description Precision toxicology evaluates the toxicity of certain substances by isolating a small group of cells with a typical phenotype of interest followed by a single cell sequencing-based analysis. In this in vitro attempt, ochratoxin A (OTA), a typical mycotoxin and food contaminant, is found to induce G0/G1 phase cell cycle arrest in human renal proximal tubular HKC cells at a concentration of 20 μM after a 24h-treatment. A small number of G0/G1 phase HKC cells are evaluated in both the presence and absence of OTA. These cells are sorted with a flow cytometer and subjected to mRNA and DNA methylation sequencing using Smart-Seq2 and single-cell reduced-representation bisulfite sequencing (scRRBS) technology, respectively. Integrated analysis of the transcriptome and methylome profiles reveals that OTA causes abnormal expression of the essential genes that regulate G1/S phase transition, act as signal transductors in G1 DNA damage checkpoints, and associate with the anaphase-promoting complex/cyclosome. The alteration of their DNA methylation status is a significant underlying epigenetic mechanism. Furthermore, Notch signaling and Ras/MAPK/CREB pathways are found to be suppressed by OTA. This attempt at precision toxicology paves the way for a deeper understanding of OTA toxicity and provides an innovative strategy to researchers in the toxicology and pharmacology field.
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spelling doaj.art-171a2b59a27e4918af0c65962e6211192023-09-21T13:09:22ZengTaylor & Francis GroupEpigenetics1559-22941559-23082020-02-01151-219921410.1080/15592294.2019.16448781644878An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrestBoyang Zhang0Liye Zhu1Yaqi Dai2Hongyu Li3Kunlun Huang4Yunbo Luo5Wentao Xu6College of Food Science and Nutritional Engineering, China Agricultural UniversityCollege of Food Science and Nutritional Engineering, China Agricultural UniversityCollege of Food Science and Nutritional Engineering, China Agricultural UniversityCollege of Food Science and Nutritional Engineering, China Agricultural UniversityCollege of Food Science and Nutritional Engineering, China Agricultural UniversityCollege of Food Science and Nutritional Engineering, China Agricultural UniversityCollege of Food Science and Nutritional Engineering, China Agricultural UniversityPrecision toxicology evaluates the toxicity of certain substances by isolating a small group of cells with a typical phenotype of interest followed by a single cell sequencing-based analysis. In this in vitro attempt, ochratoxin A (OTA), a typical mycotoxin and food contaminant, is found to induce G0/G1 phase cell cycle arrest in human renal proximal tubular HKC cells at a concentration of 20 μM after a 24h-treatment. A small number of G0/G1 phase HKC cells are evaluated in both the presence and absence of OTA. These cells are sorted with a flow cytometer and subjected to mRNA and DNA methylation sequencing using Smart-Seq2 and single-cell reduced-representation bisulfite sequencing (scRRBS) technology, respectively. Integrated analysis of the transcriptome and methylome profiles reveals that OTA causes abnormal expression of the essential genes that regulate G1/S phase transition, act as signal transductors in G1 DNA damage checkpoints, and associate with the anaphase-promoting complex/cyclosome. The alteration of their DNA methylation status is a significant underlying epigenetic mechanism. Furthermore, Notch signaling and Ras/MAPK/CREB pathways are found to be suppressed by OTA. This attempt at precision toxicology paves the way for a deeper understanding of OTA toxicity and provides an innovative strategy to researchers in the toxicology and pharmacology field.http://dx.doi.org/10.1080/15592294.2019.1644878precision toxicologysingle-cell sequencingcell cycle arrestdna methylationochratoxin a
spellingShingle Boyang Zhang
Liye Zhu
Yaqi Dai
Hongyu Li
Kunlun Huang
Yunbo Luo
Wentao Xu
An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest
Epigenetics
precision toxicology
single-cell sequencing
cell cycle arrest
dna methylation
ochratoxin a
title An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest
title_full An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest
title_fullStr An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest
title_full_unstemmed An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest
title_short An in vitro attempt at precision toxicology reveals the involvement of DNA methylation alteration in ochratoxin A-induced G0/G1 phase arrest
title_sort in vitro attempt at precision toxicology reveals the involvement of dna methylation alteration in ochratoxin a induced g0 g1 phase arrest
topic precision toxicology
single-cell sequencing
cell cycle arrest
dna methylation
ochratoxin a
url http://dx.doi.org/10.1080/15592294.2019.1644878
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