Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation

Retinoic acid-inducible gene I (RIG-I) serves as an essential viral RNA sensor for innate immune. The activation of the RIG-I-like receptors (RLRs) pathway triggers many regulations for the outcome of type I interferon, including ubiquitination, dephosphorylation, ISGylation, and autophagy. However,...

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Main Authors: Shaotang Ye, Chen Tan, Xiaoyun Yang, Ji Wang, Qi Li, Liang Xu, Zhen Wang, Jianwei Mao, Jingyu Wang, Kui Cheng, Aolei Chen, Pei Zhou, Shoujun Li
Format: Article
Language:English
Published: MDPI AG 2022-06-01
Series:Cells
Subjects:
Online Access:https://www.mdpi.com/2073-4409/11/13/2009
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author Shaotang Ye
Chen Tan
Xiaoyun Yang
Ji Wang
Qi Li
Liang Xu
Zhen Wang
Jianwei Mao
Jingyu Wang
Kui Cheng
Aolei Chen
Pei Zhou
Shoujun Li
author_facet Shaotang Ye
Chen Tan
Xiaoyun Yang
Ji Wang
Qi Li
Liang Xu
Zhen Wang
Jianwei Mao
Jingyu Wang
Kui Cheng
Aolei Chen
Pei Zhou
Shoujun Li
author_sort Shaotang Ye
collection DOAJ
description Retinoic acid-inducible gene I (RIG-I) serves as an essential viral RNA sensor for innate immune. The activation of the RIG-I-like receptors (RLRs) pathway triggers many regulations for the outcome of type I interferon, including ubiquitination, dephosphorylation, ISGylation, and autophagy. However, the autophagy-related regulation of RIG-I is still not fully understood. To investigate the potentially unknown genes related to autophagy-related regulation of RIG-I, we firstly confirm the induction of autophagy derived by overexpression of RIG-I. Furthermore, the autophagy inducer and inhibitor drugs were used in different assays. The results showed autophagy could control the activation of RLRs pathway and expression of exogenous RIG-I. In addition, we carried out the transcriptome analysis of overexpression of RIG-I in vitro. Differentially expressed genes (DEGs) in GO and KEGG signaling pathways enrichment provided a newly complex network. Finally, the validation of qPCR indicated that the DEGs PTPN22, PRKN, OTUD7B, and SIRT2 were correlated to the negative regulation of excessive expression of RIG-I. Taken together, our study contributed new insights into a more comprehensive understanding of the regulation of excessive expression of RIG-I. It provided the potential candidate genes for autophagy-related negative regulation for further investigation.
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spelling doaj.art-920e43734b4f4e27bd6ff69eb73739822023-11-23T19:48:01ZengMDPI AGCells2073-44092022-06-011113200910.3390/cells11132009Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative RegulationShaotang Ye0Chen Tan1Xiaoyun Yang2Ji Wang3Qi Li4Liang Xu5Zhen Wang6Jianwei Mao7Jingyu Wang8Kui Cheng9Aolei Chen10Pei Zhou11Shoujun Li12College of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaLanzhou Veterinary Research Institute, Chinese Academy of Agricultural Science, Lanzhou 730046, ChinaZhaoqing Institute of Biotechnology Co., Ltd., Zhaoqing 526000, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaCollege of Veterinary Medicine, South China Agricultural University, Guangzhou 510642, ChinaRetinoic acid-inducible gene I (RIG-I) serves as an essential viral RNA sensor for innate immune. The activation of the RIG-I-like receptors (RLRs) pathway triggers many regulations for the outcome of type I interferon, including ubiquitination, dephosphorylation, ISGylation, and autophagy. However, the autophagy-related regulation of RIG-I is still not fully understood. To investigate the potentially unknown genes related to autophagy-related regulation of RIG-I, we firstly confirm the induction of autophagy derived by overexpression of RIG-I. Furthermore, the autophagy inducer and inhibitor drugs were used in different assays. The results showed autophagy could control the activation of RLRs pathway and expression of exogenous RIG-I. In addition, we carried out the transcriptome analysis of overexpression of RIG-I in vitro. Differentially expressed genes (DEGs) in GO and KEGG signaling pathways enrichment provided a newly complex network. Finally, the validation of qPCR indicated that the DEGs PTPN22, PRKN, OTUD7B, and SIRT2 were correlated to the negative regulation of excessive expression of RIG-I. Taken together, our study contributed new insights into a more comprehensive understanding of the regulation of excessive expression of RIG-I. It provided the potential candidate genes for autophagy-related negative regulation for further investigation.https://www.mdpi.com/2073-4409/11/13/2009RIG-Ioverexpressionautophagynegative regulationtranscriptome analysis
spellingShingle Shaotang Ye
Chen Tan
Xiaoyun Yang
Ji Wang
Qi Li
Liang Xu
Zhen Wang
Jianwei Mao
Jingyu Wang
Kui Cheng
Aolei Chen
Pei Zhou
Shoujun Li
Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation
Cells
RIG-I
overexpression
autophagy
negative regulation
transcriptome analysis
title Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation
title_full Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation
title_fullStr Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation
title_full_unstemmed Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation
title_short Transcriptome Analysis of Retinoic Acid-Inducible Gene I Overexpression Reveals the Potential Genes for Autophagy-Related Negative Regulation
title_sort transcriptome analysis of retinoic acid inducible gene i overexpression reveals the potential genes for autophagy related negative regulation
topic RIG-I
overexpression
autophagy
negative regulation
transcriptome analysis
url https://www.mdpi.com/2073-4409/11/13/2009
work_keys_str_mv AT shaotangye transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT chentan transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT xiaoyunyang transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT jiwang transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT qili transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT liangxu transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT zhenwang transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT jianweimao transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT jingyuwang transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT kuicheng transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT aoleichen transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT peizhou transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation
AT shoujunli transcriptomeanalysisofretinoicacidinduciblegeneioverexpressionrevealsthepotentialgenesforautophagyrelatednegativeregulation