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ChIP-Seq Analysis of AtfA Interactions in Aspergillus flavus Reveals Its Involvement in Aflatoxin Metabolism and Virulence Under Oxidative Stress
The risk of contamination is expanding with global warming. Targeting the pathogenicity of at its source and diminishing its colonization within the host may be a potential control strategy. Oxidative stress transcription factor AtfA plays a pivotal role in pathogenicity by combating reactive oxygen...
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Published in: | International journal of molecular sciences 2024-11, Vol.25 (22), p.12213 |
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creator | Peng, Shurui Hu, Liangbin Ge, Wei Deng, Jiakun Yao, Lishan Li, Hongbo Xu, Dan Mo, Haizhen |
description | The risk of
contamination is expanding with global warming. Targeting the pathogenicity of
at its source and diminishing its colonization within the host may be a potential control strategy. Oxidative stress transcription factor AtfA plays a pivotal role in
pathogenicity by combating reactive oxygen species (ROS) generated by host immune cells. This study employed chromatin immunoprecipitation sequencing to elucidate the binding sites and epigenetic mechanisms of AtfA under oxidative stress. Among the total 1022 identified potential AtfA-binding peaks, a 10-bp region predominated by 5'-DRTGTTGCAA-3', which is highly similar to the AP-1 binding motif was predicted. The significantly regulated genes exhibited a variety of biological functions, including regulation of filamentous growth, response to extracellular stimulus, and regulation of gene expression. Moreover, AtfA indirectly influenced these processes via the MAPK signaling pathway, carbon metabolism, and fatty acid metabolism in response to oxidative stress. The absence of
contributed to the decrease in the growth and development, sporulation, AFB
biosynthesis, and invasion ability of
under oxidative stress. These findings suggest that AtfA is critical to overcome oxidative stress induced by the host immune cells during the infection, providing a novel target for early prevention of
contamination. |
doi_str_mv | 10.3390/ijms252212213 |
format | article |
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contamination is expanding with global warming. Targeting the pathogenicity of
at its source and diminishing its colonization within the host may be a potential control strategy. Oxidative stress transcription factor AtfA plays a pivotal role in
pathogenicity by combating reactive oxygen species (ROS) generated by host immune cells. This study employed chromatin immunoprecipitation sequencing to elucidate the binding sites and epigenetic mechanisms of AtfA under oxidative stress. Among the total 1022 identified potential AtfA-binding peaks, a 10-bp region predominated by 5'-DRTGTTGCAA-3', which is highly similar to the AP-1 binding motif was predicted. The significantly regulated genes exhibited a variety of biological functions, including regulation of filamentous growth, response to extracellular stimulus, and regulation of gene expression. Moreover, AtfA indirectly influenced these processes via the MAPK signaling pathway, carbon metabolism, and fatty acid metabolism in response to oxidative stress. The absence of
contributed to the decrease in the growth and development, sporulation, AFB
biosynthesis, and invasion ability of
under oxidative stress. These findings suggest that AtfA is critical to overcome oxidative stress induced by the host immune cells during the infection, providing a novel target for early prevention of
contamination.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms252212213</identifier><identifier>PMID: 39596279</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Aflatoxins - genetics ; Aflatoxins - metabolism ; Air bases ; Aspergillus flavus - genetics ; Aspergillus flavus - metabolism ; Aspergillus flavus - pathogenicity ; Bioinformatics ; Biosynthesis ; Chromatin ; Chromatin Immunoprecipitation Sequencing ; Chromatography ; Epigenetic inheritance ; Epigenetics ; Fatty acids ; Fungal Proteins - genetics ; Fungal Proteins - metabolism ; Gene expression ; Gene Expression Regulation, Fungal ; Genes ; Kinases ; Metabolism ; Oxidative Stress ; Polyclonal antibodies ; Polypeptides ; Proteins ; Reactive oxygen species ; Reactive Oxygen Species - metabolism ; RNA polymerase ; Signal transduction ; Transcription factors ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Virulence ; Virulence - genetics</subject><ispartof>International journal of molecular sciences, 2024-11, Vol.25 (22), p.12213</ispartof><rights>COPYRIGHT 2024 MDPI AG</rights><rights>2024 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2024 by the authors. 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c369t-5a434c6db0a2df7031c36583178a5d69efe5b26b39aba115c9374e0a38e6046b3</cites><orcidid>0000-0002-2875-9065 ; 0000-0003-0747-093X ; 0000-0001-9999-6466</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3133087114/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3133087114?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25752,27923,27924,37011,37012,44589,53790,53792,74897</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39596279$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peng, Shurui</creatorcontrib><creatorcontrib>Hu, Liangbin</creatorcontrib><creatorcontrib>Ge, Wei</creatorcontrib><creatorcontrib>Deng, Jiakun</creatorcontrib><creatorcontrib>Yao, Lishan</creatorcontrib><creatorcontrib>Li, Hongbo</creatorcontrib><creatorcontrib>Xu, Dan</creatorcontrib><creatorcontrib>Mo, Haizhen</creatorcontrib><title>ChIP-Seq Analysis of AtfA Interactions in Aspergillus flavus Reveals Its Involvement in Aflatoxin Metabolism and Virulence Under Oxidative Stress</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>The risk of
contamination is expanding with global warming. Targeting the pathogenicity of
at its source and diminishing its colonization within the host may be a potential control strategy. Oxidative stress transcription factor AtfA plays a pivotal role in
pathogenicity by combating reactive oxygen species (ROS) generated by host immune cells. This study employed chromatin immunoprecipitation sequencing to elucidate the binding sites and epigenetic mechanisms of AtfA under oxidative stress. Among the total 1022 identified potential AtfA-binding peaks, a 10-bp region predominated by 5'-DRTGTTGCAA-3', which is highly similar to the AP-1 binding motif was predicted. The significantly regulated genes exhibited a variety of biological functions, including regulation of filamentous growth, response to extracellular stimulus, and regulation of gene expression. Moreover, AtfA indirectly influenced these processes via the MAPK signaling pathway, carbon metabolism, and fatty acid metabolism in response to oxidative stress. The absence of
contributed to the decrease in the growth and development, sporulation, AFB
biosynthesis, and invasion ability of
under oxidative stress. These findings suggest that AtfA is critical to overcome oxidative stress induced by the host immune cells during the infection, providing a novel target for early prevention of
contamination.</description><subject>Aflatoxins - genetics</subject><subject>Aflatoxins - metabolism</subject><subject>Air bases</subject><subject>Aspergillus flavus - genetics</subject><subject>Aspergillus flavus - metabolism</subject><subject>Aspergillus flavus - pathogenicity</subject><subject>Bioinformatics</subject><subject>Biosynthesis</subject><subject>Chromatin</subject><subject>Chromatin Immunoprecipitation Sequencing</subject><subject>Chromatography</subject><subject>Epigenetic inheritance</subject><subject>Epigenetics</subject><subject>Fatty acids</subject><subject>Fungal Proteins - genetics</subject><subject>Fungal Proteins - metabolism</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Fungal</subject><subject>Genes</subject><subject>Kinases</subject><subject>Metabolism</subject><subject>Oxidative Stress</subject><subject>Polyclonal antibodies</subject><subject>Polypeptides</subject><subject>Proteins</subject><subject>Reactive oxygen species</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RNA polymerase</subject><subject>Signal transduction</subject><subject>Transcription factors</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Virulence</subject><subject>Virulence - genetics</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNptkk1v1DAQhi0Eou3CkSuyxIVLij_yeULRqsBKRUWUcrUcZ7L1yrG3thO1P4N_XC9bShch25rR-Jl3PNYg9IaSU84b8kFvxsAKxmja_Bk6pjljGSFl9fyJf4ROQtgQwjgrmpfoiDdFU7KqOUa_lterb9kl3ODWSnMXdMBuwG0cWryyEbxUUTsbsLa4DVvwa23MFPBg5JzMd5hBmoBXMR07OzPDCDb-phMS3W3yvkKUnTM6jFjaHv_UfjJgFeAr24PHF7e6l1HPgC-jhxBeoRdD0oTXD3aBrj6d_Vh-yc4vPq-W7XmmeNnErJA5z1XZd0SyfqgIpyle1JxWtSz6soEBio6VHW9kJyktVMOrHIjkNZQkT_EF-rjX3U7dCL1K7_bSiK3Xo_R3wkktDm-svhZrN4sk1uR5KrVA7x8UvLuZIEQx6qDAGGnBTUFwynleVKzeoe_-QTdu8unH9xSpK0rzv9RaGhDaDi4VVjtR0da05rziqdEFOv0PlVYPo1bOwqBT_CAh2yco70LwMDw2SYnYDZE4GKLEv336M4_0n6nh90_Ew1Q</recordid><startdate>20241114</startdate><enddate>20241114</enddate><creator>Peng, Shurui</creator><creator>Hu, Liangbin</creator><creator>Ge, Wei</creator><creator>Deng, Jiakun</creator><creator>Yao, Lishan</creator><creator>Li, Hongbo</creator><creator>Xu, Dan</creator><creator>Mo, Haizhen</creator><general>MDPI AG</general><general>MDPI</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-2875-9065</orcidid><orcidid>https://orcid.org/0000-0003-0747-093X</orcidid><orcidid>https://orcid.org/0000-0001-9999-6466</orcidid></search><sort><creationdate>20241114</creationdate><title>ChIP-Seq Analysis of AtfA Interactions in Aspergillus flavus Reveals Its Involvement in Aflatoxin Metabolism and Virulence Under Oxidative Stress</title><author>Peng, Shurui ; 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contamination is expanding with global warming. Targeting the pathogenicity of
at its source and diminishing its colonization within the host may be a potential control strategy. Oxidative stress transcription factor AtfA plays a pivotal role in
pathogenicity by combating reactive oxygen species (ROS) generated by host immune cells. This study employed chromatin immunoprecipitation sequencing to elucidate the binding sites and epigenetic mechanisms of AtfA under oxidative stress. Among the total 1022 identified potential AtfA-binding peaks, a 10-bp region predominated by 5'-DRTGTTGCAA-3', which is highly similar to the AP-1 binding motif was predicted. The significantly regulated genes exhibited a variety of biological functions, including regulation of filamentous growth, response to extracellular stimulus, and regulation of gene expression. Moreover, AtfA indirectly influenced these processes via the MAPK signaling pathway, carbon metabolism, and fatty acid metabolism in response to oxidative stress. The absence of
contributed to the decrease in the growth and development, sporulation, AFB
biosynthesis, and invasion ability of
under oxidative stress. These findings suggest that AtfA is critical to overcome oxidative stress induced by the host immune cells during the infection, providing a novel target for early prevention of
contamination.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>39596279</pmid><doi>10.3390/ijms252212213</doi><orcidid>https://orcid.org/0000-0002-2875-9065</orcidid><orcidid>https://orcid.org/0000-0003-0747-093X</orcidid><orcidid>https://orcid.org/0000-0001-9999-6466</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Aflatoxins - genetics Aflatoxins - metabolism Air bases Aspergillus flavus - genetics Aspergillus flavus - metabolism Aspergillus flavus - pathogenicity Bioinformatics Biosynthesis Chromatin Chromatin Immunoprecipitation Sequencing Chromatography Epigenetic inheritance Epigenetics Fatty acids Fungal Proteins - genetics Fungal Proteins - metabolism Gene expression Gene Expression Regulation, Fungal Genes Kinases Metabolism Oxidative Stress Polyclonal antibodies Polypeptides Proteins Reactive oxygen species Reactive Oxygen Species - metabolism RNA polymerase Signal transduction Transcription factors Transcription Factors - genetics Transcription Factors - metabolism Virulence Virulence - genetics |
title | ChIP-Seq Analysis of AtfA Interactions in Aspergillus flavus Reveals Its Involvement in Aflatoxin Metabolism and Virulence Under Oxidative Stress |
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