揭示鱼类免疫细胞冷应激反应中染色质介导的转录调控网络。

IF 7.9 2区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Journal of Genetics and Genomics Pub Date : 2025-08-01 Epub Date: 2025-01-21 DOI:10.1016/j.jgg.2025.01.008
He Jiao, Songqian Huang, Minghao Zhang, Qiao Huang, Chenyu Yan, Jingting Qi, Jiangbo Cheng, Yuan Xu, Xue Zhai, Xinwen Li, Siyao Zhan, Wei Li, Zhichao Wu, Jiulin Chan, Liangbiao Chen, Peng Hu
{"title":"揭示鱼类免疫细胞冷应激反应中染色质介导的转录调控网络。","authors":"He Jiao, Songqian Huang, Minghao Zhang, Qiao Huang, Chenyu Yan, Jingting Qi, Jiangbo Cheng, Yuan Xu, Xue Zhai, Xinwen Li, Siyao Zhan, Wei Li, Zhichao Wu, Jiulin Chan, Liangbiao Chen, Peng Hu","doi":"10.1016/j.jgg.2025.01.008","DOIUrl":null,"url":null,"abstract":"<p><p>Temperature fluctuations challenge ectothermic species, particularly tropical fish dependent on external temperatures for physiological regulation. However, the molecular mechanisms through which low-temperature stress impacts immune responses in these species, especially in relation to chromatin accessibility and epigenetic regulation, remain poorly understood. In this study, we investigate chromatin and transcriptional changes in the head kidney and thymus tissues of Nile tilapia (Oreochromis niloticus), a tropical fish of significant economic importance, under cold stress. By analyzing cis-regulatory elements in open chromatin regions and their associated transcription factors (TFs), we construct a comprehensive transcriptional regulatory network (TRN) governing immune responses, including DNA damage-induced apoptosis. Our analysis identifies 119 TFs within the TRN, with Stat1 emerging as a central hub exhibiting distinct binding dynamics under cold stress, as revealed by footprint analysis. Overexpression of Stat1 in immune cells leads to apoptosis and increases the expression of apoptosis-related genes, many of which contain Stat1-binding sites in their regulatory regions, emphasizing its critical role in immune cell survival during cold stress. These results provide insights into the transcriptional and epigenetic regulation of immune responses to cold stress in tilapia and highlight Stat1 as a promising target for enhancing cold tolerance in tropical fish species.</p>","PeriodicalId":54825,"journal":{"name":"Journal of Genetics and Genomics","volume":" ","pages":"1046-1057"},"PeriodicalIF":7.9000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Uncovering the chromatin-mediated transcriptional regulatory network governing cold stress responses in fish immune cells.\",\"authors\":\"He Jiao, Songqian Huang, Minghao Zhang, Qiao Huang, Chenyu Yan, Jingting Qi, Jiangbo Cheng, Yuan Xu, Xue Zhai, Xinwen Li, Siyao Zhan, Wei Li, Zhichao Wu, Jiulin Chan, Liangbiao Chen, Peng Hu\",\"doi\":\"10.1016/j.jgg.2025.01.008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Temperature fluctuations challenge ectothermic species, particularly tropical fish dependent on external temperatures for physiological regulation. However, the molecular mechanisms through which low-temperature stress impacts immune responses in these species, especially in relation to chromatin accessibility and epigenetic regulation, remain poorly understood. In this study, we investigate chromatin and transcriptional changes in the head kidney and thymus tissues of Nile tilapia (Oreochromis niloticus), a tropical fish of significant economic importance, under cold stress. By analyzing cis-regulatory elements in open chromatin regions and their associated transcription factors (TFs), we construct a comprehensive transcriptional regulatory network (TRN) governing immune responses, including DNA damage-induced apoptosis. Our analysis identifies 119 TFs within the TRN, with Stat1 emerging as a central hub exhibiting distinct binding dynamics under cold stress, as revealed by footprint analysis. Overexpression of Stat1 in immune cells leads to apoptosis and increases the expression of apoptosis-related genes, many of which contain Stat1-binding sites in their regulatory regions, emphasizing its critical role in immune cell survival during cold stress. These results provide insights into the transcriptional and epigenetic regulation of immune responses to cold stress in tilapia and highlight Stat1 as a promising target for enhancing cold tolerance in tropical fish species.</p>\",\"PeriodicalId\":54825,\"journal\":{\"name\":\"Journal of Genetics and Genomics\",\"volume\":\" \",\"pages\":\"1046-1057\"},\"PeriodicalIF\":7.9000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Genetics and Genomics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.jgg.2025.01.008\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/21 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Genetics and Genomics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.jgg.2025.01.008","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/21 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

温度波动挑战恒温物种,特别是依赖外部温度进行生理调节的热带鱼。然而,低温胁迫影响这些物种免疫反应的分子机制,特别是与染色质可及性和表观遗传调控有关的分子机制仍然知之甚少。在这项研究中,我们研究了尼罗罗非鱼(Oreochromis niloticus)头部肾脏和胸腺组织在寒冷胁迫下的染色质和转录变化。尼罗罗非鱼是一种具有重要经济价值的热带鱼。通过分析开放染色质区域的顺式调控元件及其相关转录因子(TFs),我们构建了一个全面的调控免疫反应的转录调控网络(TRN),包括DNA损伤诱导的细胞凋亡。我们的分析确定了TRN内的119个tf,正如足迹分析所揭示的那样,Stat1作为中心枢纽在冷应力下表现出明显的结合动力学。Stat1在免疫细胞中的过表达导致细胞凋亡,并增加凋亡相关基因的表达,其中许多基因在其调控区域含有Stat1结合位点,强调其在冷胁迫下免疫细胞存活中的关键作用。这些结果为罗非鱼对冷胁迫免疫反应的转录和表观遗传调控提供了见解,并突出了Stat1作为增强热带鱼物种耐寒性的有希望的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Uncovering the chromatin-mediated transcriptional regulatory network governing cold stress responses in fish immune cells.

Temperature fluctuations challenge ectothermic species, particularly tropical fish dependent on external temperatures for physiological regulation. However, the molecular mechanisms through which low-temperature stress impacts immune responses in these species, especially in relation to chromatin accessibility and epigenetic regulation, remain poorly understood. In this study, we investigate chromatin and transcriptional changes in the head kidney and thymus tissues of Nile tilapia (Oreochromis niloticus), a tropical fish of significant economic importance, under cold stress. By analyzing cis-regulatory elements in open chromatin regions and their associated transcription factors (TFs), we construct a comprehensive transcriptional regulatory network (TRN) governing immune responses, including DNA damage-induced apoptosis. Our analysis identifies 119 TFs within the TRN, with Stat1 emerging as a central hub exhibiting distinct binding dynamics under cold stress, as revealed by footprint analysis. Overexpression of Stat1 in immune cells leads to apoptosis and increases the expression of apoptosis-related genes, many of which contain Stat1-binding sites in their regulatory regions, emphasizing its critical role in immune cell survival during cold stress. These results provide insights into the transcriptional and epigenetic regulation of immune responses to cold stress in tilapia and highlight Stat1 as a promising target for enhancing cold tolerance in tropical fish species.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Genetics and Genomics
Journal of Genetics and Genomics 生物-生化与分子生物学
CiteScore
8.20
自引率
3.40%
发文量
4756
审稿时长
14 days
期刊介绍: The Journal of Genetics and Genomics (JGG, formerly known as Acta Genetica Sinica ) is an international journal publishing peer-reviewed articles of novel and significant discoveries in the fields of genetics and genomics. Topics of particular interest include but are not limited to molecular genetics, developmental genetics, cytogenetics, epigenetics, medical genetics, population and evolutionary genetics, genomics and functional genomics as well as bioinformatics and computational biology.
期刊最新文献
Tapt1 deficiency in mice impairs pulmonary lipid homeostasis and normal postnatal respiration by targeting ABCA3 for autophagy-lysosomal degradation. Polyploidy-induced epigenetic priming underlies enhanced salinity tolerance in soybean. Lipid metabolism and metabolites: emerging roles in systemic physiology and metabolic diseases. Transcriptional, epigenetic, and post-translational regulation of plant autophagy. The ARHGAP10-202aa protein encoded by circARHGAP10 promotes skeletal muscle development and regeneration.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1