A miRNA-mediated gene regulatory network supports seasonal plasticity in the temperate coral Astrangia poculata.

IF 3 2区 生物学 Q2 BIOLOGY
Jill Ashey, Chloé Gilligan, Hollie M Putnam
{"title":"A miRNA-mediated gene regulatory network supports seasonal plasticity in the temperate coral Astrangia poculata.","authors":"Jill Ashey, Chloé Gilligan, Hollie M Putnam","doi":"10.1242/jeb.253001","DOIUrl":null,"url":null,"abstract":"<p><p>Phenotypic plasticity is critical for sessile marine invertebrates facing intensifying climate change. MicroRNAs (miRNAs)-small non-coding RNAs that regulate gene expression-are compelling candidates for mediating such plasticity, but their role in coral biology remains poorly characterized. We used the temperate coral Astrangia poculata, which endures annual temperature ranges exceeding 25°C, to investigate miRNA-mediated plasticity across seasonal and thermal contexts. Adult aposymbiotic colonies were exposed to ambient seasonal temperatures (∼5-22°C) and a chronic +3°C warming treatment from February to August 2021. Monthly physiological sampling showed that seasonal temperature variation drove significant shifts in photosynthesis, respiration, and soluble protein, whereas the +3°C treatment had minimal physiological effect. RNA-seq across three time points (February, June, and August) revealed that seasonal temperature variation also drove the strongest molecular response. Transcriptional functional enrichment shifted from winter protein homeostasis and cellular integrity to summer immunity, metabolism, and reproduction. We also identified 51 A. poculata miRNAs (46 novel), providing the first characterization of the miRNA repertoire in this species. Target prediction and co-expression analyses revealed that while mRNA-miRNA networks appear to maintain a stable infrastructure across seasons and treatments, specific interactions may be rewired to drive seasonal biology. This dynamic regulation is associated with putative suppression of energy-intensive cell division and morphogenesis during winter quiescence, while shifting to regulate tissue remodeling and reproduction genes during the summer. These results establish miRNAs as seasonal gene regulators in a temperate coral and suggest that the molecular infrastructure underlying its plasticity may also confer resilience to moderate thermal stress.</p>","PeriodicalId":15786,"journal":{"name":"Journal of Experimental Biology","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2026-09-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Experimental Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1242/jeb.253001","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Phenotypic plasticity is critical for sessile marine invertebrates facing intensifying climate change. MicroRNAs (miRNAs)-small non-coding RNAs that regulate gene expression-are compelling candidates for mediating such plasticity, but their role in coral biology remains poorly characterized. We used the temperate coral Astrangia poculata, which endures annual temperature ranges exceeding 25°C, to investigate miRNA-mediated plasticity across seasonal and thermal contexts. Adult aposymbiotic colonies were exposed to ambient seasonal temperatures (∼5-22°C) and a chronic +3°C warming treatment from February to August 2021. Monthly physiological sampling showed that seasonal temperature variation drove significant shifts in photosynthesis, respiration, and soluble protein, whereas the +3°C treatment had minimal physiological effect. RNA-seq across three time points (February, June, and August) revealed that seasonal temperature variation also drove the strongest molecular response. Transcriptional functional enrichment shifted from winter protein homeostasis and cellular integrity to summer immunity, metabolism, and reproduction. We also identified 51 A. poculata miRNAs (46 novel), providing the first characterization of the miRNA repertoire in this species. Target prediction and co-expression analyses revealed that while mRNA-miRNA networks appear to maintain a stable infrastructure across seasons and treatments, specific interactions may be rewired to drive seasonal biology. This dynamic regulation is associated with putative suppression of energy-intensive cell division and morphogenesis during winter quiescence, while shifting to regulate tissue remodeling and reproduction genes during the summer. These results establish miRNAs as seasonal gene regulators in a temperate coral and suggest that the molecular infrastructure underlying its plasticity may also confer resilience to moderate thermal stress.

mirna介导的基因调控网络支持温带珊瑚的季节性可塑性。
在气候变化加剧的情况下,无根海洋无脊椎动物的表型可塑性至关重要。MicroRNAs (miRNAs)——调节基因表达的小非编码rna——是介导这种可塑性的令人信服的候选者,但它们在珊瑚生物学中的作用仍然知之甚少。我们使用年温度范围超过25°C的温带珊瑚asstrangia populata来研究mirna介导的季节性和热环境下的可塑性。成年反共生菌落于2021年2月至8月暴露于环境季节性温度(~ 5-22°C)和慢性+3°C加热处理。月度生理采样显示,季节温度变化导致光合作用、呼吸作用和可溶性蛋白发生显著变化,而+3℃处理对生理影响最小。3个时间点(2月、6月和8月)的RNA-seq显示,季节性温度变化也驱动了最强的分子反应。转录功能的富集从冬季蛋白质稳态和细胞完整性转移到夏季免疫、代谢和生殖。我们还鉴定了51种A. poculata miRNA(46种新发现的miRNA),首次对该物种的miRNA库进行了表征。靶标预测和共表达分析显示,尽管mRNA-miRNA网络似乎在不同季节和治疗中保持稳定的基础结构,但特定的相互作用可能会重新连接以驱动季节性生物学。这种动态调节被认为与冬季静止期间能量密集型细胞分裂和形态发生的抑制有关,而在夏季转移到调节组织重塑和生殖基因。这些结果确定了mirna在温带珊瑚中作为季节性基因调节因子,并表明其可塑性背后的分子基础结构也可能赋予其对适度热应力的弹性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
5.50
自引率
10.70%
发文量
494
审稿时长
1 months
期刊介绍: Journal of Experimental Biology is the leading primary research journal in comparative physiology and publishes papers on the form and function of living organisms at all levels of biological organisation, from the molecular and subcellular to the integrated whole animal.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书