Nikita Jhaveri, Harvir Bhullar, Paul W Sternberg, Bhagwati P Gupta
{"title":"布氏拟尾线虫的耐热性和遗传适应性:与秀丽隐杆线虫比较研究的启示》(Caenorhabditis briggsae: Insights from Comparative Studies with C. elegans)。","authors":"Nikita Jhaveri, Harvir Bhullar, Paul W Sternberg, Bhagwati P Gupta","doi":"10.1093/genetics/iyaf061","DOIUrl":null,"url":null,"abstract":"<p><p>Temperature tolerance varies widely across species and plays a crucial role in shaping physiological and evolutionary adaptations. Here, we investigate thermal stress responses in Caenorhabditis briggsae and Caenorhabditis elegans using multiple isolates. Our results demonstrate that C. briggsae exhibits enhanced survival, growth, and reproduction at elevated temperatures compared to C. elegans. The increased heat resistance was evident from the L1 larval stage. Notably, C. briggsae isolates from both tropical and temperate regions were equally resistant to heat stress, suggesting that elevated thermal tolerance is an intrinsic feature of this species. To explore the molecular genetic basis of thermal tolerance, we examined expression of heat shock regulators. Transcriptional analysis revealed that C. briggsae mounts a rapid and robust heat shock response, with CBG19186, the closest ortholog of C. eleganshsp-16.2, showing higher induction and faster recovery dynamics. The peak expression of hsp-16.2/CBG19186 occurred at a temperature 2°C higher in C. briggsae than in C. elegans. These findings provide the first in vivo evidence of temperature differences in the transcriptional response of a single protein between the 2 species, suggesting that C. briggsae has evolved a higher thermal limit for key molecular processes, likely contributing to its ability to withstand extreme temperatures. Despite its superior thermal resistance, C. briggsae showed higher sensitivity to oxidative, osmotic, and endoplasmic reticulum stress, suggesting a potential fitness trade-off. Our findings demonstrate significant differences in stress sensitivities between the 2 nematodes, providing a foundation for further investigations into the molecular and evolutionary mechanisms underlying their stress responses.</p>","PeriodicalId":48925,"journal":{"name":"Genetics","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-06-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12135185/pdf/","citationCount":"0","resultStr":"{\"title\":\"Heat tolerance and genetic adaptations in Caenorhabditis briggsae: insights from comparative studies with Caenorhabditis elegans.\",\"authors\":\"Nikita Jhaveri, Harvir Bhullar, Paul W Sternberg, Bhagwati P Gupta\",\"doi\":\"10.1093/genetics/iyaf061\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Temperature tolerance varies widely across species and plays a crucial role in shaping physiological and evolutionary adaptations. Here, we investigate thermal stress responses in Caenorhabditis briggsae and Caenorhabditis elegans using multiple isolates. Our results demonstrate that C. briggsae exhibits enhanced survival, growth, and reproduction at elevated temperatures compared to C. elegans. The increased heat resistance was evident from the L1 larval stage. Notably, C. briggsae isolates from both tropical and temperate regions were equally resistant to heat stress, suggesting that elevated thermal tolerance is an intrinsic feature of this species. To explore the molecular genetic basis of thermal tolerance, we examined expression of heat shock regulators. Transcriptional analysis revealed that C. briggsae mounts a rapid and robust heat shock response, with CBG19186, the closest ortholog of C. eleganshsp-16.2, showing higher induction and faster recovery dynamics. The peak expression of hsp-16.2/CBG19186 occurred at a temperature 2°C higher in C. briggsae than in C. elegans. These findings provide the first in vivo evidence of temperature differences in the transcriptional response of a single protein between the 2 species, suggesting that C. briggsae has evolved a higher thermal limit for key molecular processes, likely contributing to its ability to withstand extreme temperatures. Despite its superior thermal resistance, C. briggsae showed higher sensitivity to oxidative, osmotic, and endoplasmic reticulum stress, suggesting a potential fitness trade-off. Our findings demonstrate significant differences in stress sensitivities between the 2 nematodes, providing a foundation for further investigations into the molecular and evolutionary mechanisms underlying their stress responses.</p>\",\"PeriodicalId\":48925,\"journal\":{\"name\":\"Genetics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-06-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12135185/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genetics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/genetics/iyaf061\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/genetics/iyaf061","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Heat tolerance and genetic adaptations in Caenorhabditis briggsae: insights from comparative studies with Caenorhabditis elegans.
Temperature tolerance varies widely across species and plays a crucial role in shaping physiological and evolutionary adaptations. Here, we investigate thermal stress responses in Caenorhabditis briggsae and Caenorhabditis elegans using multiple isolates. Our results demonstrate that C. briggsae exhibits enhanced survival, growth, and reproduction at elevated temperatures compared to C. elegans. The increased heat resistance was evident from the L1 larval stage. Notably, C. briggsae isolates from both tropical and temperate regions were equally resistant to heat stress, suggesting that elevated thermal tolerance is an intrinsic feature of this species. To explore the molecular genetic basis of thermal tolerance, we examined expression of heat shock regulators. Transcriptional analysis revealed that C. briggsae mounts a rapid and robust heat shock response, with CBG19186, the closest ortholog of C. eleganshsp-16.2, showing higher induction and faster recovery dynamics. The peak expression of hsp-16.2/CBG19186 occurred at a temperature 2°C higher in C. briggsae than in C. elegans. These findings provide the first in vivo evidence of temperature differences in the transcriptional response of a single protein between the 2 species, suggesting that C. briggsae has evolved a higher thermal limit for key molecular processes, likely contributing to its ability to withstand extreme temperatures. Despite its superior thermal resistance, C. briggsae showed higher sensitivity to oxidative, osmotic, and endoplasmic reticulum stress, suggesting a potential fitness trade-off. Our findings demonstrate significant differences in stress sensitivities between the 2 nematodes, providing a foundation for further investigations into the molecular and evolutionary mechanisms underlying their stress responses.
期刊介绍:
GENETICS is published by the Genetics Society of America, a scholarly society that seeks to deepen our understanding of the living world by advancing our understanding of genetics. Since 1916, GENETICS has published high-quality, original research presenting novel findings bearing on genetics and genomics. The journal publishes empirical studies of organisms ranging from microbes to humans, as well as theoretical work.
While it has an illustrious history, GENETICS has changed along with the communities it serves: it is not your mentor''s journal.
The editors make decisions quickly – in around 30 days – without sacrificing the excellence and scholarship for which the journal has long been known. GENETICS is a peer reviewed, peer-edited journal, with an international reach and increasing visibility and impact. All editorial decisions are made through collaboration of at least two editors who are practicing scientists.
GENETICS is constantly innovating: expanded types of content include Reviews, Commentary (current issues of interest to geneticists), Perspectives (historical), Primers (to introduce primary literature into the classroom), Toolbox Reviews, plus YeastBook, FlyBook, and WormBook (coming spring 2016). For particularly time-sensitive results, we publish Communications. As part of our mission to serve our communities, we''ve published thematic collections, including Genomic Selection, Multiparental Populations, Mouse Collaborative Cross, and the Genetics of Sex.