Abir Elguweidi, Melania E Cristescu, Teresa J Crease
{"title":"Effect of copper and nickel exposure on ribosomal DNA variation in Daphnia pulex mutation accumulation lines.","authors":"Abir Elguweidi, Melania E Cristescu, Teresa J Crease","doi":"10.1093/g3journal/jkae305","DOIUrl":null,"url":null,"abstract":"<p><p>The release of heavy metals from industrial, agricultural, and mining activities poses significant risks to aquatic ecosystems by degrading water quality and generating reactive oxygen species (ROS) that can damage DNA in aquatic organisms. Daphnia is a widespread keystone species in freshwater ecosystems that is routinely exposed to a range of anthropogenic and natural stressors. With a fully sequenced genome, a well-understood life history and ecology, and an extensive library of responses to toxicity, Daphnia serves as an ideal model organism for studying the impact of environmental stressors on genomic stability. Ribosomal DNA (rDNA) encodes ribosomal RNA, which is essential for protein synthesis, and the spacers that separate the rRNA genes contain regulatory elements. However, the effects of heavy metals on this region of the genome are not well documented. We used short-read whole-genome sequences to analyze copy number and sequence variation in Daphnia pulex mutation accumulation lines exposed to nickel and copper, both individually and in combination, at concentrations that mimic levels often found at contaminated sites. We found no significant direct effect of chronic exposure to either metal on rDNA copy number or sequence variation. However, the results suggest that nickel and copper exposure may indirectly influence rDNA by altering recombination rates. We also emphasize the importance of interval length between generational samples for accurately assessing the frequency and magnitude of rDNA copy number changes. In addition, we observed differential expansion of rDNA haplotypes, suggesting that they may be clustered within the rDNA array.</p>","PeriodicalId":12468,"journal":{"name":"G3: Genes|Genomes|Genetics","volume":" ","pages":""},"PeriodicalIF":2.1000,"publicationDate":"2024-12-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"G3: Genes|Genomes|Genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/g3journal/jkae305","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
The release of heavy metals from industrial, agricultural, and mining activities poses significant risks to aquatic ecosystems by degrading water quality and generating reactive oxygen species (ROS) that can damage DNA in aquatic organisms. Daphnia is a widespread keystone species in freshwater ecosystems that is routinely exposed to a range of anthropogenic and natural stressors. With a fully sequenced genome, a well-understood life history and ecology, and an extensive library of responses to toxicity, Daphnia serves as an ideal model organism for studying the impact of environmental stressors on genomic stability. Ribosomal DNA (rDNA) encodes ribosomal RNA, which is essential for protein synthesis, and the spacers that separate the rRNA genes contain regulatory elements. However, the effects of heavy metals on this region of the genome are not well documented. We used short-read whole-genome sequences to analyze copy number and sequence variation in Daphnia pulex mutation accumulation lines exposed to nickel and copper, both individually and in combination, at concentrations that mimic levels often found at contaminated sites. We found no significant direct effect of chronic exposure to either metal on rDNA copy number or sequence variation. However, the results suggest that nickel and copper exposure may indirectly influence rDNA by altering recombination rates. We also emphasize the importance of interval length between generational samples for accurately assessing the frequency and magnitude of rDNA copy number changes. In addition, we observed differential expansion of rDNA haplotypes, suggesting that they may be clustered within the rDNA array.
期刊介绍:
G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights.
G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.