Maricel Podio, Danilo Fabrizio Santoro, Carolina Marta Colono, Juan Pablo A Ortiz, Emidio Albertini, Silvina Claudia Pessino
{"title":"Leaf transcriptome differences between diploid and tetraploid bahiagrass.","authors":"Maricel Podio, Danilo Fabrizio Santoro, Carolina Marta Colono, Juan Pablo A Ortiz, Emidio Albertini, Silvina Claudia Pessino","doi":"10.1002/tpg2.70212","DOIUrl":null,"url":null,"abstract":"<p><p>Polyploid individuals of the subtropical forage grass Paspalum notatum Flüggé (bahiagrass) exhibit distinct phenotypes, including apomixis, enhanced vigor, gigas effects, and increased stress tolerance. While apomixis-based breeding programs supported by molecular tools have improved agronomic traits such as growth habit, forage dry matter, and lipid profile, a genome-wide understanding of ploidy-induced transcriptomic changes is still lacking. In this study, we aimed to generate a comprehensive reference catalog of transcripts differentially expressed in the leaves of diploid and tetraploid individuals, characterize genome responses to polyploidy, and identify candidate genes for breeding. Our results reveal distinct transcriptomic profiles in polyploids, with significant impacts on development, redox homeostasis, and photosynthesis-patterns consistent with those observed in other species. Gene ontology enrichment analyses highlighted key categories related to stress responses and signaling pathways. We also identified critical breeding targets, including transcription factors and hormone-related genes. Co-expression network analysis uncovered 532 master regulators affected by genome doubling, with non-random distribution across the genome and hotspot clustering in specific chromosomes. Overall, our findings provide novel insights into the molecular consequences of polyploidy in P. notatum, offering a valuable resource for molecular breeding programs aimed at improving stress tolerance, vigor, and other desirable traits.</p>","PeriodicalId":49002,"journal":{"name":"Plant Genome","volume":"19 1","pages":"e70212"},"PeriodicalIF":3.8000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12949672/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Genome","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1002/tpg2.70212","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0
Abstract
Polyploid individuals of the subtropical forage grass Paspalum notatum Flüggé (bahiagrass) exhibit distinct phenotypes, including apomixis, enhanced vigor, gigas effects, and increased stress tolerance. While apomixis-based breeding programs supported by molecular tools have improved agronomic traits such as growth habit, forage dry matter, and lipid profile, a genome-wide understanding of ploidy-induced transcriptomic changes is still lacking. In this study, we aimed to generate a comprehensive reference catalog of transcripts differentially expressed in the leaves of diploid and tetraploid individuals, characterize genome responses to polyploidy, and identify candidate genes for breeding. Our results reveal distinct transcriptomic profiles in polyploids, with significant impacts on development, redox homeostasis, and photosynthesis-patterns consistent with those observed in other species. Gene ontology enrichment analyses highlighted key categories related to stress responses and signaling pathways. We also identified critical breeding targets, including transcription factors and hormone-related genes. Co-expression network analysis uncovered 532 master regulators affected by genome doubling, with non-random distribution across the genome and hotspot clustering in specific chromosomes. Overall, our findings provide novel insights into the molecular consequences of polyploidy in P. notatum, offering a valuable resource for molecular breeding programs aimed at improving stress tolerance, vigor, and other desirable traits.
期刊介绍:
The Plant Genome publishes original research investigating all aspects of plant genomics. Technical breakthroughs reporting improvements in the efficiency and speed of acquiring and interpreting plant genomics data are welcome. The editorial board gives preference to novel reports that use innovative genomic applications that advance our understanding of plant biology that may have applications to crop improvement. The journal also publishes invited review articles and perspectives that offer insight and commentary on recent advances in genomics and their potential for agronomic improvement.