{"title":"Loss of the starvation-and-light fruitbody formation trigger in the myxomycete <i>Physarum roseum</i>.","authors":"Mana Masui, Phillip K Yamamoto, Nobuaki Kono","doi":"10.1098/rsbl.2025.0215","DOIUrl":null,"url":null,"abstract":"<p><p>Myxomycetes are unicellular amoebozoans that form fruiting bodies to reproduce, a process known as sporulation. In the model species <i>Physarum polycephalum</i>, plasmodia form fruiting bodies only after several days of starvation followed by light exposure. It has long been assumed that the same starvation-plus-light trigger applies to the genus <i>Physarum</i>. Recent observations of congeners that fail to sporulate under the same conditions have raised doubts about this assumption and prompted tentative taxonomic reconsideration. Because comparable starvation and light tests are rare for other species of <i>Physarum</i>, their phenotypes and molecular mechanisms remain unclear. Consequently, we investigated <i>Physarum rigidum</i> and <i>Physarum roseum</i> under starvation and light conditions. Four of the six <i>P. rigidum</i> plasmodia sporulated by day 6, whereas <i>P. roseum</i> did not sporulate within 7 days. RNA-seq of <i>P. roseum</i> across nutrient-rich/starved and dark/light conditions revealed differential expression was driven chiefly by nutrition; light caused only minor changes and did not elicit the transcriptional programme characteristic of <i>P. polycephalum</i> sporulation. The photoreceptor genes that drive sporulation in <i>P. polycephalum</i> were not detected in <i>P. roseum</i>, and 92 candidate photoreceptor genes showed no significant regulation. These findings suggest that <i>P. roseum</i> responds only minimally to light stimulation and that the starvation-plus-light trigger is not universally retained within the genus <i>Physarum</i>.</p>","PeriodicalId":9005,"journal":{"name":"Biology Letters","volume":"21 7","pages":"20250215"},"PeriodicalIF":3.0000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12308756/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biology Letters","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1098/rsbl.2025.0215","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/30 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Myxomycetes are unicellular amoebozoans that form fruiting bodies to reproduce, a process known as sporulation. In the model species Physarum polycephalum, plasmodia form fruiting bodies only after several days of starvation followed by light exposure. It has long been assumed that the same starvation-plus-light trigger applies to the genus Physarum. Recent observations of congeners that fail to sporulate under the same conditions have raised doubts about this assumption and prompted tentative taxonomic reconsideration. Because comparable starvation and light tests are rare for other species of Physarum, their phenotypes and molecular mechanisms remain unclear. Consequently, we investigated Physarum rigidum and Physarum roseum under starvation and light conditions. Four of the six P. rigidum plasmodia sporulated by day 6, whereas P. roseum did not sporulate within 7 days. RNA-seq of P. roseum across nutrient-rich/starved and dark/light conditions revealed differential expression was driven chiefly by nutrition; light caused only minor changes and did not elicit the transcriptional programme characteristic of P. polycephalum sporulation. The photoreceptor genes that drive sporulation in P. polycephalum were not detected in P. roseum, and 92 candidate photoreceptor genes showed no significant regulation. These findings suggest that P. roseum responds only minimally to light stimulation and that the starvation-plus-light trigger is not universally retained within the genus Physarum.
期刊介绍:
Previously a supplement to Proceedings B, and launched as an independent journal in 2005, Biology Letters is a primarily online, peer-reviewed journal that publishes short, high-quality articles, reviews and opinion pieces from across the biological sciences. The scope of Biology Letters is vast - publishing high-quality research in any area of the biological sciences. However, we have particular strengths in the biology, evolution and ecology of whole organisms. We also publish in other areas of biology, such as molecular ecology and evolution, environmental science, and phylogenetics.