{"title":"由雌性瞬态肠道在非摄食的奥斯达克斯幼虫中揭示了预先确定的性别。","authors":"Alice Rouan, Norio Miyamoto, Katrine Worsaae","doi":"10.1186/s13227-025-00251-9","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Within the symbiont-hosting Siboglinidae (Annelida), Osedax stands out as the sole genus capable of degrading bones and displaying pronounced sexual dimorphism (except O. priapus). While macroscopic, gutless females feed on whale falls with their symbiont-housing \"roots\", males are microscopic and non-feeding. Yet, embryos and larvae look identical, and sex is suggested to be environmentally determined, i.e., larvae metamorphose into females on bare bone or into males when finding an adult female.</p><p><strong>Results: </strong>However, we here describe a transient gut present in half of the late larvae and in juvenile females of O. japonicus. We confirm the gut-carrying larvae as being females from sex-specific in situ gene expression. Moreover, morphological evidence coupled with differential gene expression indicate that the 'non-feeding' transient gut may pattern the vascular system and/or act as a gas-exchange surface in juvenile females, before their branchial appendages develop.</p><p><strong>Conclusions: </strong>The transient gut of O. japonicus females reveals a genetic sex determination. Proposedly homologous across siboglinids, this vestigial gut is suggested to function in organ patterning and/or for gas-exchange during development of the gutless adult.</p>","PeriodicalId":49076,"journal":{"name":"Evodevo","volume":"16 1","pages":"15"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12382133/pdf/","citationCount":"0","resultStr":"{\"title\":\"Predetermined sex revealed by a female transient gut in non-feeding larvae of Osedax (Siboglinidae, Annelida).\",\"authors\":\"Alice Rouan, Norio Miyamoto, Katrine Worsaae\",\"doi\":\"10.1186/s13227-025-00251-9\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Within the symbiont-hosting Siboglinidae (Annelida), Osedax stands out as the sole genus capable of degrading bones and displaying pronounced sexual dimorphism (except O. priapus). While macroscopic, gutless females feed on whale falls with their symbiont-housing \\\"roots\\\", males are microscopic and non-feeding. Yet, embryos and larvae look identical, and sex is suggested to be environmentally determined, i.e., larvae metamorphose into females on bare bone or into males when finding an adult female.</p><p><strong>Results: </strong>However, we here describe a transient gut present in half of the late larvae and in juvenile females of O. japonicus. We confirm the gut-carrying larvae as being females from sex-specific in situ gene expression. Moreover, morphological evidence coupled with differential gene expression indicate that the 'non-feeding' transient gut may pattern the vascular system and/or act as a gas-exchange surface in juvenile females, before their branchial appendages develop.</p><p><strong>Conclusions: </strong>The transient gut of O. japonicus females reveals a genetic sex determination. Proposedly homologous across siboglinids, this vestigial gut is suggested to function in organ patterning and/or for gas-exchange during development of the gutless adult.</p>\",\"PeriodicalId\":49076,\"journal\":{\"name\":\"Evodevo\",\"volume\":\"16 1\",\"pages\":\"15\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-08-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12382133/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Evodevo\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1186/s13227-025-00251-9\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DEVELOPMENTAL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Evodevo","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1186/s13227-025-00251-9","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DEVELOPMENTAL BIOLOGY","Score":null,"Total":0}
Predetermined sex revealed by a female transient gut in non-feeding larvae of Osedax (Siboglinidae, Annelida).
Background: Within the symbiont-hosting Siboglinidae (Annelida), Osedax stands out as the sole genus capable of degrading bones and displaying pronounced sexual dimorphism (except O. priapus). While macroscopic, gutless females feed on whale falls with their symbiont-housing "roots", males are microscopic and non-feeding. Yet, embryos and larvae look identical, and sex is suggested to be environmentally determined, i.e., larvae metamorphose into females on bare bone or into males when finding an adult female.
Results: However, we here describe a transient gut present in half of the late larvae and in juvenile females of O. japonicus. We confirm the gut-carrying larvae as being females from sex-specific in situ gene expression. Moreover, morphological evidence coupled with differential gene expression indicate that the 'non-feeding' transient gut may pattern the vascular system and/or act as a gas-exchange surface in juvenile females, before their branchial appendages develop.
Conclusions: The transient gut of O. japonicus females reveals a genetic sex determination. Proposedly homologous across siboglinids, this vestigial gut is suggested to function in organ patterning and/or for gas-exchange during development of the gutless adult.
期刊介绍:
EvoDevo publishes articles on a broad range of topics associated with the translation of genotype to phenotype in a phylogenetic context. Understanding the history of life, the evolution of novelty and the generation of form, whether through embryogenesis, budding, or regeneration are amongst the greatest challenges in biology. We support the understanding of these processes through the many complementary approaches that characterize the field of evo-devo.
The focus of the journal is on research that promotes understanding of the pattern and process of morphological evolution.
All articles that fulfill this aim will be welcome, in particular: evolution of pattern; formation comparative gene function/expression; life history evolution; homology and character evolution; comparative genomics; phylogenetics and palaeontology