Matthew Beaumont, Divya Selvaraju, Riccardo Pianezza, Robert Kofler
{"title":"在缺乏基于pirna的宿主防御的情况下,非自主元素的迅速出现可能会阻止p元素的入侵。","authors":"Matthew Beaumont, Divya Selvaraju, Riccardo Pianezza, Robert Kofler","doi":"10.1371/journal.pgen.1011649","DOIUrl":null,"url":null,"abstract":"<p><p>Transposable element (TE) invasions pose risks to both the TE and the host. All copies of a TE may be lost via genetic drift, or host populations may suffer fitness declines, potentially leading to extinction. By monitoring invasions of the P-element in experimental D. melanogaster populations for over 100 generations, we uncovered a novel risk for invading TEs. In two replicate populations, the P-element rapidly multiplied until a piRNA-based host defence emerged, leading to the plateauing of TE copy numbers. However, in one population (R2), P-element copy numbers stabilised at a significantly lower level, despite the absence of a piRNA-based host defence. We find that this stabilisation was likely driven by the propagation of non-autonomous insertions, characterised by internal-deletions, which out-competed the autonomous full-length insertions. Such a rapid proliferation of non-autonomous insertions could account for the high prevalence of P-element insertions with internal-deletions observed in natural D. melanogaster populations. Our work reveals that TEs may stochastically sabotage their own spread in populations due to the emergence of non-autonomous elements, rendering the establishment of a host defence unnecessary. The proliferation of non-autonomous elements may also lead into an evolutionary dead end, where affected populations are resistant to re-invasion (e.g. following recurrent horizontal transfer), yet are unable to infect other species due to a lack of autonomous insertions.</p>","PeriodicalId":49007,"journal":{"name":"PLoS Genetics","volume":"21 8","pages":"e1011649"},"PeriodicalIF":3.7000,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12393704/pdf/","citationCount":"0","resultStr":"{\"title\":\"Rapid emergence of non-autonomous elements may stop P-element invasions in the absence of a piRNA-based host defence.\",\"authors\":\"Matthew Beaumont, Divya Selvaraju, Riccardo Pianezza, Robert Kofler\",\"doi\":\"10.1371/journal.pgen.1011649\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Transposable element (TE) invasions pose risks to both the TE and the host. All copies of a TE may be lost via genetic drift, or host populations may suffer fitness declines, potentially leading to extinction. By monitoring invasions of the P-element in experimental D. melanogaster populations for over 100 generations, we uncovered a novel risk for invading TEs. In two replicate populations, the P-element rapidly multiplied until a piRNA-based host defence emerged, leading to the plateauing of TE copy numbers. However, in one population (R2), P-element copy numbers stabilised at a significantly lower level, despite the absence of a piRNA-based host defence. We find that this stabilisation was likely driven by the propagation of non-autonomous insertions, characterised by internal-deletions, which out-competed the autonomous full-length insertions. Such a rapid proliferation of non-autonomous insertions could account for the high prevalence of P-element insertions with internal-deletions observed in natural D. melanogaster populations. Our work reveals that TEs may stochastically sabotage their own spread in populations due to the emergence of non-autonomous elements, rendering the establishment of a host defence unnecessary. The proliferation of non-autonomous elements may also lead into an evolutionary dead end, where affected populations are resistant to re-invasion (e.g. following recurrent horizontal transfer), yet are unable to infect other species due to a lack of autonomous insertions.</p>\",\"PeriodicalId\":49007,\"journal\":{\"name\":\"PLoS Genetics\",\"volume\":\"21 8\",\"pages\":\"e1011649\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-08-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12393704/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"PLoS Genetics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1371/journal.pgen.1011649\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q1\",\"JCRName\":\"GENETICS & HEREDITY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"PLoS Genetics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1371/journal.pgen.1011649","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
Rapid emergence of non-autonomous elements may stop P-element invasions in the absence of a piRNA-based host defence.
Transposable element (TE) invasions pose risks to both the TE and the host. All copies of a TE may be lost via genetic drift, or host populations may suffer fitness declines, potentially leading to extinction. By monitoring invasions of the P-element in experimental D. melanogaster populations for over 100 generations, we uncovered a novel risk for invading TEs. In two replicate populations, the P-element rapidly multiplied until a piRNA-based host defence emerged, leading to the plateauing of TE copy numbers. However, in one population (R2), P-element copy numbers stabilised at a significantly lower level, despite the absence of a piRNA-based host defence. We find that this stabilisation was likely driven by the propagation of non-autonomous insertions, characterised by internal-deletions, which out-competed the autonomous full-length insertions. Such a rapid proliferation of non-autonomous insertions could account for the high prevalence of P-element insertions with internal-deletions observed in natural D. melanogaster populations. Our work reveals that TEs may stochastically sabotage their own spread in populations due to the emergence of non-autonomous elements, rendering the establishment of a host defence unnecessary. The proliferation of non-autonomous elements may also lead into an evolutionary dead end, where affected populations are resistant to re-invasion (e.g. following recurrent horizontal transfer), yet are unable to infect other species due to a lack of autonomous insertions.
期刊介绍:
PLOS Genetics is run by an international Editorial Board, headed by the Editors-in-Chief, Greg Barsh (HudsonAlpha Institute of Biotechnology, and Stanford University School of Medicine) and Greg Copenhaver (The University of North Carolina at Chapel Hill).
Articles published in PLOS Genetics are archived in PubMed Central and cited in PubMed.