Ostermayer Jasmin , Guzzi Noa , Czarnecki Jakub , Soler-Bistué Alfonso , Mazel Didier , Val Marie-Eve
{"title":"驯化野生复制子:进化和驯化大型染色体外复制子","authors":"Ostermayer Jasmin , Guzzi Noa , Czarnecki Jakub , Soler-Bistué Alfonso , Mazel Didier , Val Marie-Eve","doi":"10.1016/j.mib.2025.102657","DOIUrl":null,"url":null,"abstract":"<div><div>Bacterial genomes often contain extrachromosomal replicons (ERs), ranging from small, mobile plasmids to large, stably inherited elements, such as megaplasmids, secondary chromosomes, or chromids. Multipartite genomes, which include large ERs, are present in approximately 10% of sequenced bacterial species and are thought to have evolved as adaptive solutions to diverse ecological niches. Understanding how these replicons become essential genome components is critical for characterizing bacterial adaptability and genome plasticity. Large ERs become established within the host genome through evolutionary processes that shape their genetic content, promote the acquisition of core functions, and synchronize their replication and segregation with the bacterial cell cycle. In this review, we examine the origin, classification, and functional roles of large ERs. We highlight shared maintenance principles, such as dosage-dependent gene organization, replication control via methylation or checkpoint mechanisms, and dedicated partitioning systems or shared segregation machinery. Examples from <em>Vibrio cholerae</em> and <em>Agrobacterium tumefaciens</em> illustrate these mechanisms, and a conceptual model for ER domestication is proposed.</div></div>","PeriodicalId":10921,"journal":{"name":"Current opinion in microbiology","volume":"88 ","pages":"Article 102657"},"PeriodicalIF":7.5000,"publicationDate":"2025-08-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Taming wild replicons: evolution and domestication of large extrachromosomal replicons\",\"authors\":\"Ostermayer Jasmin , Guzzi Noa , Czarnecki Jakub , Soler-Bistué Alfonso , Mazel Didier , Val Marie-Eve\",\"doi\":\"10.1016/j.mib.2025.102657\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Bacterial genomes often contain extrachromosomal replicons (ERs), ranging from small, mobile plasmids to large, stably inherited elements, such as megaplasmids, secondary chromosomes, or chromids. Multipartite genomes, which include large ERs, are present in approximately 10% of sequenced bacterial species and are thought to have evolved as adaptive solutions to diverse ecological niches. Understanding how these replicons become essential genome components is critical for characterizing bacterial adaptability and genome plasticity. Large ERs become established within the host genome through evolutionary processes that shape their genetic content, promote the acquisition of core functions, and synchronize their replication and segregation with the bacterial cell cycle. In this review, we examine the origin, classification, and functional roles of large ERs. We highlight shared maintenance principles, such as dosage-dependent gene organization, replication control via methylation or checkpoint mechanisms, and dedicated partitioning systems or shared segregation machinery. Examples from <em>Vibrio cholerae</em> and <em>Agrobacterium tumefaciens</em> illustrate these mechanisms, and a conceptual model for ER domestication is proposed.</div></div>\",\"PeriodicalId\":10921,\"journal\":{\"name\":\"Current opinion in microbiology\",\"volume\":\"88 \",\"pages\":\"Article 102657\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2025-08-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current opinion in microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1369527425000797\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current opinion in microbiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1369527425000797","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Taming wild replicons: evolution and domestication of large extrachromosomal replicons
Bacterial genomes often contain extrachromosomal replicons (ERs), ranging from small, mobile plasmids to large, stably inherited elements, such as megaplasmids, secondary chromosomes, or chromids. Multipartite genomes, which include large ERs, are present in approximately 10% of sequenced bacterial species and are thought to have evolved as adaptive solutions to diverse ecological niches. Understanding how these replicons become essential genome components is critical for characterizing bacterial adaptability and genome plasticity. Large ERs become established within the host genome through evolutionary processes that shape their genetic content, promote the acquisition of core functions, and synchronize their replication and segregation with the bacterial cell cycle. In this review, we examine the origin, classification, and functional roles of large ERs. We highlight shared maintenance principles, such as dosage-dependent gene organization, replication control via methylation or checkpoint mechanisms, and dedicated partitioning systems or shared segregation machinery. Examples from Vibrio cholerae and Agrobacterium tumefaciens illustrate these mechanisms, and a conceptual model for ER domestication is proposed.
期刊介绍:
Current Opinion in Microbiology is a systematic review journal that aims to provide specialists with a unique and educational platform to keep up-to-date with the expanding volume of information published in the field of microbiology. It consists of 6 issues per year covering the following 11 sections, each of which is reviewed once a year:
Host-microbe interactions: bacteria
Cell regulation
Environmental microbiology
Host-microbe interactions: fungi/parasites/viruses
Antimicrobials
Microbial systems biology
Growth and development: eukaryotes/prokaryotes