Angela K. Jiang , Taylor R. Sehein , Rebecca Gawron , Laura A. Katz , Xyrus X. Maurer-Alcalá
{"title":"雄性叶状变形虫(Arcellinida)谱系特异性基因的研究","authors":"Angela K. Jiang , Taylor R. Sehein , Rebecca Gawron , Laura A. Katz , Xyrus X. Maurer-Alcalá","doi":"10.1016/j.protis.2025.126115","DOIUrl":null,"url":null,"abstract":"<div><div>Arcellinida are an abundant and diverse order of testate (shelled) amoebae that are important bioindicators of changing climates. Despite their ecological importance, the molecular mechanisms that underlie their adaptations, including those involving lineage-specific genes, remain largely unknown. Lineage-specific gene families (LSGFs) are linked to evolutionary innovations, yet the evolution of LSGFs remains underexplored across the tree of life, with most research restricted to model eukaryotes. Here, we assess the evolution of Arcellinida-specific gene families using a set of 197 Arcellinida transcriptomes representing 12 Arcellinida genera. We employ a conservative filtering approach to identify 3424 Arcellinda-specific gene families. Our analyses show that these lineage-specific gene families are shorter and exhibit lower expression compared to more conserved genes, congruent with trends observed in other eukaryotic lineages. Although there are inherent limitations regarding missing data with transcriptomics, we recover substantially more lineage-specific gene family births in the symbiont-bearing species <em>Hyalosphenia papilio</em> compared to <em>Hyalosphenia elegans</em>. Our results demonstrate a method to identify lineage-specific genes in non-model organisms where no reference genome are available, and expand our understanding of the evolution of lineage-specific genes in eukaryotes.</div></div>","PeriodicalId":20781,"journal":{"name":"Protist","volume":"178 ","pages":"Article 126115"},"PeriodicalIF":2.1000,"publicationDate":"2025-08-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Characterizing lineage-specific genes in testate lobose amoebae (Arcellinida)\",\"authors\":\"Angela K. Jiang , Taylor R. Sehein , Rebecca Gawron , Laura A. Katz , Xyrus X. Maurer-Alcalá\",\"doi\":\"10.1016/j.protis.2025.126115\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Arcellinida are an abundant and diverse order of testate (shelled) amoebae that are important bioindicators of changing climates. Despite their ecological importance, the molecular mechanisms that underlie their adaptations, including those involving lineage-specific genes, remain largely unknown. Lineage-specific gene families (LSGFs) are linked to evolutionary innovations, yet the evolution of LSGFs remains underexplored across the tree of life, with most research restricted to model eukaryotes. Here, we assess the evolution of Arcellinida-specific gene families using a set of 197 Arcellinida transcriptomes representing 12 Arcellinida genera. We employ a conservative filtering approach to identify 3424 Arcellinda-specific gene families. Our analyses show that these lineage-specific gene families are shorter and exhibit lower expression compared to more conserved genes, congruent with trends observed in other eukaryotic lineages. Although there are inherent limitations regarding missing data with transcriptomics, we recover substantially more lineage-specific gene family births in the symbiont-bearing species <em>Hyalosphenia papilio</em> compared to <em>Hyalosphenia elegans</em>. Our results demonstrate a method to identify lineage-specific genes in non-model organisms where no reference genome are available, and expand our understanding of the evolution of lineage-specific genes in eukaryotes.</div></div>\",\"PeriodicalId\":20781,\"journal\":{\"name\":\"Protist\",\"volume\":\"178 \",\"pages\":\"Article 126115\"},\"PeriodicalIF\":2.1000,\"publicationDate\":\"2025-08-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Protist\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1434461025000318\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Protist","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1434461025000318","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Characterizing lineage-specific genes in testate lobose amoebae (Arcellinida)
Arcellinida are an abundant and diverse order of testate (shelled) amoebae that are important bioindicators of changing climates. Despite their ecological importance, the molecular mechanisms that underlie their adaptations, including those involving lineage-specific genes, remain largely unknown. Lineage-specific gene families (LSGFs) are linked to evolutionary innovations, yet the evolution of LSGFs remains underexplored across the tree of life, with most research restricted to model eukaryotes. Here, we assess the evolution of Arcellinida-specific gene families using a set of 197 Arcellinida transcriptomes representing 12 Arcellinida genera. We employ a conservative filtering approach to identify 3424 Arcellinda-specific gene families. Our analyses show that these lineage-specific gene families are shorter and exhibit lower expression compared to more conserved genes, congruent with trends observed in other eukaryotic lineages. Although there are inherent limitations regarding missing data with transcriptomics, we recover substantially more lineage-specific gene family births in the symbiont-bearing species Hyalosphenia papilio compared to Hyalosphenia elegans. Our results demonstrate a method to identify lineage-specific genes in non-model organisms where no reference genome are available, and expand our understanding of the evolution of lineage-specific genes in eukaryotes.
期刊介绍:
Protist is the international forum for reporting substantial and novel findings in any area of research on protists. The criteria for acceptance of manuscripts are scientific excellence, significance, and interest for a broad readership. Suitable subject areas include: molecular, cell and developmental biology, biochemistry, systematics and phylogeny, and ecology of protists. Both autotrophic and heterotrophic protists as well as parasites are covered. The journal publishes original papers, short historical perspectives and includes a news and views section.