The Nuclear and Mitochondrial Genomes ofAmoebophryasp. exKarlodinium veneficum

Author:

DeMontigny Wesley,Bachvaroff TsvetanORCID

Abstract

AbstractDinoflagellates are a diverse group of microplankton that include free-living, symbiotic, and parasitic species.Amoebophrya, a basal lineage of parasitic dinoflagellates, infects a variety of marine microorganisms, including harmful-bloom-forming algae. Although there are currently three publishedAmoebophryagenomes, this genus has considerable genomic diversity. We add to the growing genomic data forAmoebophryawith an annotated genome assembly forAmoebophryasp. exKarlodinium veneficum. This species appears to translate all three canonical stop codons contextually. Stop codons are present in the open reading frames of about half of the predicted gene models, including genes essential for cellular function. The in-frame stop codons are likely translated by suppressor tRNAs that were identified in the assembly. We also assembled the mitochondrial genome, which has remained elusive in the previousAmoebophryagenome assemblies. The mitochondrial genome assembly consists of many fragments with high sequence identity in the genes but low sequence identity in intergenic regions. Nuclear and mitochondrially-encoded proteins indicate thatAmoebophryasp. exK. veneficumdoes not have a bipartite electron transport chain, unlike previously analyzedAmoebophryaspecies. This study highlights the importance of analyzing multiple genomes from highly diverse genera such asAmoebophrya.SummaryThis new long-read assembly demonstrates the remarkable diversity found withinAmoebophrya. Despite being assigned the rank of genus, the available genome assemblies indicate significant variation in gene content, AT content, genetic codes, and potentially mitochondrial biology. Furthermore, this study contributes to the expanding list of organisms that contextually translate all three canonical stop codons. Although the mechanisms underlying such a genetic code remain elusive, the relative ease of culturingAmoebophryasuggests it may be useful as a model organism for future research on this subject.

Publisher

Cold Spring Harbor Laboratory

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3