Chromosome-level genome provides novel insights into the starch metabolism regulation and evolutionary history of Tetraselmis helgolandica

IF 17.1 1区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES Journal of Advanced Research Pub Date : 2026-01-01 Epub Date: 2025-03-25 DOI:10.1016/j.jare.2025.03.022
Zuodong Zhou , Jiawei E , Qianwen Shi , Wenjun Zhang , Liyun Sun , Jianhua Fan
{"title":"Chromosome-level genome provides novel insights into the starch metabolism regulation and evolutionary history of Tetraselmis helgolandica","authors":"Zuodong Zhou ,&nbsp;Jiawei E ,&nbsp;Qianwen Shi ,&nbsp;Wenjun Zhang ,&nbsp;Liyun Sun ,&nbsp;Jianhua Fan","doi":"10.1016/j.jare.2025.03.022","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div><em>Tetraselmis helgolandica</em> is a marine microalga belonging to the Chlorophyta phylum. It is widely distributed in the coastal waters of Asia and is commonly used as aquatic feed. <em>T. helgolandica</em> is characterized by its large size, preference for starch accumulation, low temperature tolerance, presence of flagella, and strong motility. However, research on <em>T. helgolandica</em> is limited, and its genome data remains unavailable.</div></div><div><h3>Objective</h3><div>We generated a high-quality, chromosome-scale genome of <em>T. helgolandica</em>. Through comparative genomics, we uncovered the genome characteristics and evolutionary history of <em>T. helgolandica</em>. Additionally, by integrating transcriptome data, we elucidated how the light–dark rhythm enhances the high starch production.</div></div><div><h3>Methods</h3><div>We utilized long-read sequencing data and high-throughput chromosome conformation capture data from the Oxford Nanopore platform to construct a high-quality genome of <em>T. helgolandica.</em> Genome annotation was performed using multiple databases, and comparative genomic analysis was conducted with nine species, including <em>Arabidopsis thaliana</em>, to reveal the evolutionary history. Finally, we combined transcriptome data to elucidate the molecular mechanisms underlying the high starch yield.</div></div><div><h3>Results</h3><div>Circadian rhythm significantly promote starch accumulation and increase amylose content. The chromosome-scale genome revealed it shares a common ancestor with other green algae approximately 1,017 million years ago. This relatively ancient divergence underscores its evolutionary distinction within the green lineage. It may possess a more complex protein modification mechanism and a more fully developed Golgi apparatus. Circadian rhythm broadly up-regulates key enzymes involved in starch synthesis, including GBSS and Starch Synthase, while down-regulating SS IIIa. This regulation enhances starch accumulation and increases the amylose content.</div></div><div><h3>Conclusion</h3><div>This study provided a high-quality genome of <em>T. helgolandica</em> and revealed the potential mechanism by which the circadian rhythm promotes starch accumulation and increases the amylose ratio. The genome of <em>T. helgolandica</em> will serve as an important resource for evolutionary research and transgenic platform development.</div></div>","PeriodicalId":14952,"journal":{"name":"Journal of Advanced Research","volume":"79 ","pages":"Pages 251-262"},"PeriodicalIF":17.1000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Research","FirstCategoryId":"103","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2090123225001821","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/25 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Tetraselmis helgolandica is a marine microalga belonging to the Chlorophyta phylum. It is widely distributed in the coastal waters of Asia and is commonly used as aquatic feed. T. helgolandica is characterized by its large size, preference for starch accumulation, low temperature tolerance, presence of flagella, and strong motility. However, research on T. helgolandica is limited, and its genome data remains unavailable.

Objective

We generated a high-quality, chromosome-scale genome of T. helgolandica. Through comparative genomics, we uncovered the genome characteristics and evolutionary history of T. helgolandica. Additionally, by integrating transcriptome data, we elucidated how the light–dark rhythm enhances the high starch production.

Methods

We utilized long-read sequencing data and high-throughput chromosome conformation capture data from the Oxford Nanopore platform to construct a high-quality genome of T. helgolandica. Genome annotation was performed using multiple databases, and comparative genomic analysis was conducted with nine species, including Arabidopsis thaliana, to reveal the evolutionary history. Finally, we combined transcriptome data to elucidate the molecular mechanisms underlying the high starch yield.

Results

Circadian rhythm significantly promote starch accumulation and increase amylose content. The chromosome-scale genome revealed it shares a common ancestor with other green algae approximately 1,017 million years ago. This relatively ancient divergence underscores its evolutionary distinction within the green lineage. It may possess a more complex protein modification mechanism and a more fully developed Golgi apparatus. Circadian rhythm broadly up-regulates key enzymes involved in starch synthesis, including GBSS and Starch Synthase, while down-regulating SS IIIa. This regulation enhances starch accumulation and increases the amylose content.

Conclusion

This study provided a high-quality genome of T. helgolandica and revealed the potential mechanism by which the circadian rhythm promotes starch accumulation and increases the amylose ratio. The genome of T. helgolandica will serve as an important resource for evolutionary research and transgenic platform development.

Abstract Image

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
染色体水平的基因组研究为海芋淀粉代谢调控和进化历史提供了新的见解
四藻是一种海洋微藻,属于绿藻门。它广泛分布在亚洲沿海水域,通常用作水生饲料。其特点是体型大,偏好淀粉积累,耐低温,存在鞭毛,运动性强。然而,对黑胶霉的研究是有限的,其基因组数据仍然不可用。目的制备高质量、高染色体尺度的黑果菌基因组。通过比较基因组学的研究,揭示了黑牙霉的基因组特征和进化史。此外,通过整合转录组数据,我们阐明了明暗节律如何提高高淀粉产量。方法利用牛津纳米孔平台的长读测序数据和高通量染色体构象捕获数据,构建高质量的黑耳菌基因组。利用多个数据库进行基因组注释,并与拟南芥(Arabidopsis thaliana)等9个物种进行比较基因组分析,揭示其进化史。最后,我们结合转录组数据来阐明高淀粉产量的分子机制。结果昼夜节律显著促进淀粉积累,增加直链淀粉含量。染色体规模的基因组显示,大约10.17亿年前,它与其他绿藻拥有共同的祖先。这种相对古老的分化强调了其在绿色谱系中的进化区别。它可能具有更复杂的蛋白质修饰机制和更发达的高尔基体。昼夜节律广泛上调参与淀粉合成的关键酶,包括GBSS和starch Synthase,同时下调SSⅢa。这种调节促进了淀粉的积累,增加了直链淀粉的含量。结论本研究提供了高质量的黑果甘露基因组,揭示了昼夜节律促进淀粉积累和增加直链淀粉比率的潜在机制。其基因组可作为进化研究和转基因平台开发的重要资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Advanced Research
Journal of Advanced Research Multidisciplinary-Multidisciplinary
CiteScore
21.60
自引率
0.90%
发文量
280
审稿时长
12 weeks
期刊介绍: Journal of Advanced Research (J. Adv. Res.) is an applied/natural sciences, peer-reviewed journal that focuses on interdisciplinary research. The journal aims to contribute to applied research and knowledge worldwide through the publication of original and high-quality research articles in the fields of Medicine, Pharmaceutical Sciences, Dentistry, Physical Therapy, Veterinary Medicine, and Basic and Biological Sciences. The following abstracting and indexing services cover the Journal of Advanced Research: PubMed/Medline, Essential Science Indicators, Web of Science, Scopus, PubMed Central, PubMed, Science Citation Index Expanded, Directory of Open Access Journals (DOAJ), and INSPEC.
期刊最新文献
Impact of technological heterogeneity on economic efficiency and total factor productivity change in developed and developing G20 economies Zinc and metformin co-functionalized polyetheretherketone: A novel dental implant material tailored for the elderly Role of Netrin-1 dysregulation in early neuronal pathology of α-synuclein models of Parkinson’s disease Tumour-specific delivery of ω-conotoxin MVIIA via engineered Salmonella for safe anticancer therapy FungiSNC: An integrated database for fungi small non-coding RNAs based on high-throughput sequencing
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1