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法属波利尼西亚产高雪蛤毒素裸甲藻和低毒性太平洋裸甲藻中聚酮合酶的转录组分析。

Transcriptomic analysis of polyketide synthases in a highly ciguatoxic dinoflagellate, Gambierdiscus polynesiensis and low toxicity Gambierdiscus pacificus, from French Polynesia.

机构信息

Marine Genomics Core, Hollings Marine Laboratory, Charleston, SC, United States of America.

Charleston Computational Genomics Group, Department of Computer Science, College of Charleston, Charleston, SC, United States of America.

出版信息

PLoS One. 2020 Apr 15;15(4):e0231400. doi: 10.1371/journal.pone.0231400. eCollection 2020.

Abstract

Marine dinoflagellates produce a diversity of polyketide toxins that are accumulated in marine food webs and are responsible for a variety of seafood poisonings. Reef-associated dinoflagellates of the genus Gambierdiscus produce toxins responsible for ciguatera poisoning (CP), which causes over 50,000 cases of illness annually worldwide. The biosynthetic machinery for dinoflagellate polyketides remains poorly understood. Recent transcriptomic and genomic sequencing projects have revealed the presence of Type I modular polyketide synthases in dinoflagellates, as well as a plethora of single domain transcripts with Type I sequence homology. The current transcriptome analysis compares polyketide synthase (PKS) gene transcripts expressed in two species of Gambierdiscus from French Polynesia: a highly toxic ciguatoxin producer, G. polynesiensis, versus a non-ciguatoxic species G. pacificus, each assembled from approximately 180 million Illumina 125 nt reads using Trinity, and compares their PKS content with previously published data from other Gambierdiscus species and more distantly related dinoflagellates. Both modular and single-domain PKS transcripts were present. Single domain β-ketoacyl synthase (KS) transcripts were highly amplified in both species (98 in G. polynesiensis, 99 in G. pacificus), with smaller numbers of standalone acyl transferase (AT), ketoacyl reductase (KR), dehydratase (DH), enoyl reductase (ER), and thioesterase (TE) domains. G. polynesiensis expressed both a larger number of multidomain PKSs, and larger numbers of modules per transcript, than the non-ciguatoxic G. pacificus. The largest PKS transcript in G. polynesiensis encoded a 10,516 aa, 7 module protein, predicted to synthesize part of the polyether backbone. Transcripts and gene models representing portions of this PKS are present in other species, suggesting that its function may be performed in those species by multiple interacting proteins. This study contributes to the building consensus that dinoflagellates utilize a combination of Type I modular and single domain PKS proteins, in an as yet undefined manner, to synthesize polyketides.

摘要

海洋甲藻产生多种聚酮类毒素,这些毒素在海洋食物网中积累,并导致各种海鲜中毒。与珊瑚礁相关的 Gambierdiscus 属甲藻产生的毒素是造成雪卡中毒(CP)的原因,CP 每年在全球导致超过 50,000 例疾病。甲藻聚酮类化合物的生物合成机制仍知之甚少。最近的转录组和基因组测序项目揭示了甲藻中存在 I 型模块化聚酮合酶,以及大量具有 I 型序列同源性的单结构域转录本。本转录组分析比较了来自法属波利尼西亚的两种 Gambierdiscus 物种中表达的聚酮合酶(PKS)基因转录本:一种是高毒性的雪卡毒素产生者 Gambierdiscus polynesiensis,另一种是非雪卡毒素产生者 Gambierdiscus pacificus,它们分别使用 Trinity 从大约 1.8 亿个 Illumina 125nt 读数组装而成,并将它们的 PKS 含量与之前发表的来自其他 Gambierdiscus 物种和更远缘的甲藻的数据进行了比较。两种模块化和单结构域 PKS 转录本均存在。单结构域β-酮酰基合酶(KS)转录本在两种物种中高度扩增(Gambierdiscus polynesiensis 中 98 个,Gambierdiscus pacificus 中 99 个),独立的酰基转移酶(AT)、酮酰基还原酶(KR)、脱水酶(DH)、烯酰基还原酶(ER)和硫酯酶(TE)结构域数量较少。Gambierdiscus polynesiensis 表达的多域 PKS 数量较多,每个转录本的模块数量也较多。非雪卡毒素产生者 Gambierdiscus pacificus。Gambierdiscus polynesiensis 中最大的 PKS 转录本编码了一个 10516aa、7 个模块的蛋白质,预测它合成了部分聚醚骨架。该 PKS 的转录本和基因模型存在于其他物种中,表明其功能可能由多个相互作用的蛋白质在这些物种中执行。本研究有助于形成共识,即甲藻以尚未定义的方式利用 I 型模块化和单结构域 PKS 蛋白的组合来合成聚酮类化合物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddbb/7159223/794a317f55e3/pone.0231400.g001.jpg

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