A New Model and Dating for the Evolution of Complex Plastids of Red Alga Origin.

IF 3.2 2区 生物学 Q2 EVOLUTIONARY BIOLOGY Genome Biology and Evolution Pub Date : 2024-09-03 DOI:10.1093/gbe/evae192
Filip Pietluch, Paweł Mackiewicz, Kacper Ludwig, Przemysław Gagat
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Abstract

Complex plastids, characterized by more than two bounding membranes, still present an evolutionary puzzle for the traditional endosymbiotic theory. Unlike primary plastids that directly evolved from cyanobacteria, complex plastids originated from green or red algae. The Chromalveolata hypothesis proposes a single red alga endosymbiosis that involved the ancestor of all the Chromalveolata lineages: cryptophytes, haptophytes, stramenopiles, and alveolates. As extensive phylogenetic analyses contradict the monophyly of Chromalveolata, serial plastid endosymbiosis models were proposed, suggesting a single secondary red alga endosymbiosis within Cryptophyta, followed by subsequent plastid transfers to other chromalveolates. Our findings based on 97 plastid-encoded markers, 112 species, and robust phylogenetic methods challenge all the existing models. They reveal two independent secondary endosymbioses, one within Cryptophyta and one within stramenopiles, precisely the phylum Ochrophyta, with two different groups of red algae. Consequently, we propose a new model for the emergence of red alga plastid-containing lineages and, through molecular clock analyses, estimate their ages.

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红藻起源复杂质体进化的新模型和年代测定。
复杂质体的特点是有两层以上的结合膜,它仍然是传统内共生理论的一个进化难题。与直接从蓝藻进化而来的初级质体不同,它们起源于绿藻或红藻。Chromalveolata 假说提出了一个单一的红藻内共生理论,涉及所有 Chromalveolata 系的祖先:隐藻、隐藻、担子藻和肺泡藻。由于广泛的系统发育分析与红藻单系的观点相矛盾,因此有人提出了系列质体共生模型,认为在隐藻门内存在单一的次级红藻共生,随后质体转移到其他色界藻。我们的研究结果基于 97 个质体编码标记、112 个物种和强大的系统发生学方法,对所有现有模式提出了挑战。它们揭示了两个独立的次生共生现象,一个在隐藻门内,另一个在担子菌门内,准确地说是在水藻门内,与两个不同的红藻群共生。因此,我们为含质体红藻系的出现提出了一个新的模型,并通过分子钟分析估算了它们的年龄。
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来源期刊
Genome Biology and Evolution
Genome Biology and Evolution EVOLUTIONARY BIOLOGY-GENETICS & HEREDITY
CiteScore
5.80
自引率
6.10%
发文量
169
审稿时长
1 months
期刊介绍: About the journal Genome Biology and Evolution (GBE) publishes leading original research at the interface between evolutionary biology and genomics. Papers considered for publication report novel evolutionary findings that concern natural genome diversity, population genomics, the structure, function, organisation and expression of genomes, comparative genomics, proteomics, and environmental genomic interactions. Major evolutionary insights from the fields of computational biology, structural biology, developmental biology, and cell biology are also considered, as are theoretical advances in the field of genome evolution. GBE’s scope embraces genome-wide evolutionary investigations at all taxonomic levels and for all forms of life — within populations or across domains. Its aims are to further the understanding of genomes in their evolutionary context and further the understanding of evolution from a genome-wide perspective.
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