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来自具有复杂细胞生物学的最后共同祖先(LUCA)的古老且高度保守的蛋白质为核区室共性(NuCom)假说提供了支持证据。

Ancient, highly conserved proteins from a LUCA with complex cell biology provide evidence in support of the nuclear compartment commonality (NuCom) hypothesis.

作者信息

Staley James T, Fuerst John A

机构信息

Department of Microbiology and Astrobiology Program, University of Washington, Seattle 98195, USA.

School of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, Queensland 4072, Australia.

出版信息

Res Microbiol. 2017 Jun;168(5):395-412. doi: 10.1016/j.resmic.2017.01.001. Epub 2017 Jan 19.

DOI:10.1016/j.resmic.2017.01.001
PMID:28111289
Abstract

The nuclear compartment commonality (NuCom) hypothesis posits a complex last common ancestor (LUCA) with membranous compartments including a nuclear membrane. Such a LUCA then evolved to produce two nucleated lineages of the tree of life: the Planctomycetes-Verrucomicrobia-Chlamydia superphylum (PVC) within the Bacteria, and the Eukarya. We propose that a group of ancient essential protokaryotic signature proteins (PSPs) originating in LUCA were incorporated into ancestors of PVC Bacteria and Eukarya. Tubulins, ubiquitin system enzymes and sterol-synthesizing enzymes are consistent with early origins of these features shared between the PVC superphylum and Eukarya.

摘要

核区室共性(NuCom)假说假定存在一个具有膜性区室(包括核膜)的复杂的最后共同祖先(LUCA)。这样一个LUCA随后进化产生了生命树的两个有核谱系:细菌中的浮霉菌-疣微菌-衣原体超门(PVC)和真核生物。我们提出,一组起源于LUCA的古老的必需原核生物标志性蛋白(PSP)被纳入了PVC细菌和真核生物的祖先中。微管蛋白、泛素系统酶和固醇合成酶与PVC超门和真核生物之间共享的这些特征的早期起源是一致的。

相似文献

1
Ancient, highly conserved proteins from a LUCA with complex cell biology provide evidence in support of the nuclear compartment commonality (NuCom) hypothesis.来自具有复杂细胞生物学的最后共同祖先(LUCA)的古老且高度保守的蛋白质为核区室共性(NuCom)假说提供了支持证据。
Res Microbiol. 2017 Jun;168(5):395-412. doi: 10.1016/j.resmic.2017.01.001. Epub 2017 Jan 19.
2
Domain Cell Theory supports the independent evolution of the Eukarya, Bacteria and Archaea and the Nuclear Compartment Commonality hypothesis.领域细胞理论支持真核生物、细菌和古菌的独立进化以及核区室共性假说。
Open Biol. 2017 Jun;7(6). doi: 10.1098/rsob.170041.
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Signature protein of the PVC superphylum.PVC超门的标志性蛋白。
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Planctomycetes and eukaryotes: a case of analogy not homology.厚壁菌门和真核生物:类似而非同源。
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The PVC superphylum: exceptions to the bacterial definition?聚氯乙烯超级门:细菌定义的例外?
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Investigation of tRNA-based relatedness within the Planctomycetes-Verrucomicrobia-Chlamydiae (PVC) superphylum: a comparative analysis.研究厚壁菌门-浮霉菌门-螺旋体门(PVC)超级门内基于 tRNA 的相关性:比较分析。
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Phylum Verrucomicrobia representatives share a compartmentalized cell plan with members of bacterial phylum Planctomycetes.疣微菌门的代表与浮霉菌门的细菌成员具有分区化的细胞结构。
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Proteins Related to the Type I Secretion System Are Associated with Secondary SecA_DEAD Domain Proteins in Some Species of Planctomycetes, Verrucomicrobia, Proteobacteria, Nitrospirae and Chlorobi.与Ⅰ型分泌系统相关的蛋白质在浮霉菌门、疣微菌门、变形菌门、硝化螺旋菌门和绿弯菌门的某些物种中与Ⅱ型SecA_DEAD结构域蛋白相关。
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The compartmentalized bacteria of the planctomycetes-verrucomicrobia-chlamydiae superphylum have membrane coat-like proteins.厚壁菌门-浮霉菌门-螺旋体菌超门的分隔细菌具有膜壳状蛋白。
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Molecular Signatures for the PVC Clade (Planctomycetes, Verrucomicrobia, Chlamydiae, and Lentisphaerae) of Bacteria Provide Insights into Their Evolutionary Relationships.细菌的 PVC 分支(浮霉菌门、疣微菌门、衣原体和 Lentisphaerae)的分子特征为其进化关系提供了新的见解。
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引用本文的文献

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The Last Universal Common Ancestor of Ribosome-Encoding Organisms: Portrait of LUCA.核糖体编码生物的最后一个普遍共同祖先:LUCA 画像。
J Mol Evol. 2024 Oct;92(5):550-583. doi: 10.1007/s00239-024-10186-9. Epub 2024 Aug 19.
2
The Origin(s) of Cell(s): Pre-Darwinian Evolution from FUCAs to LUCA : To Carl Woese (1928-2012), for his Conceptual Breakthrough of Cellular Evolution.细胞的起源(起源):从 FUCAs 到 LUCA 的达尔文前进化:献给卡尔·伍斯(1928-2012),他在细胞进化的概念突破方面做出了贡献。
J Mol Evol. 2021 Aug;89(7):427-447. doi: 10.1007/s00239-021-10014-4. Epub 2021 Jun 25.
3
Manifold Routes to a Nucleus.
通向细胞核的多种途径。
Front Microbiol. 2018 Oct 26;9:2604. doi: 10.3389/fmicb.2018.02604. eCollection 2018.
4
Domain Cell Theory supports the independent evolution of the Eukarya, Bacteria and Archaea and the Nuclear Compartment Commonality hypothesis.领域细胞理论支持真核生物、细菌和古菌的独立进化以及核区室共性假说。
Open Biol. 2017 Jun;7(6). doi: 10.1098/rsob.170041.