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从深海中汲取的经验:真核生物蛋白复合物多样化的机制。

Lessons from the deep: mechanisms behind diversification of eukaryotic protein complexes.

机构信息

Institute of Parasitology, Biology Centre, Czech Academy of Sciences, Branišovská 1160/31, České Budějovice, 37005, Czech Republic.

Faculty of Science, University of South Bohemia, Branišovská 1160/31, České Budějovice, 37005, Czech Republic.

出版信息

Biol Rev Camb Philos Soc. 2023 Dec;98(6):1910-1927. doi: 10.1111/brv.12988. Epub 2023 Jun 19.


DOI:10.1111/brv.12988
PMID:37336550
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10952624/
Abstract

Genetic variation is the major mechanism behind adaptation and evolutionary change. As most proteins operate through interactions with other proteins, changes in protein complex composition and subunit sequence provide potentially new functions. Comparative genomics can reveal expansions, losses and sequence divergence within protein-coding genes, but in silico analysis cannot detect subunit substitutions or replacements of entire protein complexes. Insights into these fundamental evolutionary processes require broad and extensive comparative analyses, from both in silico and experimental evidence. Here, we combine data from both approaches and consider the gamut of possible protein complex compositional changes that arise during evolution, citing examples of complete conservation to partial and total replacement by functional analogues. We focus in part on complexes in trypanosomes as they represent one of the better studied non-animal/non-fungal lineages, but extend insights across the eukaryotes by extensive comparative genomic analysis. We argue that gene loss plays an important role in diversification of protein complexes and hence enhancement of eukaryotic diversity.

摘要

遗传变异是适应和进化变化的主要机制。由于大多数蛋白质是通过与其他蛋白质的相互作用来发挥作用的,因此蛋白质复合物组成和亚基序列的变化提供了潜在的新功能。比较基因组学可以揭示蛋白质编码基因内的扩张、缺失和序列分化,但计算机分析无法检测亚基取代或整个蛋白质复合物的替换。要深入了解这些基本的进化过程,需要从计算机和实验证据两个方面进行广泛而深入的比较分析。在这里,我们结合了这两种方法的数据,并考虑了在进化过程中可能出现的蛋白质复合物组成变化的范围,引用了完整保守到部分和全部由功能类似物替代的例子。我们的重点部分是原生动物中的复合物,因为它们代表了研究较好的非动物/非真菌谱系之一,但通过广泛的比较基因组分析扩展了对真核生物的认识。我们认为,基因丢失在蛋白质复合物的多样化中起着重要作用,从而增强了真核生物的多样性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/a8f141d752a9/BRV-98-1910-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/5c2cf336ffba/BRV-98-1910-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/37e92fa19f75/BRV-98-1910-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/a8f141d752a9/BRV-98-1910-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/5c2cf336ffba/BRV-98-1910-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/37e92fa19f75/BRV-98-1910-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b497/10952624/a8f141d752a9/BRV-98-1910-g003.jpg

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Lessons from the deep: mechanisms behind diversification of eukaryotic protein complexes.

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[3]
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[5]
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本文引用的文献

[1]
The persistent homology of mitochondrial ATP synthases.

iScience. 2023-4-19

[2]
Structural basis of mitochondrial membrane bending by the I-II-III-IV supercomplex.

Nature. 2023-3

[3]
Genome-wide subcellular protein map for the flagellate parasite Trypanosoma brucei.

Nat Microbiol. 2023-3

[4]
Comparative Genomics for Evolutionary Cell Biology Using AMOEBAE: Understanding the Golgi and Beyond.

Methods Mol Biol. 2023

[5]
The mystery of massive mitochondrial complexes: the apicomplexan respiratory chain.

Trends Parasitol. 2022-12

[6]
An ancestral interaction module promotes oligomerization in divergent mitochondrial ATP synthases.

Nat Commun. 2022-10-11

[7]
Combined nanometric and phylogenetic analysis of unique endocytic compartments in Giardia lamblia sheds light on the evolution of endocytosis in Metamonada.

BMC Biol. 2022-9-21

[8]
Mitochondrial complex complexification.

Science. 2022-5-20

[9]
Histone renegades: Unusual H2A histone variants in plants and animals.

Semin Cell Dev Biol. 2023-2-15

[10]
FCHO controls AP2's initiating role in endocytosis through a PtdIns(4,5)P-dependent switch.

Sci Adv. 2022-4-29

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