Convergent Evolution of Hydrogenosomes from Mitochondria by Gene Transfer and Loss

Autor: Thijs J. G. Ettema, T. Martin Embley, William H Lewis, Kacper M Sendra, Anders E. Lind, Robert P. Hirt, Tom A. Williams, Genoveva F. Esteban, Henning Onsbring
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Mitochondrial DNA
Gene Transfer
Horizontal

Hydrogenosome
Genomics
microbial eukaryotes
Biology
Mitochondrion
Microbiology
Evolution
Molecular

Evolutionsbiologi
03 medical and health sciences
Microbiologie
Convergent evolution
evolution
Genetics
genomics
Anaerobiosis
Ciliophora
Molecular Biology
Ecology
Evolution
Behavior and Systematics

Phylogeny
Discoveries
030304 developmental biology
0303 health sciences
Evolutionary Biology
WIMEK
Sequence Analysis
RNA

Gene Expression Profiling
030302 biochemistry & molecular biology
Biochemistry and Molecular Biology
Sequence Analysis
DNA

biology.organism_classification
anaerobic metabolism
Aerobiosis
Mitochondria
mitochondria
Evolutionary biology
hydrogenosomes
Proteome
Horizontal gene transfer
Genome
Mitochondrial

Biokemi och molekylärbiologi
Archaea
Hydrogen
Zdroj: Molecular Biology and Evolution 37 (2020) 2
Molecular Biology and Evolution
Molecular Biology and Evolution, 37(2), 524-539
Lewis, W, Lind, A, Sendra, K M, Onsbring, H, Williams, T, Esteban, G, Hirt, R P, Ettema, T J G & Embley, T M 2019, ' Convergent evolution of hydrogenosomes from mitochondria by gene transfer and loss ', Molecular Biology and Evolution . https://doi.org/10.1093/molbev/msz239
ISSN: 0737-4038
DOI: 10.1093/molbev/msz239
Popis: Hydrogenosomes are H2-producing mitochondrial homologs found in some anaerobic microbial eukaryotes that provide a rare intracellular niche for H2-utilizing endosymbiotic archaea. Among ciliates, anaerobic and aerobic lineages are interspersed, demonstrating that the switch to an anaerobic lifestyle with hydrogenosomes has occurred repeatedly and independently. To investigate the molecular details of this transition, we generated genomic and transcriptomic data sets from anaerobic ciliates representing three distinct lineages. Our data demonstrate that hydrogenosomes have evolved from ancestral mitochondria in each case and reveal different degrees of independent mitochondrial genome and proteome reductive evolution, including the first example of complete mitochondrial genome loss in ciliates. Intriguingly, the FeFe-hydrogenase used for generating H2 has a unique domain structure among eukaryotes and appears to have been present, potentially through a single lateral gene transfer from an unknown donor, in the common aerobic ancestor of all three lineages. The early acquisition and retention of FeFe-hydrogenase helps to explain the facility whereby mitochondrial function can be so radically modified within this diverse and ecologically important group of microbial eukaryotes.
Databáze: OpenAIRE