» Articles » PMID: 32731621

Evidence Supporting an Antimicrobial Origin of Targeting Peptides to Endosymbiotic Organelles

Overview
Journal Cells
Publisher MDPI
Date 2020 Aug 1
PMID 32731621
Citations 12
Authors
Affiliations
Soon will be listed here.
Abstract

Mitochondria and chloroplasts emerged from primary endosymbiosis. Most proteins of the endosymbiont were subsequently expressed in the nucleo-cytosol of the host and organelle-targeted via the acquisition of -terminal presequences, whose evolutionary origin remains enigmatic. Using a quantitative assessment of their physico-chemical properties, we show that organelle targeting peptides, which are distinct from signal peptides targeting other subcellular compartments, group with a subset of antimicrobial peptides. We demonstrate that extant antimicrobial peptides target a fluorescent reporter to either the mitochondria or the chloroplast in the green alga and, conversely, that extant targeting peptides still display antimicrobial activity. Thus, we provide strong computational and functional evidence for an evolutionary link between organelle-targeting and antimicrobial peptides. Our results support the view that resistance of bacterial progenitors of organelles to the attack of host antimicrobial peptides has been instrumental in eukaryogenesis and in the emergence of photosynthetic eukaryotes.

Citing Articles

Regulation of chloroplast biogenesis, development, and signaling by endogenous and exogenous cues.

Mahapatra K, Mukherjee A, Suyal S, Dar M, Bhagavatula L, Datta S Physiol Mol Biol Plants. 2024; 30(2):167-183.

PMID: 38623168 PMC: 11016055. DOI: 10.1007/s12298-024-01427-8.


Understanding protein import in diverse non-green plastids.

Christian R, Labbancz J, Usadel B, Dhingra A Front Genet. 2023; 14:969931.

PMID: 37007964 PMC: 10063809. DOI: 10.3389/fgene.2023.969931.


Converting antimicrobial into targeting peptides reveals key features governing protein import into mitochondria and chloroplasts.

Caspari O, Garrido C, Law C, Choquet Y, Wollman F, Lafontaine I Plant Commun. 2023; 4(4):100555.

PMID: 36733255 PMC: 10363480. DOI: 10.1016/j.xplc.2023.100555.


A mitochondrion-free eukaryote contains proteins capable of import into an exogenous mitochondrion-related organelle.

Fang Y, Vaitova Z, Hampl V Open Biol. 2023; 13(1):220238.

PMID: 36629021 PMC: 9832562. DOI: 10.1098/rsob.220238.


Increasing the Efficiency of the Accumulation of Recombinant Proteins in Plant Cells: The Role of Transport Signal Peptides.

Rozov S, Deineko E Plants (Basel). 2022; 11(19).

PMID: 36235427 PMC: 9572730. DOI: 10.3390/plants11192561.


References
1.
Doolittle W . You are what you eat: a gene transfer ratchet could account for bacterial genes in eukaryotic nuclear genomes. Trends Genet. 1998; 14(8):307-11. DOI: 10.1016/s0168-9525(98)01494-2. View

2.
Schatz G, Dobberstein B . Common principles of protein translocation across membranes. Science. 1996; 271(5255):1519-26. DOI: 10.1126/science.271.5255.1519. View

3.
Runti G, Lopez Ruiz M, Stoilova T, Hussain R, Jennions M, Choudhury H . Functional characterization of SbmA, a bacterial inner membrane transporter required for importing the antimicrobial peptide Bac7(1-35). J Bacteriol. 2013; 195(23):5343-51. PMC: 3837949. DOI: 10.1128/JB.00818-13. View

4.
Huang J, Hack E, Thornburg R, Myers A . A yeast mitochondrial leader peptide functions in vivo as a dual targeting signal for both chloroplasts and mitochondria. Plant Cell. 1990; 2(12):1249-60. PMC: 159970. DOI: 10.1105/tpc.2.12.1249. View

5.
Besse A, Peduzzi J, Rebuffat S, Carre-Mlouka A . Antimicrobial peptides and proteins in the face of extremes: Lessons from archaeocins. Biochimie. 2015; 118:344-55. DOI: 10.1016/j.biochi.2015.06.004. View