Literature DB >> 33684113

The very early evolution of protein translocation across membranes.

A J Harris1,2, Aaron David Goldman2,3.   

Abstract

In this study, we used a computational approach to investigate the early evolutionary history of a system of proteins that, together, embed and translocate other proteins across cell membranes. Cell membranes comprise the basis for cellularity, which is an ancient, fundamental organizing principle shared by all organisms and a key innovation in the evolution of life on Earth. Two related requirements for cellularity are that organisms are able to both embed proteins into membranes and translocate proteins across membranes. One system that accomplishes these tasks is the signal recognition particle (SRP) system, in which the core protein components are the paralogs, FtsY and Ffh. Complementary to the SRP system is the Sec translocation channel, in which the primary channel-forming protein is SecY. We performed phylogenetic analyses that strongly supported prior inferences that FtsY, Ffh, and SecY were all present by the time of the last universal common ancestor of life, the LUCA, and that the ancestor of FtsY and Ffh existed before the LUCA. Further, we combined ancestral sequence reconstruction and protein structure and function prediction to show that the LUCA had an SRP system and Sec translocation channel that were similar to those of extant organisms. We also show that the ancestor of Ffh and FtsY that predated the LUCA was more similar to FtsY than Ffh but could still have comprised a rudimentary protein translocation system on its own. Duplication of the ancestor of FtsY and Ffh facilitated the specialization of FtsY as a membrane bound receptor and Ffh as a cytoplasmic protein that could bind nascent proteins with specific membrane-targeting signal sequences. Finally, we analyzed amino acid frequencies in our ancestral sequence reconstructions to infer that the ancestral Ffh/FtsY protein likely arose prior to or just after the completion of the canonical genetic code. Taken together, our results offer a window into the very early evolutionary history of cellularity.

Entities:  

Year:  2021        PMID: 33684113      PMCID: PMC7987157          DOI: 10.1371/journal.pcbi.1008623

Source DB:  PubMed          Journal:  PLoS Comput Biol        ISSN: 1553-734X            Impact factor:   4.475


  104 in total

1.  Selection of conserved blocks from multiple alignments for their use in phylogenetic analysis.

Authors:  J Castresana
Journal:  Mol Biol Evol       Date:  2000-04       Impact factor: 16.240

Review 2.  Targeting proteins to membranes: structure of the signal recognition particle.

Authors:  Pascal F Egea; Robert M Stroud; Peter Walter
Journal:  Curr Opin Struct Biol       Date:  2005-04       Impact factor: 6.809

3.  Improvement of phylogenies after removing divergent and ambiguously aligned blocks from protein sequence alignments.

Authors:  Gerard Talavera; Jose Castresana
Journal:  Syst Biol       Date:  2007-08       Impact factor: 15.683

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Authors:  F H Crick
Journal:  J Mol Biol       Date:  1968-12       Impact factor: 5.469

5.  On the evolution of the genetic code.

Authors:  C R Woese
Journal:  Proc Natl Acad Sci U S A       Date:  1965-12       Impact factor: 11.205

6.  CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice.

Authors:  J D Thompson; D G Higgins; T J Gibson
Journal:  Nucleic Acids Res       Date:  1994-11-11       Impact factor: 16.971

7.  From decanoate micelles to decanoic acid/dodecylbenzenesulfonate vesicles.

Authors:  Trishool Namani; Peter Walde
Journal:  Langmuir       Date:  2005-07-05       Impact factor: 3.882

8.  The evolution and functional repertoire of translation proteins following the origin of life.

Authors:  Aaron D Goldman; Ram Samudrala; John A Baross
Journal:  Biol Direct       Date:  2010-04-08       Impact factor: 4.540

9.  Structure of the quaternary complex between SRP, SR, and translocon bound to the translating ribosome.

Authors:  Ahmad Jomaa; Yu-Hsien Hwang Fu; Daniel Boehringer; Marc Leibundgut; Shu-Ou Shan; Nenad Ban
Journal:  Nat Commun       Date:  2017-05-19       Impact factor: 14.919

10.  The Pfam protein families database in 2019.

Authors:  Sara El-Gebali; Jaina Mistry; Alex Bateman; Sean R Eddy; Aurélien Luciani; Simon C Potter; Matloob Qureshi; Lorna J Richardson; Gustavo A Salazar; Alfredo Smart; Erik L L Sonnhammer; Layla Hirsh; Lisanna Paladin; Damiano Piovesan; Silvio C E Tosatto; Robert D Finn
Journal:  Nucleic Acids Res       Date:  2019-01-08       Impact factor: 16.971

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  3 in total

1.  A consensus view of the proteome of the last universal common ancestor.

Authors:  Andrew J Crapitto; Amy Campbell; A J Harris; Aaron D Goldman
Journal:  Ecol Evol       Date:  2022-06-03       Impact factor: 3.167

Review 2.  The Dynamic SecYEG Translocon.

Authors:  Julia Oswald; Robert Njenga; Ana Natriashvili; Pinku Sarmah; Hans-Georg Koch
Journal:  Front Mol Biosci       Date:  2021-04-15

3.  A unified evolutionary origin for the ubiquitous protein transporters SecY and YidC.

Authors:  Aaron J O Lewis; Ramanujan S Hegde
Journal:  BMC Biol       Date:  2021-12-15       Impact factor: 7.431

  3 in total

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