Literature DB >> 20534711

Origin and evolution of the ribosome.

George E Fox1.   

Abstract

The modern ribosome was largely formed at the time of the last common ancestor, LUCA. Hence its earliest origins likely lie in the RNA world. Central to its development were RNAs that spawned the modern tRNAs and a symmetrical region deep within the large ribosomal RNA, (rRNA), where the peptidyl transferase reaction occurs. To understand pre-LUCA developments, it is argued that events that are coupled in time are especially useful if one can infer a likely order in which they occurred. Using such timing events, the relative age of various proteins and individual regions within the large rRNA are inferred. An examination of the properties of modern ribosomes strongly suggests that the initial peptides made by the primitive ribosomes were likely enriched for l-amino acids, but did not completely exclude d-amino acids. This has implications for the nature of peptides made by the first ribosomes. From the perspective of ribosome origins, the immediate question regarding coding is when did it arise rather than how did the assignments evolve. The modern ribosome is very dynamic with tRNAs moving in and out and the mRNA moving relative to the ribosome. These movements may have become possible as a result of the addition of a template to hold the tRNAs. That template would subsequently become the mRNA, thereby allowing the evolution of the code and making an RNA genome useful. Finally, a highly speculative timeline of major events in ribosome history is presented and possible future directions discussed.

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Year:  2010        PMID: 20534711      PMCID: PMC2926754          DOI: 10.1101/cshperspect.a003483

Source DB:  PubMed          Journal:  Cold Spring Harb Perspect Biol        ISSN: 1943-0264            Impact factor:   10.005


  121 in total

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Authors:  Ella Zimmerman; Ada Yonath
Journal:  Chembiochem       Date:  2009-01-05       Impact factor: 3.164

2.  Requirement of the RNA helicase-like protein PRP22 for release of messenger RNA from spliceosomes.

Authors:  M Company; J Arenas; J Abelson
Journal:  Nature       Date:  1991-02-07       Impact factor: 49.962

3.  D-Tyrosyl RNA: formation, hydrolysis and utilization for protein synthesis.

Authors:  R Calendar; P Berg
Journal:  J Mol Biol       Date:  1967-05-28       Impact factor: 5.469

4.  Ribosomal binding and dipeptide formation by misacylated tRNA(Phe),S.

Authors:  T G Heckler; J R Roesser; C Xu; P I Chang; S M Hecht
Journal:  Biochemistry       Date:  1988-09-20       Impact factor: 3.162

5.  The eIF1A solution structure reveals a large RNA-binding surface important for scanning function.

Authors:  J L Battiste; T V Pestova; C U Hellen; G Wagner
Journal:  Mol Cell       Date:  2000-01       Impact factor: 17.970

6.  The structure of T. aquaticus DNA polymerase III is distinct from eukaryotic replicative DNA polymerases.

Authors:  Scott Bailey; Richard A Wing; Thomas A Steitz
Journal:  Cell       Date:  2006-09-08       Impact factor: 41.582

7.  Synthesis of activated pyrimidine ribonucleotides in prebiotically plausible conditions.

Authors:  Matthew W Powner; Béatrice Gerland; John D Sutherland
Journal:  Nature       Date:  2009-05-14       Impact factor: 49.962

8.  Enhanced D-amino acid incorporation into protein by modified ribosomes.

Authors:  Larisa M Dedkova; Nour Eddine Fahmi; Serguei Y Golovine; Sidney M Hecht
Journal:  J Am Chem Soc       Date:  2003-06-04       Impact factor: 15.419

9.  Functional evolution of two subtly different (similar) folds.

Authors:  V Agrawal; R K Kishan
Journal:  BMC Struct Biol       Date:  2001-12-21

10.  Ribosomal RNAs are tolerant toward genetic insertions: evolutionary origin of the expansion segments.

Authors:  Takeshi Yokoyama; Tsutomu Suzuki
Journal:  Nucleic Acids Res       Date:  2008-05-02       Impact factor: 16.971

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  86 in total

1.  An exit cavity was crucial to the polymerase activity of the early ribosome.

Authors:  George E Fox; Quyen Tran; Ada Yonath
Journal:  Astrobiology       Date:  2011-12-22       Impact factor: 4.335

2.  Domain III of the T. thermophilus 23S rRNA folds independently to a near-native state.

Authors:  Shreyas S Athavale; J Jared Gossett; Chiaolong Hsiao; Jessica C Bowman; Eric O'Neill; Eli Hershkovitz; Thanawadee Preeprem; Nicholas V Hud; Roger M Wartell; Stephen C Harvey; Loren Dean Williams
Journal:  RNA       Date:  2012-02-14       Impact factor: 4.942

3.  Nucleolar dominance and maternal control of 45S rDNA expression.

Authors:  Katarzyna Michalak; Sebastian Maciak; Young Bun Kim; Graciela Santopietro; Jung Hun Oh; Lin Kang; Harold R Garner; Pawel Michalak
Journal:  Proc Biol Sci       Date:  2015-12-07       Impact factor: 5.349

4.  History of the ribosome and the origin of translation.

Authors:  Anton S Petrov; Burak Gulen; Ashlyn M Norris; Nicholas A Kovacs; Chad R Bernier; Kathryn A Lanier; George E Fox; Stephen C Harvey; Roger M Wartell; Nicholas V Hud; Loren Dean Williams
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-30       Impact factor: 11.205

Review 5.  Paradigms of ribosome synthesis: Lessons learned from ribosomal proteins.

Authors:  Michael Gamalinda; John L Woolford
Journal:  Translation (Austin)       Date:  2015-02-02

6.  The minimotif synthesis hypothesis for the origin of life.

Authors:  Martin R Schiller
Journal:  J Transl Sci       Date:  2016-07-19

7.  Heterologous Inferential Analysis (HIA) and Other Emerging Concepts: In Understanding Mitochondrial Variation In Pathogenesis: There is no More Low-Hanging Fruit.

Authors:  Antón Vila-Sanjurjo; Paul M Smith; Joanna L Elson
Journal:  Methods Mol Biol       Date:  2021

8.  Differences in the path to exit the ribosome across the three domains of life.

Authors:  Khanh Dao Duc; Sanjit S Batra; Nicholas Bhattacharya; Jamie H D Cate; Yun S Song
Journal:  Nucleic Acids Res       Date:  2019-05-07       Impact factor: 16.971

Review 9.  The protein invasion: a broad review on the origin of the translational system.

Authors:  David W Morgens
Journal:  J Mol Evol       Date:  2013-10-22       Impact factor: 2.395

10.  Protosemiosis: agency with reduced representation capacity.

Authors:  Alexei A Sharov; Tommi Vehkavaara
Journal:  Biosemiotics       Date:  2015-04-01       Impact factor: 0.711

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