Evidence map›Paper›PMID 34561441›Full record

ArticleNature communications2021

Directed evolution of rRNA improves translation kinetics and recombinant protein yield.

Fan Liu, Siniša Bratulić, Alan Costello, Teemu P Miettinen, Ahmed H Badran

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 25 citations in OpenAlex.

  1. Ribosome engineering enhances genetic code expansion inSynthetic and systems biotechnology · 2027
    Article
  2. Dynamic evolution and hierarchical regulation of rDNA in polyploid oat.The Plant journal : for cell and molecular biology · 2026
    Article
  3. Article
  4. Article
  5. Biomanufacturing Potential of Streamlined Cells.Biotechnology and bioengineering · 2025
    Article
  6. Article
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. RNA language models predict mutations that improve RNA function.bioRxiv : the preprint server for biology · 2024
    Article
  13. Review
  14. Socialized mitochondria: mitonuclear crosstalk in stress.Experimental & molecular medicine · 2024
    Review
  15. Virus-assisted directed evolution of biomolecules.Current opinion in chemical biology · 2023
    Review
  16. Cell-free Biosynthesis of Peptidomimetics.Biotechnology and bioprocess engineering : BBE · 2023
    Review
  17. Review
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Fan Liu *The Broad Institute of MIT & Harvard University, Cambridge, MA, 02142, USA.ORCID 0000-0002-4333-7581
Siniša Bratulić *The Broad Institute of MIT & Harvard University, Cambridge, MA, 02142, USA.ORCID 0000-0002-1663-2227
Alan Costello *The Broad Institute of MIT & Harvard University, Cambridge, MA, 02142, USA.ORCID 0000-0002-6266-5070
Teemu P MiettinenKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, MA, 02142, USA.ORCID 0000-0002-5975-200X
Ahmed H BadranThe Broad Institute of MIT & Harvard University, Cambridge, MA, 02142, USA. ahbadran@scripps.edu.ORCID 0000-0002-8105-1883
Broad Institute · USMassachusetts Institute of Technology · US

Funding

Functional Interrogation Of Ribosomal Biology Using Continuous EvolutionDP5OD024590 · OD · SCRIPPS RESEARCH INSTITUTE, THE · PI BADRAN, AHMED HUSSEIN · 2017 to 2021
$2.2M
NIH HHS DP5 OD024590
6 · The paper itself

Abstract

In bacteria, ribosome kinetics are considered rate-limiting for protein synthesis and cell growth. Enhanced ribosome kinetics may augment bacterial growth and biomanufacturing through improvements to overall protein yield, but whether this can be achieved by ribosome-specific modifications remains unknown. Here, we evolve 16S ribosomal RNAs (rRNAs) from Escherichia coli, Pseudomonas aeruginosa, and Vibrio cholerae towards enhanced protein synthesis rates. We find that rRNA sequence origin significantly impacted evolutionary trajectory and generated rRNA mutants with augmented protein synthesis rates in both natural and engineered contexts, including the incorporation of noncanonical amino acids. Moreover, discovered consensus mutations can be ported onto phylogenetically divergent rRNAs, imparting improved translational activities. Finally, we show that increased translation rates in vivo coincide with only moderately reduced translational fidelity, but do not enhance bacterial population growth. Together, these findings provide a versatile platform for development of unnatural ribosomal functions in vivo.

Indexed as

Protein BiosynthesisBase SequenceDirected Molecular EvolutionEscherichia coliKineticsMass SpectrometryModels, MolecularMutationNucleic Acid ConformationProteomeRecombinant ProteinsRibosomal ProteinsRibosomesRNA, RibosomalRNA, Ribosomal, 16SProteomeRecombinant ProteinsRibosomal ProteinsRNA, RibosomalRNA, Ribosomal, 16S

Identifiers

PMID34561441
PMCPMC8463689
OpenAlexW3199575259

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.