Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

The Central Dogma01:20

The Central Dogma

20.2K
The central dogma explains the flow of genetic information from DNA nucleotides to the amino acid sequence of proteins.
RNA is the Missing Link Between DNA and Proteins
In the early 1900s, scientists discovered that DNA stores all the information needed for cellular functions and that proteins perform most of these functions. However, the mechanisms of converting genetic information into functional proteins remained unknown for many years. Initially, it was believed that a single gene is...
20.2K
What is Genetic Engineering?00:49

What is Genetic Engineering?

73.4K
Overview
73.4K
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

5.9K
Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
5.9K
From DNA to Protein03:06

From DNA to Protein

17.9K
The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
17.9K
Transgenic Organisms00:53

Transgenic Organisms

30.9K
Overview
30.9K
In-vitro Mutagenesis01:16

In-vitro Mutagenesis

13.7K
To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.
13.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A Pb<sup>2+</sup>-specific DNA G-quadruplex mimic of red fluorescent protein with a monovalent cation ion tolerance.

Journal of inorganic biochemistry·2026
Same author

Solvation chemistry tailored via dielectric constant engineering for stable low-temperature aqueous zinc batteries.

Nature communications·2026
Same author

Magnetic resonance enterography to predict disabling disease in newly diagnosed Crohn's disease: the METRIC-EF multivariable prediction model, multicentre diagnostic inception cohort study.

Health technology assessment (Winchester, England)·2026
Same author

Integrase-On-Demand: bioprospecting integrases for targeted genomic insertion of genetic cargo.

Nucleic acids research·2026
Same author

Engineered orthogonal translation systems from metagenomic libraries expand the genetic code.

bioRxiv : the preprint server for biology·2025
Same author

An updated evolutionary classification of CRISPR-Cas systems including rare variants.

Nature microbiology·2025
Same journal

Inside the new political screening that's stalling NIH grants.

Nature·2026
Same journal

Europe's record heatwave: does the continent have a new climate?

Nature·2026
Same journal

Daily briefing: Humans and great apes giggle in the same rhythms.

Nature·2026
Same journal

The surprising career parallels between footballers and researchers.

Nature·2026
Same journal

I study World Cup penalty shoot-outs: they say a lot about the psychology of performance under pressure.

Nature·2026
Same journal

CRISPR's next act: the companies editing the epigenome to treat disease.

Nature·2026
See all related articles
  1. Home
  2. Engineering A Genomically Recoded Organism With One Stop Codon.
  1. Home
  2. Engineering A Genomically Recoded Organism With One Stop Codon.

Related Experiment Video

Subcloning Plus Insertion SPI - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors
09:02

Subcloning Plus Insertion SPI - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors

Published on: January 8, 2015

16.5K

Engineering a genomically recoded organism with one stop codon.

Michael W Grome1,2, Michael T A Nguyen1,2, Daniel W Moonan2,3

  • 1Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT, USA.

Nature
|February 5, 2025

View abstract on PubMed

Summary
This summary is machine-generated.

Researchers created Ochre, a genomically recoded organism (GRO), by compressing translation functions into single codons. This engineered bacterium uses UAA as its only stop codon, paving the way for a 64-codon non-degenerate genetic code.

More Related Videos

The Production of C. elegans Transgenes via Recombineering with the galK Selectable Marker
12:03

The Production of C. elegans Transgenes via Recombineering with the galK Selectable Marker

Published on: January 11, 2011

14.5K
Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
09:51

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms

Published on: May 25, 2018

33.7K

Related Experiment Videos

Subcloning Plus Insertion SPI - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors
09:02

Subcloning Plus Insertion SPI - A Novel Recombineering Method for the Rapid Construction of Gene Targeting Vectors

Published on: January 8, 2015

16.5K
The Production of C. elegans Transgenes via Recombineering with the galK Selectable Marker
12:03

The Production of C. elegans Transgenes via Recombineering with the galK Selectable Marker

Published on: January 11, 2011

14.5K
Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms
09:51

Enhanced Genome Editing with Cas9 Ribonucleoprotein in Diverse Cells and Organisms

Published on: May 25, 2018

33.7K

Area of Science:

  • Synthetic biology
  • Genomics
  • Molecular biology

Background:

  • The genetic code, while largely conserved, exhibits natural variations in codon assignments and translation factors.
  • Genomically recoded organisms (GROs) have been engineered with alternative genetic codes by replacing synonymous codons.
  • Previous efforts have not fully explored translation factor plasticity and codon degeneracy to achieve a single-codon translational function.

Purpose of the Study:

  • To construct and characterize a GRO, named Ochre, that compresses translational function into a single codon.
  • To assess the feasibility of a non-degenerate genetic code by leveraging codon degeneracy and translation factor engineering.
  • To enable precise production of synthetic proteins with unnatural amino acids for biotechnology and biotherapeutics.

Main Methods:

  • Replaced 1,195 TGA stop codons with synonymous TAA codons in Escherichia coli C321.∆A.
  • Engineered release factor 2 (RF2) and tRNATrp to prevent native UGA recognition.
  • Utilized engineered translation factors to isolate four codons for specific, non-degenerate functions.

Main Results:

  • Successfully constructed Ochre, a GRO with a compressed translational system.
  • Ochre utilizes UAA as the sole stop codon, UGG for tryptophan, and reassigned UAG/UGA codons.
  • Achieved >99% accuracy for multi-site incorporation of two distinct non-standard amino acids into single proteins.

Conclusions:

  • Ochre represents a significant advancement toward a 64-codon non-degenerate genetic code.
  • This engineered organism demonstrates the compression of degenerate stop codons into a single codon.
  • The development of Ochre facilitates the precise synthesis of multi-functional proteins with novel chemistries for broad biotechnological applications.