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Related Concept Videos

From DNA to Protein03:06

From DNA to Protein

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...
Leaky Scanning02:28

Leaky Scanning

During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R stands for...
Transfer RNA Synthesis02:36

Transfer RNA Synthesis

One of the unique features of tRNA is the presence of modified bases. In some tRNAs, modified bases account for nearly 20% of the total bases in the molecule. Altogether, these unusual bases protect the tRNA from enzymatic degradation by RNases.
Each of these chemical modifications is carried by a specific enzyme, post-transcription. All of these enzymes have unique base and site-specificity. Methylation, the most common chemical modification, is carried by at least nine different enzymes, with...
Improving Translational Accuracy02:07

Improving Translational Accuracy

Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
Termination of Translation01:44

Termination of Translation

The large ribosomal subunit has several important structures essential to translation. These include the peptidyl transferase center (PTC) - which is the site where the peptide bond is formed - and a large, internal, water-filled tube through which the nascent polypeptide moves. This latter structure is called the Peptide Exit Tunnel, and it begins at the PTC and spans the body of the large ribosomal subunit. During translation, as the nascent polypeptide chain is synthesized, it passes through...
tRNA Activation02:26

tRNA Activation

Aminoacyl-tRNA synthetases are present in both eukaryotes and bacteria. Though eukaryotes have 20 different aminoacyl-tRNA synthetases to couple to 20 amino acids, many bacteria do not have genes for all of these aminoacyl-tRNA synthetases. Despite this, they still use all 20 amino acids to synthesize their proteins. For instance, some bacteria do not have the gene encoding the enzyme that couples glutamine with its partner tRNA. In these organisms, one enzyme adds glutamic acid to all of the...

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Tandem Affinity Purification of Protein Complexes from Eukaryotic Cells
11:30

Tandem Affinity Purification of Protein Complexes from Eukaryotic Cells

Published on: January 26, 2017

Tandem stop codons in ciliates that reassign stop codons.

Marie Adachi1, Andre R O Cavalcanti

  • 1Biology Department, Pomona College, 175 West 6th Street, Claremont, CA 91711, USA. ma002005@mymail.pomona.edu

Journal of Molecular Evolution
|March 19, 2009
PubMed
Summary
This summary is machine-generated.

Tandem stop codons, backup genetic signals, were found more often than expected in Paramecium tetraurelia and Tetrahymena thermophila. This suggests higher stop codon read-through in these species due to altered genetic codes.

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Last Updated: Jun 24, 2026

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Published on: January 26, 2017

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Area of Science:

  • Genetics
  • Molecular Biology
  • Evolutionary Biology

Background:

  • Tandem stop codons are hypothesized genetic backup mechanisms.
  • While absent in E. coli, they are confirmed in yeast.
  • Ciliates like Paramecium and Tetrahymena reassign standard stop codons (TAA, TAG) to glutamine.

Purpose of the Study:

  • To investigate the presence and frequency of tandem stop codons in two ciliate species: Paramecium tetraurelia and Tetrahymena thermophila.
  • To compare tandem stop codon occurrence in these ciliates with yeast and bacterial systems.

Main Methods:

  • Genome analysis of Paramecium tetraurelia and Tetrahymena thermophila.
  • Statistical analysis of tandem stop codon distribution downstream of genes.
  • Comparison of observed frequencies with those expected based on local base composition.

Main Results:

  • Both Paramecium and Tetrahymena exhibit a significant excess of tandem stop codons downstream of genes.
  • The frequency of tandem stop codons is higher in these ciliates than in yeast.
  • The observed excess is greater than what can be explained by random chance or base composition alone.

Conclusions:

  • The findings support the presence of tandem stop codons in ciliates with reassigned stop codons.
  • A higher frequency of stop codon read-through is proposed for Paramecium and Tetrahymena compared to yeast.
  • This may be attributed to a less efficient translational termination system resulting from stop codon reassignment.