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Improving Translational Accuracy02:07

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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...
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Coordination of Gene Expression Processes in Bacteria01:29

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The DNA replication, transcription, and translation processes are intricately coupled in bacteria, allowing efficient gene expression and rapid protein synthesis. While this physical and functional coordination is advantageous, it introduces challenges that bacteria overcome through specific regulatory mechanisms.Coupling of Replication, Transcription, and TranslationThe coupling of replication, transcription, and translation is a hallmark of bacterial gene expression. As the replisome unwinds...
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DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
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Transcriptional attenuation occurs when RNA transcription is prematurely terminated due to the formation of a terminator mRNA hairpin structure.  Bacteria use these hairpins to regulate the transcription process and control the synthesis of several amino acids including histidine, lysine, threonine, and phenylalanine. Transcription attenuation takes place in the non-coding regions of mRNA.
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Genome-wide Surveillance of Transcription Errors in Eukaryotic Organisms
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Universally high transcript error rates in bacteria.

Weiyi Li1, Michael Lynch1,2

  • 1Department of Biology, Indiana University, Bloomington, United States.

Elife
|May 30, 2020
PubMed
Summary
This summary is machine-generated.

Genetic transcription errors are far more common than previously thought, occurring at rates 1000 times higher than mutations. These errors can alter protein sequences and suggest a quality control mechanism in prokaryotes.

Keywords:
B. subtilisE. coliRNA quality-controlbase substitutionschromosomesgene expressiongeneticsgenomicstranscript errorstranscriptional fidelity

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Area of Science:

  • Molecular Biology
  • Genetics
  • Microbiology

Background:

  • Genetic mutations from replication errors are well-studied.
  • Transcript errors, their rates, and effects remain largely unknown.

Purpose of the Study:

  • To globally identify and characterize transcript errors in prokaryotes.
  • To determine the rate, molecular spectrum, and functional impact of transcription errors.

Main Methods:

  • Utilized an adapted rolling-circle sequencing approach.
  • Analyzed transcript errors in *Escherichia coli*, *Bacillus subtilis*, *Agrobacterium tumefaciens*, and *Mesoplasma florum*.

Main Results:

  • Transcript error rates were 3-4 orders of magnitude higher than mutation rates.
  • Most errors, if translated, would cause amino acid changes.
  • Identified detailed molecular spectrum and distribution of errors across 9929 loci.
  • Observed a G→A substitution bias in *M. florum*, indicating an error-prone RNA polymerase.
  • Found increased nonsense errors at the 3' end of mRNAs.

Conclusions:

  • Transcription errors are frequent and can significantly impact protein sequences.
  • A Nonsense-Mediated Decay-like quality control mechanism may exist in prokaryotes.