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Related Concept Videos

Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
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Gene Evolution - Fast or Slow?02:05

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Microorganisms evolve rapidly due to their large population sizes and short generation times, often exhibiting measurable changes within days under laboratory conditions. Natural selection acts on standing genetic variation, enabling the retention and amplification of beneficial traits that confer fitness advantages in changing environments.Adaptive Pigment Regulation in RhodobacterIn Rhodobacter, a genus of purple non-sulfur bacteria, light-harvesting pigments such as bacteriochlorophyll and...
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Understanding the evolutionary relationships among microorganisms is fundamental to microbial ecology and taxonomy. Phylogenetic trees are essential tools for inferring these relationships, relying primarily on comparative analyses of molecular sequences such as DNA, RNA, or proteins. In microbial studies, these trees typically depict the evolutionary paths of diverse bacterial and archaeal species by mapping genetic differences accumulated over time.Phylogenetic trees are composed of tips,...
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Using Phylogenetic Analysis to Investigate Eukaryotic Gene Origin
08:57

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Published on: August 14, 2018

Protein evolution along phylogenetic histories under structurally constrained substitution models.

Miguel Arenas1, Helena G Dos Santos, David Posada

  • 1Centre for Molecular Biology 'Severo Ochoa', Consejo Superior de Investigaciones Científicas (CSIC), Madrid, Spain and Department of Biochemistry, Genetics and Immunology, University of Vigo, Vigo, Spain.

Bioinformatics (Oxford, England)
|September 17, 2013
PubMed
Summary

Simulating protein evolution using stability and realistic evolutionary histories generates more accurate amino acid distributions and stable proteins. This approach improves in silico protein evolution modeling for research.

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Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues
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Optimization of Synthetic Proteins: Identification of Interpositional Dependencies Indicating Structurally and/or Functionally Linked Residues

Published on: July 14, 2015

Area of Science:

  • Molecular Evolution
  • Computational Biology
  • Structural Bioinformatics

Background:

  • Current molecular evolution models often neglect protein structure information.
  • Structure-based protein evolution models are not widely used in phylogenetic analyses and may overlook processes like recombination.

Purpose of the Study:

  • To develop a simulation framework integrating protein stability and phylogenetic histories for realistic in silico protein evolution.
  • To generate more accurate in silico evolved proteins by accounting for folding stability and evolutionary processes.

Main Methods:

  • Developed a method combining protein folding stability models (considering unfolding and misfolding) with phylogenetic histories.
  • Integrated complex evolutionary scenarios, including recombination, demographics, and migration.
  • Implemented the framework in a program named ProteinEvolver.

Main Results:

  • The new models produced amino acid distributions more closely resembling those in real protein families compared to empirical models.
  • Proteins simulated using this framework were predicted to be more stable.
  • The ProteinEvolver program was developed to facilitate these simulations.

Conclusions:

  • Evolutionary models incorporating protein stability and realistic evolutionary histories provide a better approximation of the actual evolutionary process.
  • This integrated approach enhances the realism of in silico protein evolution for various applications.
  • The findings suggest a significant improvement in simulating protein evolution by considering structural stability.