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Related Concept Videos

Mismatch Repair01:20

Mismatch Repair

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
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Mutations01:35

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Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
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Mutations in Microorganisms01:18

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Mutations are heritable changes in an organism’s genome involving alterations in the base sequence of DNA or RNA. These changes can influence cellular processes and phenotypic traits, potentially transforming the unaltered wild type into a mutant form. Such changes, termed forward mutations, are pivotal in shaping the genetic diversity of organisms.RNA viruses exhibit the highest mutation rates due to the absence of robust proofreading mechanisms during genome replication. In contrast,...
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In-vitro Mutagenesis01:16

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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.
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Spontaneous and Induced Mutations01:30

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Spontaneous mutations arise infrequently during DNA replication due to errors in the process. A key factor behind these errors is tautomeric shifts in nitrogenous bases, where bases transition from keto to enol forms or amino to imino forms. This shift can alter base-pairing rules, leading to mutations. Additionally, reactive oxygen species (ROS) arising from aerobic metabolism can damage DNA, resulting in depurination (loss of a purine base) or depyrimidination (loss of a pyrimidine base).
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Predicting mutational function using machine learning.

Anthony Shea1, Josh Bartz2, Lei Zhang3

  • 1Institute on the Biology of Aging and Metabolism, University of Minnesota, Minneapolis, MN 55455, USA; Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455, USA.

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Computational approaches, particularly machine learning (ML), are advancing our ability to understand how genetic variations and mutations contribute to human diseases and aging. These methods help analyze the vastness of genomic data to predict functional impacts.

Keywords:
Disease RiskGene ExpressionMachine LearningMutationProtein Structure

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Area of Science:

  • Genomics
  • Computational Biology
  • Bioinformatics

Background:

  • Genetic variations, including germline and somatic mutations, are fundamental to human phenotypic diversity and disease.
  • The sheer volume of genetic variations presents a significant challenge for experimental functional verification.
  • Computational methods, especially machine learning, offer powerful tools to address this challenge.

Purpose of the Study:

  • To review recent progress in computational approaches for understanding mutation function.
  • To classify and discuss various machine learning models used in this field.
  • To highlight future directions for computational genomics in aging and disease research.

Main Methods:

  • Classification of computational models based on prediction goals (protein structure, gene expression, disease risk).
  • Classification of models based on methodologies (non-ML, classical ML, deep neural networks).
  • Discussion of model architecture, accuracy, and limitations.

Main Results:

  • Significant advancements have been made in applying computational models to predict the functional impact of genetic variations.
  • Machine learning models demonstrate increasing accuracy in diverse prediction tasks related to mutations.
  • The review categorizes and analyzes a wide range of computational strategies.

Conclusions:

  • Computational approaches, especially machine learning, are crucial for deciphering the complex roles of genetic mutations in human health and disease.
  • Future research should focus on refining these models and exploring novel applications in aging and disease.
  • This review provides a comprehensive overview and insights into the evolving field of computational mutation effect prediction.