Upon Accounting for the Impact of Isoenzyme Loss, Gene Deletion Costs Anticorrelate with Their Evolutionary Rates

Abstract

System-level metabolic network models enable the computation of growth and metabolic phenotypes from an organism's genome. In particular, flux balance approaches have been used to estimate the contribution of individual metabolic genes to organismal fitness, offering the opportunity to test whether such contributions carry information about the evolutionary pressure on the corresponding genes. Previous failure to identify the expected negative correlation between such computed gene-loss cost and sequence-derived evolutionary rates in Saccharomyces cerevisiae has been ascribed to a real biological gap between a gene's fitness contribution to an organism here and now and the same gene's historical importance as evidenced by its accumulated mutations over millions of years of evolution. Here we show that this negative correlation does exist, and can be exposed by revisiting a broadly employed assumption of flux balance models.

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Document Details

Document Type
Technical Report
Publication Date
Jan 20, 2017
Accession Number
AD1057738

Entities

People

  • Christopher Jacobs
  • Daniel Segrè
  • Luke Lambourne
  • Yu Xia

Organizations

  • Boston University

Tags

DTIC Thesaurus Topics

  • Biology
  • Biomedical Engineering
  • Cells
  • Computational Biology
  • Data Sets
  • Engineering
  • Environment
  • Enzymes
  • Experimental Data
  • Fungi
  • Genes
  • Genetics
  • Metabolic Diseases
  • Metabolism
  • Systems Biology
  • United States
  • Virotherapy

Fields of Study

  • Biology

Readers

  • Economics
  • Mathematics or Statistics
  • Molecular Genetics