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An intron based screen for functional innovation

Christian Schlötterer (ORCID: 0000-0003-4710-6526)
  • Grant DOI 10.55776/P19832
  • Funding program Principal Investigator Projects
  • Status ended
  • Start October 1, 2007
  • End December 31, 2011
  • Funding amount € 280,828
  • Project website

Disciplines

Biology (100%)

Keywords

  • Drosophila melanogaster,
  • Comparative genomics,
  • Selektion,
  • Intron
Abstract Final report

For long time, introns were considered to be evolving neutrally. Recently, this view has changed and it is widely recognized that many introns are conserved in length and sequence, which strongly supports their functional importance. This project aims to exploit the conservation of introns to perform a scan for functional innovation in Drosophila. Based on the availability of 12 fully sequenced Drosophila genomes, introns conserved in length or sequence will be identified. Among the functionally conserved introns, those will be identified that experienced a brief period of rapid change either in length or sequence. If this change is followed by a period of functional constraint these altered introns are regarded as indicators of a functional innovation. Using population genetics the functional conservation of candidate introns will be validated. A subset of the introns that experienced a putative functional innovation will be functionally tested using transgenesis and expression analyses.

For long time, introns were considered to be evolving neutrally. Recently, this view has changed and it is widely recognized that many introns are conserved in length and sequence, which strongly supports their functional importance. This project aims to exploit the conservation of introns to perform a scan for functional innovation in Drosophila. Based on the availability of 12 fully sequenced Drosophila genomes, introns conserved in length or sequence will be identified. Among the functionally conserved introns, those will be identified that experienced a brief period of rapid change either in length or sequence. If this change is followed by a period of functional constraint these altered introns are regarded as indicators of a functional innovation. Using population genetics the functional conservation of candidate introns will be validated. A subset of the introns that experienced a putative functional innovation will be functionally tested using transgenesis and expression analyses.

Research institution(s)
  • Veterinärmedizinische Universität Wien - 100%
International project participants
  • Bettina Harr, Max-Planck-Gesellschaft - Germany

Research Output

  • 636 Citations
  • 6 Publications
Publications
  • 2012
    Title Detecting Selective Sweeps from Pooled Next-Generation Sequencing Samples
    DOI 10.1093/molbev/mss090
    Type Journal Article
    Author Boitard S
    Journal Molecular Biology and Evolution
    Pages 2177-2186
    Link Publication
  • 2011
    Title The Genomic Signature of Splicing-Coupled Selection Differs between Long and Short Introns
    DOI 10.1093/molbev/msr201
    Type Journal Article
    Author Farlow A
    Journal Molecular Biology and Evolution
    Pages 21-24
    Link Publication
  • 2010
    Title Nonsense-Mediated Decay Enables Intron Gain in Drosophila
    DOI 10.1371/journal.pgen.1000819
    Type Journal Article
    Author Farlow A
    Journal PLoS Genetics
    Link Publication
  • 2010
    Title The Next Generation of Molecular Markers From Massively Parallel Sequencing of Pooled DNA Samples
    DOI 10.1534/genetics.110.114397
    Type Journal Article
    Author Futschik A
    Journal Genetics
    Pages 207-218
    Link Publication
  • 2010
    Title DNA double-strand break repair and the evolution of intron density
    DOI 10.1016/j.tig.2010.10.004
    Type Journal Article
    Author Farlow A
    Journal Trends in Genetics
    Pages 1-6
    Link Publication
  • 2009
    Title Expression profiling of Drosophila mitochondrial genes via deep mRNA sequencing
    DOI 10.1093/nar/gkp856
    Type Journal Article
    Author Torres T
    Journal Nucleic Acids Research
    Pages 7509-7518
    Link Publication

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+43 1 505 67 40

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