4.8 Article

miR-9a Minimizes the Phenotypic Impact of Genomic Diversity by Buffering a Transcription Factor

Journal

CELL
Volume 155, Issue 7, Pages 1556-1567

Publisher

CELL PRESS
DOI: 10.1016/j.cell.2013.10.057

Keywords

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Funding

  1. Chicago Biomedical Consortium
  2. Malkin Foundation
  3. Rappaport Foundation
  4. Pew Latin American Fellows Program
  5. McNair Medical Institute
  6. Howard Hughes Medical Institute
  7. NIH [T32GM008061, T32 HL094282, P50 GM81892, T32 GM007526, GM068743, GM077581]

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Gene expression has to withstand stochastic, environmental, and genomic perturbations. For example, in the latter case, 0.5%-1% of the human genome is typically variable between any two unrelated individuals. Such diversity might create problematic variability in the activity of gene regulatory networks and, ultimately, in cell behaviors. Using multigenerational selection experiments, we find that for the Drosophila proneural network, the effect of genomic diversity is dampened by miR-9a-mediated regulation of senseless expression. Reducing miR-9a regulation of the Senseless transcription factor frees the genomic landscape to exert greater phenotypic influence. Whole-genome sequencing identified genomic loci that potentially exert such effects. A larger set of sequence variants, including variants within proneural network genes, exhibits these characteristics when miR-9a concentration is reduced. These findings reveal that microRNA-target interactions may be a key mechanism by which the impact of genomic diversity on cell behavior is dampened.

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