miR-9a Minimizes the Phenotypic Impact of Genomic Diversity by Buffering a Transcription Factor
Author(s) -
Justin J. Cassidy,
Aashish R. Jha,
Diana M. Posadas,
Ritika Giri,
Koen J. T. Venken,
Jingran Ji,
Hongmei Jiang,
Hugo J. Bellen,
K White,
Richard W. Carthew
Publication year - 2013
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2013.10.057
Subject(s) - biology , transcription factor , phenotype , genetics , diversity (politics) , computational biology , transcription (linguistics) , evolutionary biology , gene , linguistics , philosophy , sociology , anthropology
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.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom