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

机译:miR-9a通过缓冲转录因子使基因组多样性的表型影响最小化

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摘要

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 regu lation 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.
机译:基因表达必须承受随机的,环境的和基因组的干扰。例如,在后一种情况下,人类基因组的0.5%-1%通常在任意两个不相关的个​​体之间可变。这种多样性可能会在基因调控网络的活动中以及最终在细胞行为中造成问题性的可变性。使用多代选择实验,我们发现对于果蝇的神经网络,miR-9a介导的无意义表达调节基因组多样性的作用。减少无意义转录因子的miR-9a调控可释放基因组格局,以发挥更大的表型影响。全基因组测序确定了可能发挥这种作用的基因组位点。当miR-9a浓度降低时,较大的一组序列变体,包括前神经网络基因内的变体,表现出这些特征。这些发现表明,microRNA-靶标相互作用可能是抑制基因组多样性对细胞行为影响的关键机制。

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