促进器架构决定了基因表达的细胞间变异性
Daniel L Jones1, Robert C Brewster2, Rob Phillips3
1Department of Applied Physics, California Institute of Technology, Pasadena, CA 91125, USA.
概括
细胞基因表达的变异性是可以预测的. 转录的分子细节,而不仅仅是调节架构,控制这种变化,使转录噪声成为可调节的特征.
科学领域:
- 分子生物学分子生物学
- 系统生物学 系统生物学
- 遗传学 是一个遗传学.
背景情况:
- 基因表达的细胞间变异性是基因调节研究的一个关键领域.
- 在 prokaryotic 转录调节的理论模型和关于表达变异性的实验发现之间存在差距.
- 现有研究表明,可变性独立于调节架构,与一些分子模型相矛盾.
研究的目的:
- 研究Escherichia coli中转录和基因表达变异性的分子细节之间的关系.
- 为了确定基因表达变异性是否受到促进体强度,转录因子结合和转录因子拷贝数的影响.
- 测试无参数模型是否可以预测观察到的基因表达变异性.
主要方法:
- 以不同强度和转录因子结合特征的大肠杆菌促进体的系统构造.
- 使用信使RNA (mRNA) 光在位杂交来量化基因表达变异性.
- 将实验数据与来自无参数分子模型的预测进行比较.
主要成果:
- 发现基因表达的变异性取决于转录的分子细节.
- 促进体和转录因子参数的系统变化直接影响了mRNA表达的可变性.
- 无参数模型准确预测了实验观察到的基因表达的变异性.
结论:
- 控制转录的分子机制直接决定mRNA表达的变异性.
- 转录噪声是一种可调的参数,这表明它可以通过进化过程来塑造.
- 基因表达的变异性与底层的调节架构并非无关,而是通过转录细节精确控制.
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