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Functional overlap and regulatory links shape genetic interactions between signaling pathways

机译:功能重叠和调节联系决定了信号通路之间的遗传相互作用

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To understand relationships between phosphorylation-based signaling pathways, we analyzed 150 deletion mutants of protein kinases and phosphatases in S. cerevisiae using DNA microarrays. Downstream changes in gene expression were treated as a phenotypic readout. Double mutants with synthetic genetic interactions were included to investigate genetic buffering relationships such as redundancy. Three types of genetic buffering relationships are identified: mixed epistasis, complete redundancy, and quantitative redundancy. In mixed epistasis, the most common buffering relationship, different gene sets respond in different epistatic ways. Mixed epistasis arises from pairs of regulators that have only partial overlap in function and that are coupled by additional regulatory links such as repression of one by the other. Such regulatory modules confer the ability to control different combinations of processes depending on condition or context. These properties likely contribute to the evolutionary maintenance of paralogs and indicate a way in which signaling pathways connect for multiprocess control.
机译:为了解基于磷酸化的信号通路之间的关系,我们使用DNA微阵列分析了酿酒酵母中150种蛋白激酶和磷酸酶的缺失突变体。基因表达的下游变化被视为表型读数。包括具有合成遗传相互作用的双突变体以研究遗传缓冲关系,例如冗余。确定了三种类型的遗传缓冲关系:混合上位,完全冗余和定量冗余。在最常见的缓冲关系混合上皮中,不同的基因组以不同的上皮方式反应。混合上位性源自成对的调节剂,它们在功能上仅部分重叠,并通过其他调节环节(例如彼此抑制)联系在一起。这种调节模块赋予了根据条件或环境控制不同过程组合的能力。这些特性可能有助于旁系同源物的进化维持,并指示信号通路连接以进行多过程控制的方式。

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