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Multi-level and lineage-specific interactomes of the Hox transcription factor Ubx contribute to its functional specificity

机译:HOX转录因子UBX的多级和谱系特异性副间对其功能特异性有助于

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Transcription factors (TFs) control cell fates by precisely orchestrating gene expression. However, how individual TFs promote transcriptional diversity remains unclear. Here, we use the Hox TF Ultrabithorax (Ubx) as a model to explore how a single TF specifies multiple cell types. Using proximity-dependent Biotin IDentification in Drosophila , we identify Ubx interactomes in three embryonic tissues. We find that Ubx interacts with largely non-overlapping sets of proteins with few having tissue-specific RNA expression. Instead most interactors are active in many cell types, controlling gene expression from chromatin regulation to the initiation of translation. Genetic interaction assays in vivo confirm that they act strictly lineage- and process-specific. Thus, functional specificity of Ubx seems to play out at several regulatory levels and to result from the controlled restriction of the interaction potential by the cellular environment. Thereby, it challenges long-standing assumptions such as differential RNA expression as determinant for protein complexes.
机译:通过精确协调基因表达,转录因子(TFS)控制细胞命名。但是,单个TFS如何促进转录分类仍然尚不清楚。在这里,我们使用Hox TF Ultrabithorax(UBX)作为模型来探索单个TF如何指定多个单元格类型。在果蝇中使用邻近依赖的生物素鉴定,我们鉴定了三种胚胎组织中的UBX椎间膜。我们发现UBX与很大程度上的非重叠蛋白质相互作用,少数具有组织特异性的RNA表达。相反,大多数交互式在许多细胞类型中是活性的,控制从染色质调节的基因表达到翻译的开始。体内遗传相互作用测定证实,它们是严格的血统和过程特定的。因此,UBX的功能特异性似乎在若干调节水平下发挥作用,并且由细胞环境受相互作用电位的受控限制来发挥作用。因此,它挑战了诸如蛋白质复合物的差分RNA表达的长期假设,例如蛋白质复合物的决定因素。

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