Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, Massachusetts.
Dev Dyn. 2014 Jan;243(1):4-15. doi: 10.1002/dvdy.23997. Epub 2013 Jul 22.
Hox genes encode transcription factors with important roles during embryogenesis and tissue differentiation. Genetic analyses initially demonstrated that interfering with Hox genes has profound effects on the specification of cell identity, suggesting that Hox proteins regulate very specific sets of target genes. However, subsequent biochemical analyses revealed that Hox proteins bind DNA with relatively low affinity and specificity. Furthermore, it became clear that a given Hox protein could activate or repress transcription, depending on the context. A resolution to these paradoxes presented itself with the discovery that Hox proteins do not function in isolation, but interact with other factors in complexes. The first such "cofactors" were members of the Extradenticle/Pbx and Homothorax/Meis/Prep families. However, the list of Hox-interacting proteins has continued to grow, suggesting that Hox complexes contain many more components than initially thought. Additionally, the activities of the various components and the exact mechanisms whereby they modulate the activity of the complex remain puzzling. Here, we review the various proteins known to participate in Hox complexes and discuss their likely functions. We also consider that Hox complexes of different compositions may have different activities and discuss mechanisms whereby Hox complexes may be switched between active and inactive states.
Hox 基因编码在胚胎发生和组织分化过程中具有重要作用的转录因子。遗传分析最初表明,干扰 Hox 基因对细胞身份的特化具有深远影响,这表明 Hox 蛋白调节非常特定的靶基因集。然而,随后的生化分析表明,Hox 蛋白与 DNA 的结合亲和力和特异性相对较低。此外,越来越明显的是,给定的 Hox 蛋白可以根据上下文激活或抑制转录。随着发现 Hox 蛋白不是孤立起作用,而是与复合物中的其他因素相互作用,这些悖论得到了解决。第一个这样的“共因子”是 Extradenticle/Pbx 和 Homothorax/Meis/Prep 家族的成员。然而,与 Hox 相互作用的蛋白质列表仍在继续增加,这表明 Hox 复合物包含的成分比最初想象的要多。此外,各种成分的活性以及它们调节复合物活性的确切机制仍然令人费解。在这里,我们回顾了已知参与 Hox 复合物的各种蛋白质,并讨论了它们可能的功能。我们还认为,不同组成的 Hox 复合物可能具有不同的活性,并讨论了 Hox 复合物如何在激活和非激活状态之间切换的机制。