Department of Genetics and Evolution, University of Geneva, Geneva, Switzerland.
Institut NeuroMyoGène, CNRS UMR 5310, INSERM U1217, University Claude Bernard Lyon1, Lyon, France.
Dev Dyn. 2021 Sep;250(9):1280-1299. doi: 10.1002/dvdy.303. Epub 2021 Mar 1.
During tetrapod limb development, the HOXA13 and HOXD13 transcription factors are critical for the emergence and organization of the autopod, the most distal aspect where digits will develop. Since previous work had suggested that the Dbx2 gene is a target of these factors, we set up to analyze in detail this potential regulatory interaction.
We show that HOX13 proteins bind to mammalian-specific sequences at the vicinity of the Dbx2 locus that have enhancer activity in developing digits. However, the functional inactivation of the DBX2 protein did not elicit any particular phenotype related to Hox genes inactivation in digits, suggesting either redundant or compensatory mechanisms. We report that the neighboring Nell2 and Ano6 genes are also expressed in distal limb buds and are in part controlled by the same Dbx2 enhancers despite being localized into two different topologically associating domains (TADs) flanking the Dbx2 locus.
We conclude that Hoxa13 and Hoxd genes cooperatively activate Dbx2 expression in developing digits through binding to mammalian specific regulatory sequences in the Dbx2 neighborhood. Furthermore, these enhancers can overcome TAD boundaries in either direction to co-regulate a set of genes located in distinct chromatin domains.
在四足动物肢体发育过程中,HOXA13 和 HOXD13 转录因子对于指节的出现和组织形成至关重要,指节是最远端的部位,将发育出手指。由于之前的工作表明 Dbx2 基因是这些因子的一个靶点,我们着手详细分析这种潜在的调控相互作用。
我们表明 HOX13 蛋白与 Dbx2 基因座附近的哺乳动物特异性序列结合,这些序列在发育中的指节中具有增强子活性。然而,DBX2 蛋白的功能失活并没有引起与 Hox 基因失活相关的任何特定的手指表型,这表明存在冗余或补偿机制。我们报告说,相邻的 Nell2 和 Ano6 基因也在远端肢芽中表达,并且部分受到相同的 Dbx2 增强子的控制,尽管它们被定位在 Dbx2 基因座两侧的两个不同的拓扑关联域 (TAD) 中。
我们得出结论,Hoxa13 和 Hoxd 基因通过与 Dbx2 基因座附近的哺乳动物特异性调节序列结合,在发育中的指节中协同激活 Dbx2 的表达。此外,这些增强子可以克服任意方向的 TAD 边界,共同调节位于不同染色质域的一组基因。