Department of Chemical and Systems Biology, Stanford University, Stanford, CA 94305, USA; Department of Developmental Biology, Stanford University, Stanford, CA 94305, USA; Institute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, CA 94305, USA; Howard Hughes Medical Institute, Stanford, CA 94305, USA.
Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Solna, Sweden.
Cell. 2024 Feb 1;187(3):692-711.e26. doi: 10.1016/j.cell.2023.12.032. Epub 2024 Jan 22.
Transcription factors (TFs) can define distinct cellular identities despite nearly identical DNA-binding specificities. One mechanism for achieving regulatory specificity is DNA-guided TF cooperativity. Although in vitro studies suggest that it may be common, examples of such cooperativity remain scarce in cellular contexts. Here, we demonstrate how "Coordinator," a long DNA motif composed of common motifs bound by many basic helix-loop-helix (bHLH) and homeodomain (HD) TFs, uniquely defines the regulatory regions of embryonic face and limb mesenchyme. Coordinator guides cooperative and selective binding between the bHLH family mesenchymal regulator TWIST1 and a collective of HD factors associated with regional identities in the face and limb. TWIST1 is required for HD binding and open chromatin at Coordinator sites, whereas HD factors stabilize TWIST1 occupancy at Coordinator and titrate it away from HD-independent sites. This cooperativity results in the shared regulation of genes involved in cell-type and positional identities and ultimately shapes facial morphology and evolution.
转录因子 (TFs) 尽管具有几乎相同的 DNA 结合特异性,但可以定义不同的细胞身份。实现调控特异性的一种机制是 DNA 指导的 TF 协同作用。尽管体外研究表明这种协同作用可能很常见,但在细胞环境中,这种协同作用的例子仍然很少。在这里,我们展示了“协调器”(一种由许多碱性螺旋-环-螺旋 (bHLH) 和同源域 (HD) TF 结合的常见基序组成的长 DNA 基序)如何独特地定义胚胎面部和肢体间充质的调控区域。协调器指导 TWIST1 等 bHLH 家族间充质调节因子与与面部和肢体区域身份相关的一系列 HD 因子之间的协同和选择性结合。TWIST1 对于 HD 结合和协调器位点的开放染色质是必需的,而 HD 因子稳定 TWIST1 在协调器上的占据,并将其从 HD 非依赖性位点上耗尽。这种协同作用导致参与细胞类型和位置身份的基因的共同调控,并最终塑造面部形态和进化。