Ball Kathryn F, Manu Stephen, Underhill Abbie K, Kim Jeanyoung, Britton Jessica C, Rudd Sarah R, Malone Madison M, Amoah Japhet, Cooper Allen, Pira Charmaine, Oberg Kerby C
Pathology and Human Anatomy Department, Loma Linda University, Loma Linda, CA, United States.
Basic Sciences Department, Loma Linda University, Loma Linda, CA, United States.
Front Cell Dev Biol. 2025 Jul 2;13:1569573. doi: 10.3389/fcell.2025.1569573. eCollection 2025.
During development, Hand2 and Hoxd13 transcription factors (TFs) regulate Sonic hedgehog (Shh) expression in the zone of polarizing activity (ZPA) in the distal posterior limb mesoderm. The ZPA regulatory sequence (ZRS) is a conserved, limb-specific enhancer that controls Shh expression. The ZRS can be divided into 5', central, and 3' subdomains, each with an E-box site that can bind basic helix-loop-helix (bHLH) TFs like Hand2. In addition, two Hoxd13 sites are present in the 5' and central subdomains. Hand2 purportedly binds the ZRS through the central E-box, and both Hand2 and Hoxd13 have been shown to activate the ZRS . We hypothesized that the central E-box was required for activity, while the other E-boxes and Hoxd13 sites localize ZRS activity to the distal posterior limb mesoderm.
To identify the functional role of each subdomain, we generated three ZRS fragments (5', central, and 3') and combined fragment constructs to test subdomain collective contributions. Additionally, we disrupted the five binding sites, alone or in concert, using site-directed mutagenesis. All ZRS constructs were cloned into a GFP reporter and evaluated in an chicken limb bioassay. We validated our findings using select ZRS constructs in transgenic mice.
We found that the 3' fragment was necessary for ZRS activity, while the 5' and central fragments had no activity alone or when combined. However, combining the 3' fragment with the 5' fragment restored robust activity. Further, mutation of all five binding sites markedly reduced ZRS activity. Reinstating each of the Hoxd13 sites restored focal activity, while restoring the 5' and central E-boxes had little effect. However, the 3' E-box proved sufficient for robust activity even in the absence of the other four binding sites.
Our data indicate that the ZRS 3', not the central, subdomain is necessary for activity and contains the 3' E-box that Hand2 likely uses to induce Shh expression, while the 5' and central E-boxes appear to be inhibitory. Our data also suggest that the Hoxd13 binding sites promote localized activity within the ZPA.
在发育过程中,Hand2和Hoxd13转录因子(TFs)调节后肢远端中胚层极化活性区(ZPA)中 Sonic hedgehog(Shh)的表达。ZPA调控序列(ZRS)是一个保守的、肢体特异性增强子,可控制Shh的表达。ZRS可分为5'、中央和3'亚结构域,每个亚结构域都有一个E盒位点,可结合像Hand2这样的碱性螺旋-环-螺旋(bHLH)转录因子。此外,5'和中央亚结构域中存在两个Hoxd13位点。据称,Hand2通过中央E盒与ZRS结合,并且Hand2和Hoxd13均已被证明可激活ZRS。我们假设中央E盒是活性所必需的,而其他E盒和Hoxd13位点将ZRS活性定位于后肢远端中胚层。
为了确定每个亚结构域的功能作用,我们生成了三个ZRS片段(5'、中央和3'),并组合片段构建体以测试亚结构域的集体贡献。此外,我们使用定点诱变单独或协同破坏五个结合位点。所有ZRS构建体均克隆到GFP报告基因中,并在鸡肢体生物测定中进行评估。我们使用转基因小鼠中的选定ZRS构建体验证了我们的发现。
我们发现3'片段是ZRS活性所必需的,而5'和中央片段单独或组合时均无活性。然而,将3'片段与5'片段组合可恢复强大的活性。此外,所有五个结合位点的突变均显著降低了ZRS活性。恢复每个Hoxd13位点可恢复局部活性,而恢复5'和中央E盒影响不大。然而,即使在没有其他四个结合位点的情况下,3'E盒也足以产生强大的活性。
我们的数据表明,ZRS的3'亚结构域而非中央亚结构域是活性所必需的,并且包含Hand2可能用于诱导Shh表达的3'E盒,而5'和中央E盒似乎具有抑制作用。我们的数据还表明,Hoxd13结合位点促进了ZPA内的局部活性。