The 3' region of the ZPA regulatory sequence (ZRS) is required for activity and contains a critical E-box.

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2025-07-02 eCollection Date: 2025-01-01 DOI:10.3389/fcell.2025.1569573
Kathryn F Ball, Stephen Manu, Abbie K Underhill, Jeanyoung Kim, Jessica C Britton, Sarah R Rudd, Madison M Malone, Japhet Amoah, Allen Cooper, Charmaine Pira, Kerby C Oberg
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引用次数: 0

Abstract

Background: 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 in vitro. 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.

Methods: 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 in vivo chicken limb bioassay. We validated our findings using select ZRS constructs in transgenic mice.

Results: 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.

Conclusion: 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.

ZPA调控序列(ZRS)的3'区是活性所必需的,并且包含一个关键的E-box。
背景:在发育过程中,Hand2和Hoxd13转录因子(TFs)在后肢远端中胚层极化活性区(ZPA)调节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,控制Shh的表达。ZRS可分为5‘,中心和3’子域,每个子域都有一个E-box位点,可以结合基本的螺旋-环-螺旋(bHLH) tf,如Hand2。此外,两个Hoxd13位点存在于5'和中心子域。据称,Hand2通过中心E-box结合ZRS,并且Hand2和Hoxd13已被证明在体外激活ZRS。我们假设活动需要中央E-box,而其他E-box和Hoxd13位点将ZRS活动定位于远端后肢中胚层。方法:为了确定每个子域的功能作用,我们生成了三个ZRS片段(5‘,中心和3’),并结合片段构建来测试子域的集体贡献。此外,我们使用位点定向诱变单独或协同破坏了五个结合位点。所有的ZRS构建体都被克隆到GFP报告基因中,并在鸡肢体体内生物测定中进行了评价。我们在转基因小鼠中使用选择的ZRS构建物验证了我们的发现。结果:我们发现3‘片段是ZRS活性所必需的,而5’和中心片段单独或联合不具有活性。然而,将3‘片段与5’片段结合可以恢复强健的活性。此外,所有五个结合位点的突变都显著降低了ZRS的活性。恢复每个Hoxd13位点可以恢复病灶活动,而恢复5'和中央e -box的作用很小。然而,即使在没有其他四个结合位点的情况下,3' E-box也被证明具有足够的活性。结论:我们的数据表明,ZRS 3‘而不是中央子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-box,而5'和中央E-box似乎具有抑制性。我们的数据还表明Hoxd13结合位点促进了ZPA内的局部活性。
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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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