Epigenetically regulated genomic expressions for shortened stature and cleft palate are regionally specific in the 11-day mouse embryo.

M N Runner
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Abstract

Chronokinetic synergism, a holistic and extremely sensitive experimental design, has shown in the mouse embryo that site-specific epigenetic forces differentially regulate genesis of the palate (cleft palate) and limb bud organogenesis (shortened stature). Acute exposures of 11-day pregnant mice to minimally effective doses of thymidine or ethanol followed 5 or 8 hr later by minimal exposure to retinoic acid have enabled quantitative and qualitative assay for genomic-epigenetic interactions. These site-specific morphogenetic regulations occurred during palatal genesis from the maxillary prominence of the first pharyngeal arch and during limb bud prechondrogenesis. Thymidine is presumed to induce its response by inhibition of DNA polymerase and hence by transitory cytostatic block. (Embryo size was not detectably changed). Ethanol is interpreted, guilt by associated response, indirectly to interfere with histone regulation of transcription. Two central findings have demonstrated the coordinated regulation of genomic and epigenetic positional information. First, thymidine or ethanol as epigenetic probes for limb prechondrogenesis and palatal precursor cells have activated distinctive site-specific responses. Second, responses to chronokinetic synergisms have indicated that epigenetic regulators for limb and palate dysmorphogenesis may affect distinctly different phases of the cell division cycle and hence induce differential DNA expressions. Although each of palate and limb is concurrently susceptible to epigenetic regulation, their differential intrinsic genomic capabilities appear to have been uncoupled. The putative homeostatic balance of genomic expressions in the palate precursor and the prechondrogenic limb bud cells of the 11-day mouse embryo has been characterized as epigenetically regulated, alternatively expressed, and positionally restricted. We propose that the chronokinetic synergisms have disclosed the existence of distinctive palate-determining genes and stature-determining genes.

在11天的小鼠胚胎中,表观遗传调控的身高缩短和腭裂的基因组表达具有区域特异性。
时间动力学协同作用,一个整体的和极其敏感的实验设计,已经在小鼠胚胎中显示了位点特异性表观遗传力差异调节腭(腭裂)和肢体芽器官发生(身材缩短)。将怀孕11天的小鼠急性暴露于最低有效剂量的胸腺嘧啶或乙醇中,5或8小时后再暴露于最低剂量的维甲酸中,可以对基因组-表观遗传相互作用进行定量和定性分析。这些特定部位的形态发生调控发生在第一咽弓上颌突腭发生和肢芽软骨前形成期间。胸腺嘧啶被认为是通过抑制DNA聚合酶和短暂的细胞抑制剂阻断来诱导其反应的。(胚胎大小未见明显变化)。乙醇通过相关反应被解读,间接干扰组蛋白的转录调节。两个中心发现已经证明了基因组和表观遗传位置信息的协调调节。首先,胸苷嘧啶或乙醇作为肢体软骨前体细胞和腭前体细胞的表观遗传探针,激活了独特的位点特异性反应。其次,对时间动力学协同作用的响应表明,肢体和腭畸形发生的表观遗传调控因子可能影响细胞分裂周期的不同阶段,从而诱导差异的DNA表达。尽管上颚和肢体同时受表观遗传调控的影响,但它们内在的差异基因组能力似乎是不耦合的。在11天小鼠胚胎的上颚前体和软骨前体细胞中,基因组表达的稳态平衡被描述为表观遗传调控、交替表达和位置限制。我们认为,时间动力学协同作用揭示了独特的味觉决定基因和身高决定基因的存在。
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