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Transcription Factor Binding Site Analysis Identifies FOXO Transcription Factors as Regulators of the Cutaneous Wound Healing Process.

机译:转录因子结合位点分析将FOXO转录因子识别为皮肤伤口愈合过程的调节因子。

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摘要

The search for significantly overrepresented and co-occurring transcription factor binding sites in the promoter regions of the most differentially expressed genes in microarray data sets could be a powerful approach for finding key regulators of complex biological processes. To test this concept, two previously published independent data sets on wounded human epidermis were re-analyzed. The presence of co-occurring transcription factor binding sites for FOXO1, FOXO3 and FOXO4 in the majority of the promoter regions of the most significantly differentially expressed genes between non-wounded and wounded epidermis implied an important role for FOXO transcription factors during wound healing. Expression levels of FOXO transcription factors during wound healing in vivo in both human and mouse skin were analyzed and a decrease for all FOXOs in human wounded skin was observed, with FOXO3 having the highest expression level in non wounded skin. Impaired re-epithelialization was found in cultures of primary human keratinocytes expressing a constitutively active variant of FOXO3. Conversely knockdown of FOXO3 in keratinocytes had the opposite effect and in an in vivo mouse model with FOXO3 knockout mice we detected significantly accelerated wound healing. This article illustrates that the proposed approach is a viable method for identifying important regulators of complex biological processes using in vivo samples. FOXO3 has not previously been implicated as an important regulator of wound healing and its exact function in this process calls for further investigation.
机译:在微阵列数据集中最差异表达的基因的启动子区域中寻找明显过量表达且同时存在的转录因子结合位点,可能是寻找复杂生物过程关键调控因子的有效方法。为了验证这一概念,重新分析了两个先前公布的有关受伤人表皮的独立数据集。在未受伤和受伤表皮之间表达最显着差异的基因的大多数启动子区域中,FOXO1,FOXO3和FOXO4共同存在的转录因子结合位点的存在暗示了FOXO转录因子在伤口愈合过程中的重要作用。分析了人类和小鼠皮肤在体内伤口愈合过程中FOXO转录因子的表达水平,并观察到人类受伤皮肤中所有FOXO的减少,其中FOXO3在非伤口皮肤中的表达水平最高。在表达FOXO3组成型活性变体的原代人角质形成细胞的培养物中发现受损的上皮再生。相反,在角质形成细胞中敲低FOXO3具有相反的效果,在具有FOXO3敲除小鼠的体内小鼠模型中,我们检测到伤口愈合明显加快。本文说明,提出的方法是一种使用体内样品鉴定复杂生物过程的重要调节剂的可行方法。 FOXO3以前尚未被认为是伤口愈合的重要调节剂,其在此过程中的确切功能需要进一步研究。

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