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Computational prediction of novel components of lung transcriptional networks

机译:肺转录网络新成分的计算预测

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摘要

Motivation: Little is known regarding the transcriptional mechanisms involved in forming and maintaining epithelial cell lineages of the mammalian respiratory tract. Results: Herein, a motif discovery approach was used to identify novel transcriptional regulators in the lung using genes previously found to be regulated by Foxa2 or Wnt signaling pathways. A human-mouse comparison of both novel and known motifs was also performed. Some of the factors and families identified here were previously shown to be involved epithelial cell differentiation (ETS family, HES-1 and MEIS-1), and ciliogenesis (RFX family), but have never been characterized in lung epithelia. Other unidentified over-represented motifs suggest the existence of novel mammalian lung transcription factors. Of the fraction of motifs examined we describe 25 transcription factor family predictions for lung. Fifteen novel factors were shown here to be expressed in mouse lung, and/or human bronchial or distal lung epithelial tissues or lung epithelial cell lineages.
机译:动机:关于形成和维持哺乳动物呼吸道上皮细胞谱系的转录机制知之甚少。结果:在本文中,使用一种基序发现方法,使用先前发现的受Foxa2或Wnt信号通路调节的基因,来鉴定肺中的新型转录调节因子。还进行了新颖和已知图案的人鼠比较。先前在此处确定的一些因素和家族已显示出与上皮细胞分化有关(ETS家族,HES-1和MEIS-1)和纤毛生成(RFX家族),但从未在肺上皮细胞中表征。其他无法确定的过度代表的主题暗示了新的哺乳动物肺转录因子的存在。在所检查的基序部分中,我们描述了25种针对肺的转录因子家族预测。此处显示了十五种新因子在小鼠肺和/或人支气管或远端肺上皮组织或肺上皮细胞谱系中表达。

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