bHLH-PAS蛋白对果蝇尾侧同源盒基因的转录调控

Yoon-Jeong Choi , Eun-Jeong Kwon , Joung-Sun Park , Ho-Sung Kang , Young-Shin Kim , Mi-Ae Yoo
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引用次数: 3

摘要

尾侧同源盒转录因子参与了前后轴的定义和肠道发育。最近的报道表明,CDX1和CDX2(尾果蝇的人类同源基因)的失调与几种类型的癌症有关。然而,对指导尾侧同源盒基因表达的调控机制知之甚少。在这项研究中,我们已经确定了bHLH-PAS蛋白的结合位点,称为CNS中线元件(CME),位于果蝇尾部基因的5 ' -侧翼区域。对携带携带野生型或突变型CME的尾侧- lacz融合基因的转基因果蝇的分析表明,CME位点是尾侧基因在体内表达所必需的。我们还确定尾端启动子活性可以通过CME位点被Trachealess (Trh)/Tango (Tgo) bHLH-PAS蛋白调节。我们的研究结果表明,果蝇尾部基因是Trh/Tgo bHLH-PAS蛋白的靶标。
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Transcriptional regulation of the Drosophila caudal homeobox gene by bHLH–PAS proteins

Caudal-related homeobox transcription factors are involved in the definition of the anteroposterior axis and intestinal development. Recent reports indicate that dysregulation of CDX1 and CDX2, the human homologues of Drosophila caudal, are associated with several types of cancer. Very little is known, however, about the regulatory mechanisms that direct the caudal-related homeobox gene expression. In this study, we have identified the binding sites for bHLH–PAS proteins, referred to as CNS midline element (CME), in the 5′-flanking region of the Drosophila caudal gene. Analyses using transgenic flies carrying a caudal-lacZ fusion gene bearing a wild-type or mutant CME indicate that the CME sites are required for caudal gene expression in vivo. We also determined that the caudal promoter activity can be regulated by Trachealess (Trh)/Tango (Tgo) bHLH–PAS proteins, via the CME sites. Our results suggest that the Drosophila caudal gene is a target of the Trh/Tgo bHLH–PAS proteins.

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