同源结构域转录因子Msx-2调控子宫祖细胞对己烯雌酚的应答。

Yan Yin, Congxing Lin, Ivy Zhang, Alexander V Fisher, Maulik Dhandha, Liang Ma
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引用次数: 2

摘要

小鼠子宫上皮祖细胞的命运在出生后5 - 7天确定。在这个关键的时间窗口,暴露于内分泌干扰物己烯雌酚(DES)可以深刻地改变子宫细胞分化。我们之前已经证明同源结构域转录因子MSX-2在女性生殖道(FRT)的des反应性中起重要作用。突变型FRTs在用DES治疗时表现出更严重的表型,并伴有依赖于Msx2的基因表达变化。为了更好地了解MSX-2在子宫对DES反应中的作用,我们在缺乏Msx2的小鼠中进行了全球基因表达谱实验,并将这一结果与我们之前发表的野生型小鼠的微阵列数据进行了比较,我们提取了两种基因型中的共同和差异调控基因。通过这样做,我们确定了MSX-2的潜在下游靶点,以及DES通过MSX-2调节的基因。这些基因的发现将有助于更好地理解DES以及其他内分泌干扰物是如何影响生殖器官发育的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Homeodomain Transcription Factor Msx-2 Regulates Uterine Progenitor Cell Response to Diethylstilbestrol.

Homeodomain Transcription Factor Msx-2 Regulates Uterine Progenitor Cell Response to Diethylstilbestrol.

Homeodomain Transcription Factor Msx-2 Regulates Uterine Progenitor Cell Response to Diethylstilbestrol.

Homeodomain Transcription Factor Msx-2 Regulates Uterine Progenitor Cell Response to Diethylstilbestrol.

The fate of mouse uterine epithelial progenitor cells is determined between postnatal days 5 to 7. Around this critical time window, exposure to an endocrine disruptor, diethylstilbestrol (DES), can profoundly alter uterine cytodifferentiation. We have shown previously that a homeo domain transcription factor MSX-2 plays an important role in DES-responsiveness in the female reproductive tract (FRT). Mutant FRTs exhibited a much more severe phenotype when treated with DES, accompanied by gene expression changes that are dependent on Msx2. To better understand the role that MSX-2 plays in uterine response to DES, we performed global gene expression profiling experiment in mice lacking Msx2 By comparing this result to our previously published microarray data performed on wild-type mice, we extracted common and differentially regulated genes in the two genotypes. In so doing, we identified potential downstream targets of MSX-2, as well as genes whose regulation by DES is modulated through MSX-2. Discovery of these genes will lead to a better understanding of how DES, and possibly other endocrine disruptors, affects reproductive organ development.

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