Genes targeted by the Hedgehog-signaling pathway can be regulated by Estrogen related receptor β

IF 2.946 Q3 Biochemistry, Genetics and Molecular Biology BMC Molecular Biology Pub Date : 2015-11-23 DOI:10.1186/s12867-015-0047-3
Yuan Lu, Jilong Li, Jianlin Cheng, Dennis B. Lubahn
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引用次数: 20

Abstract

Nuclear receptor family member, Estrogen related receptor β, and the Hedgehog signal transduction pathway are both reported to relate to tumorigenesis and induced pluripotent stem cell reprogramming. We hypothesize that Estrogen related receptor β can modulate the Hedgehog signaling pathway and affect Hedgehog driven downstream gene expression.

We established an estrogen related receptor β-expressing Hedgehog-responsive NIH3T3 cell line by Esrrb transfection, and performed mRNA profiling using RNA-Seq after Hedgehog ligand conditioned medium treatment. Esrrb expression altered 171 genes, while Hedgehog signaling activation alone altered 339 genes. Additionally, estrogen related receptor β expression in combination with Hedgehog signaling activation affects a group of 109 Hedgehog responsive mRNAs, including Hsd11b1, Ogn, Smoc2, Igf1, Pdcd4, Igfbp4, Stmn1, Hp, Hoxd8, Top2a, Tubb4b, Sfrp2, Saa3, Prl2c3 and Dpt.

We conclude that Estrogen related receptor β is capable of interacting with Hh-signaling downstream targets. Our results suggest a new level of regulation of Hedgehog signaling by Estrogen related receptor β, and indicate modulation of Estrogen related receptor β can be a new strategy to regulate various functions driven by the Hedgehog signaling pathway.

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hedgehog -信号通路的靶基因可受雌激素相关受体β的调控
据报道,核受体家族成员、雌激素相关受体β和Hedgehog信号转导通路都与肿瘤发生和诱导多能干细胞重编程有关。我们推测雌激素相关受体β可以调节Hedgehog信号通路并影响Hedgehog驱动的下游基因表达。我们通过Esrrb转染建立了表达雌激素相关受体β的刺猬应答性NIH3T3细胞株,并在Hedgehog配体条件培养基处理后使用RNA-Seq进行mRNA谱分析。Esrrb表达改变了171个基因,而Hedgehog信号激活单独改变了339个基因。此外,雌激素相关受体β表达与Hedgehog信号激活联合影响一组109个Hedgehog应答mrna,包括Hsd11b1、Ogn、Smoc2、Igf1、Pdcd4、Igfbp4、Stmn1、Hp、Hoxd8、Top2a、Tubb4b、Sfrp2、Saa3、Prl2c3和Dpt。我们得出结论,雌激素相关受体β能够与hh信号下游靶点相互作用。我们的研究结果提示了雌激素相关受体β对Hedgehog信号通路的调控达到了一个新的水平,并且表明雌激素相关受体β的调控可能是调控Hedgehog信号通路驱动的各种功能的新策略。
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来源期刊
BMC Molecular Biology
BMC Molecular Biology 生物-生化与分子生物学
CiteScore
4.80
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: BMC Molecular Biology is an open access journal publishing original peer-reviewed research articles in all aspects of DNA and RNA in a cellular context, encompassing investigations of chromatin, replication, recombination, mutation, repair, transcription, translation and RNA processing and function.
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