多梳蛋白复合物与GATA-6/PPARα相互作用抑制α-MHC表达。

IF 1.7 4区 生物学 Q4 CELL BIOLOGY Development Growth & Differentiation Pub Date : 2024-12-26 DOI:10.1111/dgd.12953
Fei-Fei Dai, Jing Chen, Zhen Ma, Ming-Hui Yang, Tong Sun, Juan Ma, Meng-Jiao Zhou, Zhi-Ru Wei, Yunzeng Zou, Shoutao Zhang, Ming-Xi Zang
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引用次数: 0

摘要

转录因子与表观遗传调控因子协同协调心脏分化以促进心脏发育,但其潜在机制尚不完全清楚。在这里,我们报道了GATA-6诱导心脏分化,但过氧化物酶体增殖物激活受体α (PPARα)逆转了GATA-6诱导的心脏分化,可能是因为GATA-6/PPARα将含有EZH2/Ring1b/BMI1的多梳子蛋白复合物募集到心脏特异性α-肌球蛋白重链(α- mhc)基因的启动子上,抑制α- mhc的表达,最终抑制心脏分化。此外,Ring1b泛素化PPARα和GATA-6。通过过表达和敲除EZH2/BMI1,证实了多梳蛋白复合物抑制GATA-6和PPARα诱导的心脏分化。总之,我们的研究结果表明,多梳蛋白复合物与GATA-6/PPARα相互作用抑制心脏分化,这一发现可能促进先天性心脏病新疗法的发展。
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The polycomb protein complex interacts with GATA-6/PPARα to inhibit α-MHC expression

Transcription factors collaborate with epigenetic regulatory factors to orchestrate cardiac differentiation for heart development, but the underlying mechanism is not fully understood. Here, we report that GATA-6 induces cardiac differentiation but peroxisome proliferator-activated receptor α (PPARα) reverses GATA-6-induced cardiac differentiation, possibly because GATA-6/PPARα recruits the polycomb protein complex containing EZH2/Ring1b/BMI1 to the promoter of the cardiac-specific α-myosin heavy chain (α-MHC) gene and suppresses α-MHC expression, which ultimately inhibits cardiac differentiation. Furthermore, Ring1b ubiquitylates PPARα and GATA-6. By overexpression and knockout of EZH2/BMI1, it was demonstrated that the polycomb protein complex inhibits cardiac differentiation induced by GATA-6 and PPARα. Together, our results demonstrate that the polycomb protein complex interacts with GATA-6/PPARα to inhibit cardiac differentiation, a finding that could facilitate the development of new therapies for congenital heart disease.

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来源期刊
Development Growth & Differentiation
Development Growth & Differentiation 生物-发育生物学
CiteScore
4.60
自引率
4.00%
发文量
62
审稿时长
6 months
期刊介绍: Development Growth & Differentiation (DGD) publishes three types of articles: original, resource, and review papers. Original papers are on any subjects having a context in development, growth, and differentiation processes in animals, plants, and microorganisms, dealing with molecular, genetic, cellular and organismal phenomena including metamorphosis and regeneration, while using experimental, theoretical, and bioinformatic approaches. Papers on other related fields are also welcome, such as stem cell biology, genomics, neuroscience, Evodevo, Ecodevo, and medical science as well as related methodology (new or revised techniques) and bioresources. Resource papers describe a dataset, such as whole genome sequences and expressed sequence tags (ESTs), with some biological insights, which should be valuable for studying the subjects as mentioned above. Submission of review papers is also encouraged, especially those providing a new scope based on the authors’ own study, or a summarization of their study series.
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