YTHDF1 是维持心脏稳态的关键。

IF 4.9 2区 医学 Q1 CARDIAC & CARDIOVASCULAR SYSTEMS
Volha A. Golubeva , Anindhya Sundar Das , Charles P. Rabolli , Lisa E. Dorn , Jop H. van Berlo , Federica Accornero
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引用次数: 0

摘要

RNA结合蛋白YTH-domain家族(YTHDF)可通过调节具有N6-甲基腺苷(m6A)修饰的mRNA,在转录后水平控制基因表达。尽管已确定 m6A 在心脏中的重要性,但特定 m6A 结合蛋白在心脏中的作用仍不清楚。在这里,我们利用新产生的心脏受限小鼠模型鉴定了 YTHDF1 在心肌细胞中的功能。在成年心肌细胞中缺失 YTHDF1 会导致肥大、纤维化和功能障碍。通过质谱分析,我们确定了 YTHDF1 对心肌细胞膜筏蛋白表达的必要性。具体来说,YTHDF1 与 m6A 修饰的 Caveolin 1(Cav1)mRNA 结合,并促进其翻译。我们进一步证实,YTHDF1 可调控下游 ERK 信号转导。总之,我们的研究结果凸显了 YTHDF1 作为腔壁蛋白转录后调节因子的新作用,它是维持心脏功能所必需的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

YTHDF1 is pivotal for maintenance of cardiac homeostasis

YTHDF1 is pivotal for maintenance of cardiac homeostasis

The YTH-domain family (YTHDF) of RNA binding proteins can control gene expression at the post-transcriptional level by regulating mRNAs with N6-methyladenosine (m6A) modifications. Despite the established importance of m6A in the heart, the cardiac role of specific m6A-binding proteins remains unclear. Here, we characterized the function of YTHDF1 in cardiomyocytes using a newly generated cardiac-restricted mouse model. Deletion of YTHDF1 in adult cardiomyocytes led to hypertrophy, fibrosis, and dysfunction. Using mass spectrometry, we identified the necessity of YTHDF1 for the expression of cardiomyocyte membrane raft proteins. Specifically, YTHDF1 bound to m6A-modified Caveolin 1 (Cav1) mRNA and favored its translation. We further demonstrated that YTHDF1 regulates downstream ERK signaling. Altogether, our findings highlight a novel role for YTHDF1 as a post-transcriptional regulator of caveolar proteins which is necessary for the maintenance of cardiac function.

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来源期刊
CiteScore
10.70
自引率
0.00%
发文量
171
审稿时长
42 days
期刊介绍: The Journal of Molecular and Cellular Cardiology publishes work advancing knowledge of the mechanisms responsible for both normal and diseased cardiovascular function. To this end papers are published in all relevant areas. These include (but are not limited to): structural biology; genetics; proteomics; morphology; stem cells; molecular biology; metabolism; biophysics; bioengineering; computational modeling and systems analysis; electrophysiology; pharmacology and physiology. Papers are encouraged with both basic and translational approaches. The journal is directed not only to basic scientists but also to clinical cardiologists who wish to follow the rapidly advancing frontiers of basic knowledge of the heart and circulation.
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