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Fyn介导的Menin磷酸化破坏干细胞中的端粒维持。

Fyn-mediated phosphorylation of Menin disrupts telomere maintenance in stem cells.

作者信息

Paul Souren, McCourt Preston M, Le Le Thi My, Ryu Joohyun, Czaja Wioletta, Bode Ann M, Contreras-Galindo Rafael, Dong Zigang

机构信息

The Hormel Institute, University of Minnesota, 801 16th Avenue NE, Austin, MN 55912, USA.

Department of Laboratory Medicine and Pathology, University of Minnesota School of Medicine, Minneapolis, MN, USA.

出版信息

bioRxiv. 2024 Mar 19:2023.10.04.560876. doi: 10.1101/2023.10.04.560876.

Abstract

Telomeres protect chromosome ends and determine the replication potential of dividing cells. The canonical telomere sequence TTAGGG is synthesized by telomerase holoenzyme, which maintains telomere length in proliferative stem cells. Although the core components of telomerase are well-defined, mechanisms of telomerase regulation are still under investigation. We report a novel role for the Src family kinase Fyn, which disrupts telomere maintenance in stem cells by phosphorylating the scaffold protein Menin. We found that Fyn knockdown prevented telomere erosion in human and mouse stem cells, validating the results with four telomere measurement techniques. We show that Fyn phosphorylates Menin at tyrosine 603 (Y603), which increases Menin's SUMO1 modification, C-terminal stability, and importantly, its association with the telomerase RNA component (TR). Using mass spectrometry, immunoprecipitation, and immunofluorescence experiments we found that SUMO1-Menin decreases TR's association with telomerase subunit Dyskerin, suggesting that Fyn's phosphorylation of Menin induces telomerase subunit mislocalization and may compromise telomerase function at telomeres. Importantly, we find that Fyn inhibition reduces accelerated telomere shortening in human iPSCs harboring mutations for dyskeratosis congenita.

摘要

端粒保护染色体末端并决定分裂细胞的复制潜能。典型的端粒序列TTAGGG由端粒酶全酶合成,端粒酶全酶在增殖性干细胞中维持端粒长度。尽管端粒酶的核心成分已明确,但端粒酶的调控机制仍在研究中。我们报道了Src家族激酶Fyn的一种新作用,它通过磷酸化支架蛋白Menin破坏干细胞中的端粒维持。我们发现敲低Fyn可防止人类和小鼠干细胞中的端粒侵蚀,并用四种端粒测量技术验证了结果。我们表明Fyn在酪氨酸603(Y603)处磷酸化Menin,这增加了Menin的SUMO1修饰、C末端稳定性,重要的是,增加了其与端粒酶RNA成分(TR)的结合。通过质谱、免疫沉淀和免疫荧光实验,我们发现SUMO1-Menin降低了TR与端粒酶亚基戴斯科特林的结合,这表明Fyn对Menin的磷酸化诱导了端粒酶亚基的错误定位,并可能损害端粒处的端粒酶功能。重要的是,我们发现抑制Fyn可减少携带先天性角化不良突变的人类诱导多能干细胞中端粒的加速缩短。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a67f/10958554/08e8233ee06e/nihpp-2023.10.04.560876v2-f0001.jpg

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