Hisaoka Shiho, Osawa Jin, Kobashi Riku, Ishida Atsuhiko, Kameshita Isamu, Sueyoshi Noriyuki
Department of Life Sciences, Faculty of Agriculture, Kagawa University, Kagawa, 761-0795, Japan.
Laboratory of Molecular Brain Science, Graduate School of Integrated Arts and Sciences, Hiroshima University, Higashi-Hiroshima, 739-8521, Japan.
Biochem Biophys Res Commun. 2023 Mar 15;649:16-24. doi: 10.1016/j.bbrc.2023.01.076. Epub 2023 Jan 25.
Bone morphogenetic protein 2 (BMP2)-inducible kinase (BMP2K) is induced by the cytokine BMP2, which is also implicated in the production of bone differentiation. In addition to regulating bone differentiation, BMP2K is implicated in a variety of cancers. Therefore, understanding the variables that determine where in the cell this kinase functions may help in understanding malignancies linked to BMP2K. However, the mechanisms regulating the subcellular localization of BMP2K are mainly unknown. By liquid-liquid phase separation (LLPS), BMP2K forms droplets in the cytoplasm, but how the droplets are regulated remains unclear. The reason why BMP2K localizes to the cytoplasm irrespective of having a nuclear localization signal (NLS) is also unknown. Here we show the element that controls BMP2K's LLPS and cytoplasmic localization. A glutamine-rich area is necessary for BMP2K phase separation, and droplet formation is controlled by hyperosmolarity. Cytoplasmic localization of BMP2K is managed by inhibition of NLS function through phosphorylation of Ser-1010 and by a newly found cytoplasmic localization region that antagonizes the NLS. These results will provide an important biochemical foundation for the advancement of BMP2K-related cell biology, structural biology, and pathophysiology.
骨形态发生蛋白2(BMP2)诱导激酶(BMP2K)由细胞因子BMP2诱导产生,BMP2也与骨分化的产生有关。除了调节骨分化外,BMP2K还与多种癌症有关。因此,了解决定该激酶在细胞中功能位置的变量可能有助于理解与BMP2K相关的恶性肿瘤。然而,调节BMP2K亚细胞定位的机制主要尚不清楚。通过液-液相分离(LLPS),BMP2K在细胞质中形成液滴,但液滴如何被调节仍不清楚。BMP2K无论有无核定位信号(NLS)都定位于细胞质的原因也不清楚。在这里,我们展示了控制BMP2K的LLPS和细胞质定位的元件。富含谷氨酰胺的区域是BMP2K相分离所必需的,液滴形成受高渗调节。BMP2K的细胞质定位是通过Ser-1010的磷酸化抑制NLS功能以及一个新发现的与NLS拮抗的细胞质定位区域来实现的。这些结果将为推进与BMP2K相关的细胞生物学、结构生物学和病理生理学提供重要的生化基础。