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Mst4和埃兹蛋白在Lkb1/Strad/Mo25极化复合体下游诱导刷状缘的形成。

Mst4 and Ezrin induce brush borders downstream of the Lkb1/Strad/Mo25 polarization complex.

作者信息

ten Klooster Jean Paul, Jansen Marnix, Yuan Jin, Oorschot Viola, Begthel Harry, Di Giacomo Valeria, Colland Frédéric, de Koning John, Maurice Madelon M, Hornbeck Peter, Clevers Hans

机构信息

Hubrecht Institute, KNAW and University Medical Centre, Utrecht, The Netherlands.

出版信息

Dev Cell. 2009 Apr;16(4):551-62. doi: 10.1016/j.devcel.2009.01.016.

Abstract

The human Lkb1 kinase, encoded by the ortholog of the invertebrate Par4 polarity gene, is mutated in Peutz-Jeghers cancer syndrome. Lkb1 activity requires complex formation with the pseudokinase Strad and the adaptor protein Mo25. The complex can induce complete polarization in a single isolated intestinal epithelial cell. We describe an interaction between Mo25alpha and a human serine/threonine kinase termed Mst4. A homologous interaction occurs in the yeast Schizosaccharomyces pombe in the control of polar tip growth. Human Mst4 translocates from the Golgi to the subapical membrane compartment upon activation of Lkb1. Inhibition of Mst4 activity inhibits Lkb1-induced brush border formation, whereas other aspects of polarity such as the formation of lateral junctions remain unaffected. As an essential event in brush border formation, Mst4 phosphorylates the regulatory T567 residue of Ezrin. These data define a brush border induction pathway downstream of the Lkb1/Strad/Mo25 polarization complex, yet separate from other polarity events.

摘要

人类Lkb1激酶由无脊椎动物Par4极性基因的直系同源基因编码,在黑斑息肉综合征中发生突变。Lkb1的活性需要与假激酶Strad和衔接蛋白Mo25形成复合物。该复合物可在单个分离的肠上皮细胞中诱导完全极化。我们描述了Mo25α与一种名为Mst4的人类丝氨酸/苏氨酸激酶之间的相互作用。在酵母粟酒裂殖酵母中,一种同源相互作用发生在极性尖端生长的控制过程中。Lkb1激活后,人类Mst4从高尔基体转移至顶端下膜区室。抑制Mst4活性会抑制Lkb1诱导的刷状缘形成,而极性的其他方面,如侧连接的形成则不受影响。作为刷状缘形成中的一个关键事件,Mst4使埃兹蛋白的调节性T567残基磷酸化。这些数据定义了一条位于Lkb1/Strad/Mo25极化复合物下游、但与其他极性事件不同的刷状缘诱导途径。

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