The Intracellular Loop 2 F328S Frizzled-4 Mutation Implicated in Familial Exudative Vitreoretinopathy Impairs Dishevelled Recruitment.

Q2 Biochemistry, Genetics and Molecular Biology Journal of Molecular Signaling Pub Date : 2015-11-24 DOI:10.5334/1750-2187-10-6
Milly S Pau, Shujuan Gao, Craig C Malbon, Hsien-Yu Wang, Alexander C Bertalovitz
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引用次数: 9

Abstract

Familial exudative vitreoretinopathy (FEVR) is a disease state characterized by aberrant retinal angiogenesis. Norrin-induced activation of Frizzled-4 (Fz4) has a major role in regulating beta-catenin levels in the eye that, in turn, modulate the blood retina barrier (BRB). Here we gain insight on the basis of the pathology of a FEVR implicated F328S Fz4 mutant by study. The receptor exhibits a substantially reduced ability to activate Lef/Tcf-dependent transcription. This impaired activation correlates with a decreased ability to stabilize and recruit Dishevelled-2 (Dvl2) to the cell surface. Aromaticity at position 328 of the intracellular loop 2 (iloop2) is revealed similarly as a prerequisite for Dvl2 recruitment to the Fz4. This aromaticity at 328 enables normal Norrin-induced canonical activation. The corresponding position in iloop2 of other Frizzleds likely functions in Dvl recruitment.

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与家族性渗出性玻璃体视网膜病变有关的细胞内环2 F328S卷曲-4突变损害了散乱募集。
家族性渗出性玻璃体视网膜病变(FEVR)是一种以异常视网膜血管生成为特征的疾病状态。norrin诱导的frizzled4 (Fz4)的激活在调节眼睛中的β -连环蛋白水平中起主要作用,进而调节血液视网膜屏障(BRB)。本文通过对F328S Fz4突变株FEVR的病理研究,深入了解了F328S Fz4突变株FEVR的病理特征。受体表现出显著降低的激活左/ tcf依赖性转录的能力。这种受损的激活与稳定和招募disheveled -2 (Dvl2)到细胞表面的能力下降有关。细胞内环2 (iloop2) 328位的芳香性同样被揭示为Dvl2募集到Fz4的先决条件。328的芳香性使正常的norrin诱导的规范激活成为可能。其他Frizzleds的iloop2中相应的位置可能在Dvl招募中起作用。
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Journal of Molecular Signaling
Journal of Molecular Signaling Biochemistry, Genetics and Molecular Biology-Biochemistry
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期刊介绍: Journal of Molecular Signaling is an open access, peer-reviewed online journal that encompasses all aspects of molecular signaling. Molecular signaling is an exponentially growing field that encompasses different molecular aspects of cell signaling underlying normal and pathological conditions. Specifically, the research area of the journal is on the normal or aberrant molecular mechanisms involving receptors, G-proteins, kinases, phosphatases, and transcription factors in regulating cell proliferation, differentiation, apoptosis, and oncogenesis in mammalian cells. This area also covers the genetic and epigenetic changes that modulate the signaling properties of cells and the resultant physiological conditions.
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