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Ankrd6是果蝇平面细胞极性基因diego的哺乳动物功能同源物,并调节小鼠内耳中细胞的协调定向。

Ankrd6 is a mammalian functional homolog of Drosophila planar cell polarity gene diego and regulates coordinated cellular orientation in the mouse inner ear.

作者信息

Jones Chonnettia, Qian Dong, Kim Sun Myoung, Li Shuangding, Ren Dongdong, Knapp Lindsey, Sprinzak David, Avraham Karen B, Matsuzaki Fumio, Chi Fanglu, Chen Ping

机构信息

Department of Cell Biology, Emory University, Atlanta, GA 30322, USA.

Department of Cell Biology, Emory University, Atlanta, GA 30322, USA.

出版信息

Dev Biol. 2014 Nov 1;395(1):62-72. doi: 10.1016/j.ydbio.2014.08.029. Epub 2014 Sep 10.

DOI:10.1016/j.ydbio.2014.08.029
PMID:25218921
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4837453/
Abstract

The coordinated polarization of neighboring cells within the plane of the tissue, known as planar cell polarity (PCP), is a recurring theme in biology. It is required for numerous developmental processes for the form and function of many tissues and organs across species. The genetic pathway regulating PCP was first discovered in Drosophila, and an analogous but distinct pathway is emerging in vertebrates. It consists of membrane protein complexes known as core PCP proteins that are conserved across species. Here we report that the over-expression of the murine Ankrd6 (mAnkrd6) gene that shares homology with Drosophila core PCP gene diego causes a typical PCP phenotype in Drosophila, and mAnkrd6 can rescue the loss of function of diego in Drosophila. In mice, mAnkrd6 protein is asymmetrically localized in cells of the inner ear sensory organs, characteristic of components of conserved core PCP complexes. The loss of mAnkrd6 causes PCP defects in the inner ear sensory organs. Moreover, canonical Wnt signaling is significantly increased in mouse embryonic fibroblasts from mAnkrd6 knockout mice in comparison to wild type controls. Together, these results indicated that mAnkrd6 is a functional homolog of the Drosophila diego gene for mammalian PCP regulation and act to suppress canonical Wnt signaling.

摘要

组织平面内相邻细胞的协同极化,即平面细胞极性(PCP),是生物学中反复出现的一个主题。它是许多物种中众多组织和器官的形态与功能发育过程所必需的。调节PCP的遗传途径最初是在果蝇中发现的,而在脊椎动物中也出现了一条类似但不同的途径。它由被称为核心PCP蛋白的膜蛋白复合物组成,这些复合物在物种间是保守的。在此,我们报告称,与果蝇核心PCP基因diego具有同源性的小鼠Ankrd6(mAnkrd6)基因的过表达会在果蝇中导致典型的PCP表型,并且mAnkrd6可以挽救果蝇中diego的功能丧失。在小鼠中,mAnkrd6蛋白不对称地定位于内耳感觉器官的细胞中,这是保守的核心PCP复合物成分的特征。mAnkrd6的缺失会导致内耳感觉器官出现PCP缺陷。此外,与野生型对照相比,来自mAnkrd6基因敲除小鼠的小鼠胚胎成纤维细胞中经典Wnt信号显著增加。这些结果共同表明,mAnkrd6是果蝇diego基因在哺乳动物PCP调节中的功能同源物,并起到抑制经典Wnt信号的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/fd3731bf488b/nihms627189f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/16aaacf44179/nihms627189f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/ea48314e5de0/nihms627189f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/a0f5854bd511/nihms627189f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/c439988b3011/nihms627189f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/f437e4d3c4ac/nihms627189f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/fd3731bf488b/nihms627189f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/16aaacf44179/nihms627189f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/ea48314e5de0/nihms627189f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/a0f5854bd511/nihms627189f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/c439988b3011/nihms627189f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/f437e4d3c4ac/nihms627189f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3747/4837453/fd3731bf488b/nihms627189f6.jpg

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