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锚蛋白相关蛋白复合体(APC)是皮质微管网络组织模板的一个组成部分。

APC is a component of an organizing template for cortical microtubule networks.

作者信息

Reilein Amy, Nelson W James

机构信息

Department of Molecular and Cellular Physiology, Beckman Center for Molecular and Genetic Medicine B121, 279 Campus Drive, Stanford University School of Medicine, Stanford, CA 94305-5435, USA.

出版信息

Nat Cell Biol. 2005 May;7(5):463-73. doi: 10.1038/ncb1248.

DOI:10.1038/ncb1248
PMID:15892196
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3368611/
Abstract

A microtubule network on the basal cortex of polarized epithelial cells consists of non-centrosomal microtubules of mixed polarity. Here, we investigate the proteins that are involved in organizing this network, and we show that end-binding protein 1 (EB1), adenomatous polyposis coli protein (APC) and p150Glued - although considered to be microtubule plus-end-binding proteins - are localized along the entire length of microtubules within the network, and at T-junctions between microtubules. The network shows microtubule behaviours that arise from physical interactions between microtubules, including microtubule plus-end stabilization on the sides of other microtubules, and sliding of microtubule ends along other microtubules. APC also localizes to the basal cortex. Microtubules grew over and paused at APC puncta; an in vitro reconstituted microtubule network overlaid APC puncta; and microtubule network reconstitution was inhibited by function-blocking APC antibodies. Thus, APC is a component of a cortical template that guides microtubule network formation.

摘要

极化上皮细胞基底皮质上的微管网络由混合极性的非中心体微管组成。在此,我们研究参与组织该网络的蛋白质,并表明端结合蛋白1(EB1)、腺瘤性息肉病大肠杆菌蛋白(APC)和p150Glued——尽管被认为是微管正端结合蛋白——定位于网络内微管的整个长度以及微管之间的T形接头处。该网络显示出由微管之间的物理相互作用产生的微管行为,包括其他微管侧面的微管正端稳定以及微管末端沿其他微管的滑动。APC也定位于基底皮质。微管在APC点上生长并暂停;体外重建的微管网络覆盖了APC点;功能阻断性APC抗体抑制了微管网络的重建。因此,APC是指导微管网络形成的皮质模板的一个组成部分。

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APC is a component of an organizing template for cortical microtubule networks.锚蛋白相关蛋白复合体(APC)是皮质微管网络组织模板的一个组成部分。
Nat Cell Biol. 2005 May;7(5):463-73. doi: 10.1038/ncb1248.
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本文引用的文献

1
CLASP1 and CLASP2 bind to EB1 and regulate microtubule plus-end dynamics at the cell cortex.CLASP1和CLASP2与EB1结合,并在细胞皮层调节微管正端动力学。
J Cell Biol. 2005 Jan 3;168(1):141-53. doi: 10.1083/jcb.200405094.
2
Cell-adhesion assays: fabrication of an E-cadherin substratum and isolation of lateral and Basal membrane patches.细胞黏附测定:E-钙黏蛋白基质的制备以及侧向和基底膜片的分离。
Methods Mol Biol. 2005;294:303-20. doi: 10.1385/1-59259-860-9:303.
3
Interaction with IQGAP1 links APC to Rac1, Cdc42, and actin filaments during cell polarization and migration.在细胞极化和迁移过程中,与IQGAP1的相互作用将腺瘤性息肉病蛋白(APC)与Rac1、Cdc42和肌动蛋白丝联系起来。
Dev Cell. 2004 Dec;7(6):871-83. doi: 10.1016/j.devcel.2004.10.017.
4
Surfing, regulating and capturing: are all microtubule-tip-tracking proteins created equal?冲浪、调控与捕获:所有微管尖端追踪蛋白都一样吗?
Trends Cell Biol. 2004 Sep;14(9):491-6. doi: 10.1016/j.tcb.2004.07.011.
5
EB1 and APC bind to mDia to stabilize microtubules downstream of Rho and promote cell migration.EB1和APC与mDia结合,以稳定Rho下游的微管并促进细胞迁移。
Nat Cell Biol. 2004 Sep;6(9):820-30. doi: 10.1038/ncb1160. Epub 2004 Aug 15.
6
NGF-induced axon growth is mediated by localized inactivation of GSK-3beta and functions of the microtubule plus end binding protein APC.神经生长因子诱导的轴突生长由糖原合成酶激酶3β的局部失活和微管正端结合蛋白APC的功能介导。
Neuron. 2004 Jun 24;42(6):897-912. doi: 10.1016/j.neuron.2004.05.011.
7
Cortical control of microtubule stability and polarization.皮层对微管稳定性和极化的控制。
Curr Opin Cell Biol. 2004 Feb;16(1):106-12. doi: 10.1016/j.ceb.2003.11.010.
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"Search-and-capture" of microtubules through plus-end-binding proteins (+TIPs).通过正端结合蛋白(+TIPs)对微管进行“搜索与捕获”
J Biochem. 2003 Sep;134(3):321-6. doi: 10.1093/jb/mvg148.
9
Orientation of asymmetric stem cell division by the APC tumor suppressor and centrosome.APC肿瘤抑制因子和中心体对不对称干细胞分裂的定向作用
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Nanometer targeting of microtubules to focal adhesions.微管向黏着斑的纳米靶向作用。
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