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通过调节生长素转运体稳态,Arp2/3复合物是生长素驱动细胞扩张所必需的。

Arp2/3 Complex Is Required for Auxin-Driven Cell Expansion Through Regulation of Auxin Transporter Homeostasis.

作者信息

García-González Judith, Kebrlová Štépánka, Semerák Matěj, Lacek Jozef, Kotannal Baby Innu, Petrášek Jan, Schwarzerová Kateřina

机构信息

Department of Experimental Plant Biology, Faculty of Science, Charles University, Prague, Czechia.

Institute of Experimental Botany, Czech Academy of Sciences, Prague, Czechia.

出版信息

Front Plant Sci. 2020 Apr 28;11:486. doi: 10.3389/fpls.2020.00486. eCollection 2020.

DOI:10.3389/fpls.2020.00486
PMID:32425966
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7212389/
Abstract

The Arp2/3 complex is an actin nucleator shown to be required throughout plant morphogenesis, contributing to processes such as cell expansion, tissue differentiation or cell wall assembly. A recent publication demonstrated that plants lacking functional Arp2/3 complex also present defects in auxin distribution and transport. This work shows that Arp2/3 complex subunits are predominantly expressed in the provasculature, although other plant tissues also show promoter activity (e.g., cotyledons, apical meristems, or root tip). Moreover, auxin can trigger subunit expression, indicating a role of this phytohormone in mediating the complex activity. Further investigation of the functional interaction between Arp2/3 complex and auxin signaling also reveals their cooperation in determining pavement cell shape, presumably through the role of Arp2/3 complex in the correct auxin carrier trafficking. Young seedlings of mutants show increased auxin-triggered proteasomal degradation of DII-VENUS and altered PIN3 distribution, with higher levels of the protein in the vacuole. Closer observation of vacuolar morphology revealed the presence of a more fragmented vacuolar compartment when Arp2/3 function is abolished, hinting a generalized role of Arp2/3 complex in endomembrane function and protein trafficking.

摘要

Arp2/3复合体是一种肌动蛋白成核因子,已证实在整个植物形态发生过程中都是必需的,参与细胞扩张、组织分化或细胞壁组装等过程。最近的一篇出版物表明,缺乏功能性Arp2/3复合体的植物在生长素分布和运输方面也存在缺陷。这项研究表明,Arp2/3复合体亚基主要在原维管系统中表达,尽管其他植物组织也显示出启动子活性(如子叶、顶端分生组织或根尖)。此外,生长素可以触发亚基表达,表明这种植物激素在介导复合体活性中发挥作用。对Arp2/3复合体与生长素信号传导之间功能相互作用的进一步研究还揭示了它们在确定扁平细胞形状方面的协同作用,推测是通过Arp2/3复合体在正确的生长素载体运输中的作用。突变体的幼苗显示出生长素触发的DII-VENUS蛋白酶体降解增加以及PIN3分布改变,液泡中该蛋白水平更高。对液泡形态的更仔细观察发现,当Arp2/3功能被消除时,存在更碎片化的液泡区室,这暗示了Arp2/3复合体在内膜功能和蛋白质运输中的普遍作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/e4add011d4cf/fpls-11-00486-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/4f5381c5e62f/fpls-11-00486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/7cb254577f2f/fpls-11-00486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/04e124bb5663/fpls-11-00486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/392a890ce22e/fpls-11-00486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/f791683902de/fpls-11-00486-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/755451898cc4/fpls-11-00486-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/1686e54e433e/fpls-11-00486-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/efee70b0e2f2/fpls-11-00486-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/e4add011d4cf/fpls-11-00486-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/4f5381c5e62f/fpls-11-00486-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/7cb254577f2f/fpls-11-00486-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/04e124bb5663/fpls-11-00486-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/392a890ce22e/fpls-11-00486-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/f791683902de/fpls-11-00486-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/755451898cc4/fpls-11-00486-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/1686e54e433e/fpls-11-00486-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/efee70b0e2f2/fpls-11-00486-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5c86/7212389/e4add011d4cf/fpls-11-00486-g009.jpg

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