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原生质体膨胀和下胚轴生长依赖于不同的生长素信号通路。

Protoplast Swelling and Hypocotyl Growth Depend on Different Auxin Signaling Pathways.

机构信息

Plant Physiology, Faculty of Biology, University of Marburg, 35043 Marburg, Germany.

Molecular Plant Physiology, Department of Biology, University of Hamburg, 22609 Hamburg, Germany.

出版信息

Plant Physiol. 2017 Oct;175(2):982-994. doi: 10.1104/pp.17.00733. Epub 2017 Aug 31.

Abstract

Members of the TRANSPORT INHIBITOR RESPONSE1/AUXIN SIGNALING F-BOX PROTEIN (TIR1/AFB) family are known auxin receptors. To analyze the possible receptor function of AUXIN BINDING PROTEIN1 (ABP1), an auxin receptor currently under debate, we performed different approaches. We performed a pharmacological approach using α-(2,4-dimethylphenylethyl-2-oxo)-indole-3-acetic acid (auxinole), α-(phenylethyl-2-oxo)-indole-3-acetic acid (PEO-IAA), and 5-fluoroindole-3-acetic acid (5-F-IAA) to discriminate between ABP1- and TIR1/AFB-mediated processes in Arabidopsis (). We used a peptide of the carboxyl-terminal region of AtABP1 as a tool. We performed mutant analysis with the null alleles of , and , and the TILLING mutant We employed Coimbra, an accession that exhibits an amino acid exchange in the auxin-binding domain of ABP1. We measured either volume changes of single hypocotyl protoplasts or hypocotyl growth, both at high temporal resolution. 5-F-IAA selectively activated the TIR1/AFB pathway but did not induce protoplast swelling; instead, it showed auxin activity in the hypocotyl growth test. In contrast, PEO-IAA induced an auxin-like swelling response but no hypocotyl growth. The carboxyl-terminal peptide of AtABP1 induced an auxin-like swelling response. In the -related mutants and Coimbra, no auxin-induced protoplast swelling occurred. ABP1 seems to be involved in mediating rapid auxin-induced protoplast swelling, but it is not involved in the control of rapid auxin-induced growth.

摘要

TRANSPORT INHIBITOR RESPONSE1/AUXIN SIGNALING F-BOX PROTEIN(TIR1/AFB)家族的成员是已知的生长素受体。为了分析目前备受争议的生长素受体 AUXIN BINDING PROTEIN1(ABP1)的可能受体功能,我们采用了不同的方法。我们使用了药理学方法,使用了α-(2,4-二甲基苯乙基-2-氧代)-吲哚-3-乙酸(生长素)、α-(苯乙基-2-氧代)-吲哚-3-乙酸(PEO-IAA)和 5-氟吲哚-3-乙酸(5-F-IAA),以区分拟南芥中 ABP1-和 TIR1/AFB 介导的过程()。我们使用了 AtABP1 羧基末端区域的肽作为工具。我们使用了 null 等位基因、和、以及 TILLING 突变体的突变分析。我们使用了 Coimbra 品系,该品系在 ABP1 的生长素结合域中表现出氨基酸交换。我们测量了单个下胚轴原生质体的体积变化或下胚轴生长,两者都具有高时间分辨率。5-F-IAA 选择性激活 TIR1/AFB 途径,但不会诱导原生质体膨胀;相反,它在下胚轴生长试验中表现出生长素活性。相比之下,PEO-IAA 诱导出类似生长素的膨胀反应,但不会引起下胚轴生长。AtABP1 的羧基末端肽诱导出类似生长素的膨胀反应。在相关的突变体和 Coimbra 中,没有发生生长素诱导的原生质体膨胀。ABP1 似乎参与介导快速生长素诱导的原生质体膨胀,但不参与快速生长素诱导生长的控制。

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