Plant Physiology, Faculty of Biology, University of Marburg, 35043 Marburg, Germany.
Molecular Plant Physiology, Department of Biology, University of Hamburg, 22609 Hamburg, Germany.
Plant Physiol. 2017 Oct;175(2):982-994. doi: 10.1104/pp.17.00733. Epub 2017 Aug 31.
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.
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。