4.7 Article

Complexity of the auxin biosynthetic network in Arabidopsis hypocotyls is revealed by multiple stable-labeled precursors

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PHYTOCHEMISTRY
卷 200, 期 -, 页码 -

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.phytochem.2022.113219

关键词

Arabidopsis thaliana; Brassicaceae; Mouse ear cress; Targeted metabolomics; Indole; Auxin; IAA biosynthesis; Phytohormones; Stable isotopes; Tryptophan

资金

  1. Agriculture and Food Research Initiative competitive awards [2018-67011-28056, 2018-67013-27503, 2019-51181-30025]
  2. USDA National Institute of Food and Agriculture, NSF Plant Genome Research Program [IOS-1238812]
  3. Minnesota Agricultural Experiment Station

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This study investigated the contributions of different biosynthetic pathways to auxin synthesis in Arabidopsis plants. It found that auxin synthesis dependent on tryptophan through the IPyA pathway plays a major role in de-etiolating hypocotyls and can be effectively blocked using chemical inhibitors. The labeling treatment results showed that auxin synthesized from indole through [C-13(6)]anthranilate was more abundant than from [N-15(1)]indole.
Auxin is a key regulator of plant development and in Arabidopsis thaliana can be synthesized through multiple pathways; however, the contributions of various biosynthetic pathways to specific developmental processes are largely unknown. To trace the involvement of various biosynthetic routes to indole-3-acetic acid (IAA) under conditions that induce adventitious root formation in Arabidopsis hypocotyls, we treated seedlings with three different stable isotope-labeled precursors ([C-13(6)]anthranilate, [N-15(1)]indole, and [C-13(3)]serine) and monitored label incorporation into a number of proposed biosynthesis intermediates as well as IAA. We also employed inhibitors targeting tryptophan aminotransferases and flavin monooxygenases of the IPyA pathway, and treatment with these inhibitors differentially altered the labeling patterns from all three precursors into intermediate compounds and IAA. [C-13(3)]Serine was used to trace utilization of tryptophan (Trp) and downstream intermediates by monitoring C-13 incorporation into Trp, indole-3-pyruvic acid (IPyA), and IAA; most C-13 incorporation into IAA was eliminated with inhibitor treatments, suggesting Trp-dependent IAA biosynthesis through the IPyA pathway is a dominant contributor to the auxin pool in de-etiolating hypocotyls that can be effectively blocked using chemical inhibitors. Labeling treatment with both [C-13(6)]anthranilate and [N-15(1)]indole simultaneously resulted in higher label incorporation into IAA through [N-15(1)]indole than through [C-13(6)]anthranilate; however, this trend was reversed in the proposed precursors that were monitored, with the majority of isotope label originating from [C-13(6)]anthranilate. An even greater proportion of IAA became [N-15(1)]-labeled compared to [C-13(6)]-labeled in seedlings treated with IPyA pathway inhibitors, suggesting that, when the IPyA pathway is blocked, IAA biosynthesis from labeled indole may also come from an origin independent of the measured pool of Trp in these tissues.

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