Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/118078
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Type: Journal article
Title: Lateral branching oxidoreductase acts in the final stages of strigolactone biosynthesis in Arabidopsis
Author: Brewer, P.
Yoneyama, K.
Filardo, F.
Meyers, E.
Scaffidi, A.
Frickey, T.
Akiyama, K.
Seto, Y.
Dun, E.
Cremer, J.
Kerr, S.
Waters, M.
Flematti, G.
Mason, M.
Weiller, G.
Yamaguchi, S.
Nomura, T.
Smith, S.
Yoneyama, K.
Beveridge, C.
Citation: Proceedings of the National Academy of Sciences of the United States of America, 2016; 113(22):6301-6306
Publisher: National Academy of Sciences
Issue Date: 2016
ISSN: 0027-8424
1091-6490
Statement of
Responsibility: 
Philip B. Brewer, Kaori Yoneyama, Fiona Filardo, Emma Meyers, Adrian Scaffidid, Tancred Frickey ... et al.
Abstract: Strigolactones are a group of plant compounds of diverse but related chemical structures. They have similar bioactivity across a broad range of plant species, act to optimize plant growth and development, and promote soil microbe interactions. Carlactone, a common precursor to strigolactones, is produced by conserved enzymes found in a number of diverse species. Versions of the MORE AXILLARY GROWTH1 (MAX1) cytochrome P450 from rice and Arabidopsis thaliana make specific subsets of strigolactones from carlactone. However, the diversity of natural strigolactones suggests that additional enzymes are involved and remain to be discovered. Here, we use an innovative method that has revealed a missing enzyme involved in strigolactone metabolism. By using a transcriptomics approach involving a range of treatments that modify strigolactone biosynthesis gene expression coupled with reverse genetics, we identified LATERAL BRANCHING OXIDOREDUCTASE (LBO), a gene encoding an oxidoreductase-like enzyme of the 2-oxoglutarate and Fe(II)-dependent dioxygenase superfamily. Arabidopsis lbo mutants exhibited increased shoot branching, but the lbo mutation did not enhance the max mutant phenotype. Grafting indicated that LBO is required for a graft-transmissible signal that, in turn, requires a product of MAX1. Mutant lbo backgrounds showed reduced responses to carlactone, the substrate of MAX1, and methyl carlactonoate (MeCLA), a product downstream of MAX1. Furthermore, lbo mutants contained increased amounts of these compounds, and the LBO protein specifically converts MeCLA to an unidentified strigolactone-like compound. Thus, LBO function may be important in the later steps of strigolactone biosynthesis to inhibit shoot branching in Arabidopsis and other seed plants.
Keywords: Plant; branching; strigolactone; biosynthesis; Arabidopsis
Rights: The author(s) retains copyright to individual PNAS articles, and the National Academy of Sciences of the United States of America (NAS) holds copyright to the collective work and retains an exclusive License to Publish these articles, except for open access articles submitted beginning September 2017. For such open access articles, NAS retains a nonexclusive License to Publish, and these articles are distributed under either a CC BY-NC-ND or CC BY license. For volumes 106–114 (2009–September 2017), the author(s) retains copyright to individual articles, and NAS retains an exclusive License to Publish these articles and holds copyright to the collective work.
RMID: 0030107611
DOI: 10.1073/pnas.1601729113
Grant ID: http://purl.org/au-research/grants/arc/DP110100997
http://purl.org/au-research/grants/arc/DP130103646
Appears in Collections:Agriculture, Food and Wine publications

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