Does zaxinone counteract strigolactones in shaping rice architecture?

References

• Al-Babili S, Bouwmeester HJ. Strigolactones, a novel carotenoid-derived plant hormone. Annu Rev Plant Biol. 2015;66:161–4. doi:10.1146/annurev-arplant-043014-114759.
   PubMed Web of Science ®Google Scholar
• Wang JY, Lin P-Y, Al-Babili S, et al. (2021a). On the biosynthesis and evolution of apocarotenoid plant growth regulators. Seminars in Cell and Developmental Biolology 109, 3–11. doi: 10.1016/j.semcdb.2020.07.007
   Google Scholar
• Yoneyama K, Xie X, Yoneyama K, Kisugi T, Nomura T, Nakatani Y, Akiyama K, McErlean CSP. Which Are the Major Players, Canonical or Non-Canonical Strigolactones? J Exp Bot. 2018;69(9):2231–2239. https://doi.org/10.1093/jxb/ery090.
   PubMed Web of Science ®Google Scholar
• Alder A, Jamil M, Marzorati M, Bruno M, Vermathen M, Bigler P, Ghisla S, Bouwmeester H, Beyer P, Al-Babili S, et al. The path from β-carotene to carlactone, a strigolactone-like plant hormone. Science. 2012;335(6074):1348–1351. doi:10.1126/science.1218094.
   PubMed Web of Science ®Google Scholar
• Abuauf H, Haider I, Jia K-P, Ablazov A, Mi J, Blilou I, Al-Babili S. The arabidopsis DWARF27 gene encodes an all-trans-/9-cis-β-carotene isomerase and is induced by auxin, abscisic acid and phosphate deficiency. Plant Science. 2018;277:33–42. doi:10.1016/j.plantsci.2018.06.024.
   PubMed Web of Science ®Google Scholar
• Bruno M, et al. On the substrate-and stereospecificity of the plant carotenoid cleavage dioxygenase 7. FEBS Lett. 2014;588:1802–1807. doi:10.1016/j.febslet.2014.03.041.
   PubMed Web of Science ®Google Scholar
• Bruno M, et al. Insights into the formation of carlactone from in-depth analysis of the CCD 8-catalyzed reactions. FEBS Lett. 2017;591:792–800. doi:10.1002/1873-3468.12593.
   PubMed Web of Science ®Google Scholar
• Chen G-TE, et al. 9‑cis‑β‑Apo‑10ʹ‑carotenal is the precursor of strigolactones in planta. Planta. 2022;256:88. doi:10.1007/s00425-022-03999-9.
   Web of Science ®Google Scholar
• Zhang Y, van Dijk ADJ, Scaffidi A, Flematti GR, Hofmann M, Charnikhova T, Verstappen F, Hepworth J, van der Krol S, Leyser O, et al. Rice cytochrome P450 MAX1 homologs catalyze distinct steps in strigolactone biosynthesis. Nat Chem Biol. 2014;10(12):1028–1033. doi:10.1038/nchembio.1660.
   PubMed Web of Science ®Google Scholar
• Umehara M, et al. Inhibition of shoot branching by new terpenoid plant hormones. Nature 455. 2008;195-200.e 10:1186.
   Google Scholar
• Gomez-Roldan V, Fermas S, Brewer PB, Puech-Pagès V, Dun EA, Pillot J-P, Letisse F, Matusova R, Danoun S, Portais J-C, et al. Strigolactone inhibition of shoot branching. Nature. 2008;455(7210):189–194. doi:10.1038/nature07271.
   PubMed Web of Science ®Google Scholar
• Ito S, Braguy J, Wang JY, Yoda A, Fiorilli V, Takahashi I, Jamil M, Felemban A, Miyazaki S, Mazzarella T, et al. Canonical strigolactones are not the major determinant of tillering but important rhizospheric signals in rice. Science Advances. 2022;8(44):eadd1278. doi:10.1126/sciadv.add1278.
   PubMed Web of Science ®Google Scholar
• Wakabayashi T, et al. Direct Conversion of Carlactonoic Acid to Orobanchol by Cytochrome P450 CYP722C in Strigolactone Biosynthesis. Science Advances 5 (12): eaax9067. 2019. doi:10.1126/sciadv.aax9067.
   Google Scholar
• Akiyama K, Matsuzaki K-I, Hayashi H. Plant sesquiterpenes induce hyphal branching in arbuscular mycorrhizal fungi. Nature. 2005;435(7043):824–827. doi:10.1038/nature03608.
   PubMed Web of Science ®Google Scholar
• Lanfranco L, Fiorilli V, Venice F, Bonfante P. Strigolactones cross the kingdoms: plants, fungi, and bacteria in the arbuscular mycorrhizal symbiosis. J Exp Bot. 2018;69(9):2175–2188. doi:10.1093/jxb/erx432.
   PubMed Web of Science ®Google Scholar
• Fiorilli V, Wang JY, Bonfante P, Lanfranco L, Al-Babili S. Apocarotenoids: old and new mediators of the arbuscular mycorrhizal symbiosis. Front Plant Sci. 2019;10:1186. doi:10.3389/fpls.2019.01186.
   PubMed Web of Science ®Google Scholar
• Wang JY, Haider I, Jamil M, Fiorilli V, Saito Y, et al. The apocarotenoid metabolite zaxinone regulates growth and strigolactone biosynthesis in rice. Nat Commun. 2019;10:810. doi:10.1038/s41467-019-08461-1.
   PubMed Web of Science ®Google Scholar
• Ablazov A, Mi J, Jamil M, Jia K-P, Wang JY, Feng Q, Al-Babili S. The Apocarotenoid Zaxinone Is a Positive Regulator of Strigolactone and Abscisic Acid Biosynthesis in Arabidopsis Roots. Front Plant Sci. 2020;11:578. doi:10.3389/fpls.2020.00578.
   PubMed Web of Science ®Google Scholar
• Ablazov A, Votta C, Fiorilli V, Wang JY, Aljedaani F, Jamil M, Balakrishna A, Balestrini R, Liew KX, Rajan C, et al. ZAXINONE SYNTHASE 2 regulates growth and arbuscular mycorrhizal symbiosis in rice. Plant Physiol. 2023;191(1):382–399. doi:10.1093/plphys/kiac472.
   PubMed Web of Science ®Google Scholar
• Wang JY, Braguy J, Chen GTE, Jamil M, Balakrishna A, Berqdar L, Al-Babili S. Perspectives on the metabolism of strigolactone rhizospheric signals. Front Plant Sci. 2022a;13:1062107. doi:10.3389/fpls.2022.1062107.
   PubMed Web of Science ®Google Scholar
• Wang JY, Jamil M, Lin P-Y, Ota T, Fiorilli V, Novero M, Zarban RA, Kountche BA, Takahashi I, Martínez C, et al. Efficient mimics for elucidating zaxinone biology and promoting agricultural applications. Mol Plant. 2020;13(11):1654–1661. doi:10.1016/j.molp.2020.08.009.
   PubMed Web of Science ®Google Scholar
• Carbonnel S, Torabi S, Gutjahr C. MAX2 -independent transcriptional responses to rac- GR24 in Lotus japonicus roots. Plant Signal Behav. 2021;16:1. doi:10.1080/15592324.2020.1840852.
   Web of Science ®Google Scholar
• Wang JY, Alseekh S, Xiao T, Ablazov A, Perez de Souza L, Fiorilli V, Anggarani M, Lin P-Y, Votta C, Novero M, et al. Multi-omics approaches explain the growth-promoting effect of the apocarotenoid growth regulator zaxinone in rice. Communications Biology. 2021b;4(1):1222. doi:10.1038/s42003-021-02740-8.
   PubMed Web of Science ®Google Scholar
• Butt H, Jamil M, Wang JY, Al-Babili S, Mahfouz M. Engineering plant architecture via CRISPR/Cas9-mediated alteration of strigolactone biosynthesis. BMC Plant Biol. 2018;18(1):1–9. doi:10.1186/s12870-018-1387-1.
   PubMedGoogle Scholar
• Wang JY, Chen GTE, Jamil M, Braguy J, Sioud S, Liew KX, Balakrishna A, Al-Babili S. Protocol for characterizing strigolactones released by plant roots. STAR Protocols. 2022b;3(2):101352. doi:10.1016/j.xpro.2022.101352.
   PubMedGoogle Scholar
• Proost S, Krawczyk A, Mutwil M. LSTrAP: efficiently combining RNA sequencing data into co-expression networks. BMC Bioinform. 2017;18(1):444. doi:10.1186/s12859-017-1861-z.
   PubMedGoogle Scholar
• Love MI, Huber W, Anders S. Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2. Genome Biol. 2014;15:550. doi:10.1186/s13059-014-0550-8.
   PubMed Web of Science ®Google Scholar