{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,7]],"date-time":"2026-10-07T17:40:58Z","timestamp":1791394858058,"version":"4.3.3"},"reference-count":36,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2008,2,7]],"date-time":"2008-02-07T00:00:00Z","timestamp":1202342400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["The Plant Journal"],"published-print":{"date-parts":[[2008,5]]},"abstract":"<jats:title>Summary<\/jats:title><jats:p>Ultraviolet\u2010B light (UV\u2010B) regulates the expression of genes in a wavelength\u2010 and fluence rate\u2010dependent fashion. A signaling pathway consisting of CONSTITUTIVE PHOTOMORPHOGENESIS\u20031 (COP1) and UV RESISTANCE LOCUS 8 (UVR 8) mediates responsiveness to longer wavelength, low intensity UV\u2010B light\u2010activating, for example, <jats:italic>HY5<\/jats:italic> gene expression. By contrast, transcription of another group of genes, including <jats:italic>ANAC13<\/jats:italic>, modulated by shorter wavelength, higher intensity UV\u2010B is controlled by a yet unknown and largely COP1\u2010independent signaling cascade. Here we provide evidence by promoter deletion analysis, and characterization of genetic mutants displaying aberrant expression patterns, that two cis\u2010regulatory elements, designated MRE<jats:sup><jats:italic>ANAC13<\/jats:italic><\/jats:sup> and UVBox<jats:sup><jats:italic>ANAC13<\/jats:italic><\/jats:sup>, are required for maximal UV\u2010B induction of the <jats:italic>ANAC13<\/jats:italic> gene in transgenic plants. These elements are located in the proximal 150\u2010bp region of the <jats:italic>ANAC13<\/jats:italic> promoter. They show no significant similarity to each other; the putative MRE<jats:sup><jats:italic>ANAC13<\/jats:italic><\/jats:sup> (\u2010AACCTT\u2010) is closely related to MRE<jats:sup><jats:italic>CHS<\/jats:italic><\/jats:sup> (\u2010AACCTA\u2010) found in the <jats:italic>CHALCONE SYNTHASE<\/jats:italic> (<jats:italic>CHS<\/jats:italic>) gene, whereas UVBox<jats:sup><jats:italic>ANAC13<\/jats:italic><\/jats:sup> (with core sequence CAAG) represents a novel cis\u2010regulatory element. The novel UVBox<jats:sup><jats:italic>ANAC13<\/jats:italic><\/jats:sup> sequence is significantly enriched in the promoter region of a subset of UV\u2010B\u2010induced genes with similar activation properties as <jats:italic>ANAC13<\/jats:italic>. In addition, we demonstrate that expression of a chimeric gene containing only the dimerized 12\u2010mer containing UVBox<jats:sup><jats:italic>ANAC13<\/jats:italic><\/jats:sup> fused to a minimal CaMV35S promoter\/luciferase reporter is (i) efficiently induced by shorter wavelength, higher intensity UV\u2010B, but (ii) does not respond either to longer wavelength UV\u2010B and red light or (iii) to abscisic acid treatment and osmotic, salt, heat and cold stresses.<\/jats:p>","DOI":"10.1111\/j.1365-313x.2008.03435.x","type":"journal-article","created":{"date-parts":[[2008,2,7]],"date-time":"2008-02-07T19:03:57Z","timestamp":1202411037000},"page":"402-414","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":50,"title":["Identification of a novel cis\u2010regulatory element for UV\u2010B\u2010induced transcription in 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