Fernandez Donna E, Wang Chieh-Ting, Zheng Yumei, Adamczyk Benjamin J, Singhal Rajneesh, Hall Pamela K, Perry Sharyn E
Department of Botany, University of Wisconsin, Madison, Wisconsin 53706 (D.E.F., C.-T.W., B.J.A., R.S., P.K.H.); andDepartment of Plant and Soil Sciences, University of Kentucky, Lexington, Kentucky 40546 (Y.Z., S.E.P.)
Department of Botany, University of Wisconsin, Madison, Wisconsin 53706 (D.E.F., C.-T.W., B.J.A., R.S., P.K.H.); andDepartment of Plant and Soil Sciences, University of Kentucky, Lexington, Kentucky 40546 (Y.Z., S.E.P.).
Plant Physiol. 2014 Aug;165(4):1591-1603. doi: 10.1104/pp.114.242990. Epub 2014 Jun 19.
Multiple factors, including the MADS-domain proteins AGAMOUS-LIKE15 (AGL15) and AGL18, contribute to the regulation of the transition from vegetative to reproductive growth. AGL15 and AGL18 were previously shown to act redundantly as floral repressors and upstream of FLOWERING LOCUS T (FT) in Arabidopsis (Arabidopsis thaliana). A series of genetic and molecular experiments, primarily focused on AGL15, was performed to more clearly define their role. agl15 agl18 mutations fail to suppress ft mutations but show additive interactions with short vegetative phase (svp) mutations in ft and suppressor of constans1 (soc1) backgrounds. Chromatin immunoprecipitation analyses with AGL15-specific antibodies indicate that AGL15 binds directly to the FT locus at sites that partially overlap those bound by SVP and FLOWERING LOCUS C. In addition, expression of AGL15 in the phloem effectively restores wild-type flowering times in agl15 agl18 mutants. When agl15 agl18 mutations are combined with agl24 svp mutations, the plants show upward curling of rosette and cauline leaves, in addition to early flowering. The change in leaf morphology is associated with elevated levels of FT and ectopic expression of SEPALLATA3 (SEP3), leading to ectopic expression of floral genes. Leaf curling is suppressed by sep3 and ft mutations and enhanced by soc1 mutations. Thus, AGL15 and AGL18, along with SVP and AGL24, are necessary to block initiation of floral programs in vegetative organs.
包括MADS结构域蛋白AGAMOUS-LIKE15(AGL15)和AGL18在内的多种因素,参与调控从营养生长到生殖生长的转变。先前研究表明,AGL15和AGL18在拟南芥中作为花抑制因子发挥冗余作用,且位于开花位点T(FT)的上游。为了更清楚地界定它们的作用,进行了一系列主要聚焦于AGL15的遗传和分子实验。agl15 agl18突变无法抑制ft突变,但在ft和CONSTANS1抑制因子(soc1)背景下,与短营养期(svp)突变表现出累加互作。用AGL15特异性抗体进行的染色质免疫沉淀分析表明,AGL15直接结合在FT基因座上,其结合位点与SVP和开花位点C(FLOWERING LOCUS C)的结合位点部分重叠。此外,在韧皮部中表达AGL15能有效恢复agl15 agl18突变体的野生型开花时间。当agl15 agl18突变与agl24 svp突变结合时,除了早花外,植株还表现出莲座叶和茎生叶向上卷曲。叶片形态的变化与FT水平升高和SEPALLATA3(SEP3)异位表达有关,导致花基因的异位表达。sep3和ft突变可抑制叶片卷曲,而soc1突变则增强叶片卷曲。因此,AGL15和AGL18与SVP和AGL24一起,对于阻止营养器官中花程序的启动是必需的。