互补
突变体
拟南芥
生物
赤霉素
遗传学
荧光素酶
异位表达
基因
转染
作者
Carsten Meier,Thomas Bouquin,Mads Eggert Nielsen,Dora Raventós,Ole Mattsson,Anne B. Rocher,Fritz M. Schomburg,Richard M. Amasino,John Mundy
出处
期刊:Plant Journal
[Wiley]
日期:2001-03-01
卷期号:25 (5): 509-519
被引量:57
标识
DOI:10.1046/j.1365-313x.2001.00980.x
摘要
Summary The gibberellin (GA) 20‐oxidase encoded by Arabidopsis GA5 catalyzes the synthesis of active GAs. GA5 is a regulatory step in GA biosynthesis as GA5 mRNA levels are negatively regulated by its bioactive GA products. A fusion between the GA5 promoter and the firefly luciferase reporter ( GA5 ‐ LUC ) was shown to be similarly regulated, indicating GA feedback of GA5 occurs at the transcriptional level. The fidelity of the GA5 ‐ LUC reporter permitted a fusion genetic screen to identify mutants altered in transgene expression. This bioimaging screen identified two types of recessive mutants with increased LUC activity and apparent GA‐related growth phenotypes, a dwarf ( lue1 ) and two late flowering mutants ( fpa1‐3 and fpa1‐4 ). Mutant progeny exhibited altered levels of LUC and of endogenous GA5 and other GA‐regulated mRNAs. SSLP‐based mapping localized lue1 to chromosome I near the ga2 locus, although complementation analyzes showed that lue1 is not allelic to ga2 . Mapping and complementation analyzes showed that the late flowering mutants are allelic to fpa1 . This provides genetic evidence for crosstalk between the autonomous and gibberellin‐dependent flowering pathways.
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