Li J, Nam K H, Vafeados D, Chory J
Department of Biology, University of Michigan, Ann Arbor, Michigan 48109-1048, USA.
Plant Physiol. 2001 Sep;127(1):14-22. doi: 10.1104/pp.127.1.14.
Brassinosteroids (BRs) play important roles throughout plant development. Although many genes have been identified that are involved in BR biosynthesis, genetic approaches in Arabidopsis have led to the identification of only one gene, BRI1, that encodes a membrane receptor for BRs. To expand our knowledge of the molecular mechanism(s) of plant steroid signaling, we analyzed many dwarf and semidwarf mutants collected from our previous genetic screens and identified a semidwarf mutant that showed little response to exogenous BR treatments. Genetic analysis of the bin2 (BR-INSENSITIVE 2) mutant indicated that the BR-insensitive dwarf phenotype was due to a semidominant mutation in the BIN2 gene that mapped to the middle of chromosome IV between the markers CH42 and AG. A direct screening for similar semidwarf mutants resulted in the identification of a second allele of the BIN2 gene. Despite some novel phenotypes observed with the bin2/+ mutants, the homozygous bin2 mutants were almost identical to the well-characterized bri1 mutants that are defective in BR perception. In addition to the BR-insensitive dwarf phenotype, bin2 mutants exhibited BR insensitivity when assayed for root growth inhibition and feedback inhibition of CPD gene expression. Furthermore, bin2 mutants displayed an abscisic acid-hypersensitive phenotype that is shared by the bri1 and BR-deficient mutants. A gene dosage experiment using triploid plants suggested that the bin2 phenotypes were likely caused by either neomorphic or hypermorphic gain-of-function mutations in the BIN2 gene. Thus, the two bin2 mutations define a novel genetic locus whose gene product might play a role in BR signaling.
油菜素甾醇(BRs)在植物整个发育过程中发挥着重要作用。尽管已经鉴定出许多参与BR生物合成的基因,但在拟南芥中采用遗传学方法仅鉴定出一个编码BR膜受体的基因BRI1。为了拓展我们对植物甾醇信号传导分子机制的认识,我们分析了从之前的遗传筛选中收集的许多矮化和半矮化突变体,并鉴定出一个对外源BR处理几乎没有反应的半矮化突变体。对bin2(BR不敏感2)突变体的遗传分析表明,BR不敏感的矮化表型是由于BIN2基因中的一个半显性突变所致,该基因定位于第四条染色体中部CH42和AG标记之间。对类似半矮化突变体的直接筛选导致鉴定出BIN2基因的第二个等位基因。尽管在bin2/+突变体中观察到了一些新的表型,但纯合bin2突变体几乎与已充分研究的在BR感知方面有缺陷的bri1突变体相同。除了BR不敏感的矮化表型外,bin2突变体在检测根生长抑制和CPD基因表达的反馈抑制时也表现出BR不敏感性。此外,bin2突变体表现出脱落酸超敏感表型,这与bri1和BR缺陷突变体相同。使用三倍体植物进行的基因剂量实验表明,bin2表型可能是由BIN2基因中的新功能或超功能功能获得性突变引起的。因此,这两个bin2突变定义了一个新的遗传位点,其基因产物可能在BR信号传导中发挥作用。