Yamaguchi Nobutoshi, Suzuki Mitsuhiro, Fukaki Hidehiro, Morita-Terao Miyo, Tasaka Masao, Komeda Yoshibumi
Laboratory of Plant Science, Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Tokyo, Japan.
Plant Cell Physiol. 2007 Sep;48(9):1275-90. doi: 10.1093/pcp/pcm094. Epub 2007 Jul 24.
The shape of the inflorescence in Arabidopsis thaliana ecotype Columbia is a raceme with individual flowers developing acropetally. The ecotype Landsberg harboring the erecta (er) mutation shows a corymb-like inflorescence, namely a compact inflorescence with a flattened arrangement of flower buds at the tip. To gain insight into inflorescence development, we previously isolated corymb-like inflorescence mutants, named corymbosa1 (crm1), and found that the corymb-like inflorescence in crm1-1 was due to reduced cell elongation of pedicels and stem internodes. Double mutants of crm1 with er and crm2, and crm1-1 crm2-1 er-105 triple mutants show an additive phenotype. crm1-1 is caused by a mutation in BIG, which is required for polar auxin transport. CRM1/BIG is expressed in inflorescence meristems, floral meristems and vascular tissues. We analyzed a collection of 12 reduced lateral root formation (rlr) mutants, which are allelic to crm1-1, and categorized the mutants into three classes, depending on the plant developmental defects. Although all 12 alleles had new stop codons, the phenotype of heterozygous crm1-1/doc1-1 and Northern blotting suggest that new crm1/big mutant alleles are hypomorphic. Auxin-responsive DR5rev::GFP expression was decreased in crm1-1 vasculature of pedicels and stem internodes. PINFORMED1 (PIN1) and CRM1/BIG are expressed in vasculature of pedicels and stem internodes. The severity of corymb-like inflorescence in crm1/big mutants correlated with increased levels of PIN1. Our results suggest that CRM1/BIG controls the elongation of the pedicels and stem internodes through auxin action.
拟南芥生态型哥伦比亚的花序形状为总状花序,单个花朵向顶发育。携带erecta(er)突变的生态型兰茨贝格表现出伞房状花序,即一种紧凑的花序,其顶端的花芽呈扁平排列。为了深入了解花序发育,我们之前分离出了伞房状花序突变体,命名为corymbosa1(crm1),并发现crm1-1中的伞房状花序是由于花梗和茎节间的细胞伸长减少所致。crm1与er和crm2的双突变体,以及crm1-1 crm2-1 er-105三突变体表现出累加表型。crm1-1是由BIG基因突变引起的,BIG是极性生长素运输所必需的。CRM1/BIG在花序分生组织、花分生组织和维管组织中表达。我们分析了12个侧根形成减少(rlr)突变体的集合,这些突变体与crm1-1等位,并根据植物发育缺陷将这些突变体分为三类。尽管所有12个等位基因都有新的终止密码子,但杂合crm1-1/doc1-1的表型和Northern印迹表明,新的crm1/big突变等位基因是亚效等位基因。在crm1-1花梗和茎节间的维管组织中,生长素响应性DR5rev::GFP表达降低。PINFORMED1(PIN1)和CRM1/BIG在花梗和茎节间的维管组织中表达。crm1/big突变体中伞房状花序的严重程度与PIN1水平的增加相关。我们的结果表明,CRM1/BIG通过生长素作用控制花梗和茎节间的伸长。