Rameau Catherine, Murfet Ian C, Laucou Valerie, Floyd Robert S, Morris Suzanne E, Beveridge Christine A
Station de Genetique et d'Amelioration des Plantes, INRA, Route de St-Cyr, F-78026 Versailles, France School of Plant Science, University of Tasmania, GPO Box 252-55, Hobart TAS 7001, Australia Department of Botany, University of Queensland, Brisbane QLD 4072, Australia.
Physiol Plant. 2002 Jul;115(3):458-467. doi: 10.1034/j.1399-3054.2002.1150316.x.
Our studies on two branching mutants of pea (Pisum sativum L.) have identified a further Ramosus locus, Rms6, with two recessive or partially recessive mutant alleles: rms6-1 (type line S2-271) and rms6-2 (type line K586). Mutants rms6-1 and rms6-2 were derived from dwarf and tall cultivars, Solara and Torsdag, respectively. The rms6 mutants are characterized by increased branching from basal nodes. In contrast, mutants rms1 through rms5 have increased branching from both basal and aerial (upper stem) nodes. Buds at the cotyledonary node of wild-type (WT) plants remain dormant but in rms6 plants these buds were usually released from dormancy. Their growth was either subsequently inhibited, sometimes even prior to emergence above ground, or they grew into secondary stems. The mutant phenotype was strongest for rms6-1 on the dwarf background. Although rms6-2 had a weak single-mutant phenotype, the rms3-1 rms6-2 double mutant showed clear transgression and an additive branching phenotype, with a total lateral length almost 2-fold greater than rms3-1 and nearly 5-fold greater than rms6-2. Grafting studies between WT and rms6-1 plants demonstrated the primary action of Rms6 may be confined to the shoot. Young WT and rms6-1 shoots had similar auxin levels, and decapitated plants had a similar magnitude of response to applied auxin. Abscisic acid levels were elevated 2-fold at node 2 of young rms6-1 plants. The Rms6 locus mapped to the R to Gp segment of linkage group V (chromosome 3). The rms6 mutants will be useful for basic research and also have possible agronomical value.
我们对豌豆(Pisum sativum L.)的两个分枝突变体进行的研究,确定了一个新的Ramosus基因座Rms6,它有两个隐性或部分隐性突变等位基因:rms6-1(类型系S2-271)和rms6-2(类型系K586)。突变体rms6-1和rms6-2分别源自矮化品种索拉拉(Solara)和高秆品种托尔斯达格(Torsdag)。rms6突变体的特征是基部节位的分枝增加。相比之下,rms1至rms5突变体基部和地上部(上部茎)节位的分枝均增加。野生型(WT)植株子叶节的芽保持休眠状态,但在rms6植株中,这些芽通常会打破休眠。其生长随后要么受到抑制,有时甚至在出土之前,要么长成次生茎。在矮化背景下,rms6-1的突变表型最强。尽管rms6-2的单突变表型较弱,但rms3-1 rms6-2双突变体表现出明显的超亲分离和累加的分枝表型,总侧枝长度几乎是rms3-1的2倍,是rms6-2的近5倍。WT和rms6-1植株之间的嫁接研究表明,Rms6的主要作用可能局限于地上部分。WT和rms6-1的幼嫩地上部分生长素水平相似,去顶植株对施用生长素的反应幅度也相似。在rms6-1幼嫩植株的第2节位,脱落酸水平升高了2倍。Rms6基因座定位于连锁群V(第3号染色体)的R至Gp区段。rms6突变体将有助于基础研究,也可能具有农艺价值。