Campanella J J, Ludwig-Mueller J, Town C D
Department of Biology, Case Western Reserve University, Cleveland, Ohio 44106, USA.
Plant Physiol. 1996 Oct;112(2):735-45. doi: 10.1104/pp.112.2.735.
Two mutants of Arabidopsis thaliana that are resistant to growth inhibition by indole-3-acetic acid (IAA)-phenylalanine have been isolated. Both mutants were 2- to 3-fold more resistant than wild type to inhibition by IAA-phenylalanine, IAA-alanine, and IAA-glycine in root growth assays. The mutant icr1 (but not icr2) also shows some resistance to IAA-aspartate. Studies using 3H-labeled IAA-phenylalanine showed that the uptake of conjugate from the medium by icr1 was the same as wild type and was reduced by about 25% in icr2. No differences in hydrolysis of the exogenous conjugate were detected between the mutants and their wild-type parents. There was no significant metabolism of the IAA released from the [3H]IAA-phenylalanine, whereas exogenous [3H]IAA was rapidly metabolized to two unidentified products considerably more polar than IAA. Analysis of a cross between icr1 and icr2 indicated that these mutations were at distinct loci and that their effects were additive, and preliminary mapping data indicated that icr1 and icr2 were located at the top and bottom of chromosome V, respectively.
已分离出拟南芥的两个对吲哚 - 3 - 乙酸(IAA) - 苯丙氨酸生长抑制具有抗性的突变体。在根生长试验中,两个突变体对IAA - 苯丙氨酸、IAA - 丙氨酸和IAA - 甘氨酸抑制的抗性均比野生型高2至3倍。突变体icr1(而非icr2)对IAA - 天冬氨酸也表现出一定抗性。使用³H标记的IAA - 苯丙氨酸进行的研究表明,icr1从培养基中摄取共轭物的情况与野生型相同,而icr2摄取量减少约25%。在突变体与其野生型亲本之间未检测到外源共轭物水解的差异。从[³H]IAA - 苯丙氨酸释放的IAA没有显著代谢,而外源[³H]IAA迅速代谢为两种极性比IAA大得多的未知产物。对icr1和icr2之间杂交的分析表明,这些突变位于不同位点且其效应是累加的,初步定位数据表明icr1和icr2分别位于第V染色体的顶部和底部。