Department of Biology, University of California, Los Angeles, CA 90024.
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9031-5. doi: 10.1073/pnas.85.23.9031.
The endogenous gibberellins (GAs) were examined from young vegetative shoots of the dominant mutant, Dwarf-8, a GA-nonresponder, and normal maize; GA(44), GA(17), GA(19), GA(20), GA(29), GA(1), and GA(8), members of the early-13-hydroxylation pathway, were identified from both kinds of shoots by full-scan mass spectra and Kovats retention indices. In addition, we report the identification of 3-epi-GA(1), GA(3), GA(4), GA(5), GA(7), GA(9), GA(12), GA(15), GA(24), GA(34), and GA(53) by using the same criteria. [1,7,12,18-(14)C(4)]GA(53) and -GA(44), [17-(2)H(2)]GA(19), and [17-(13)C,(3)H(2)]GA(20), -GA(29), -GA(1), -GA(8), and -GA(5) were used as internal standards to determine the endogenous levels of these GAs by measurement of isotope dilution, using capillary gas chromatography and selected ion monitoring. Shoots of Dwarf-8 accumulate relatively high levels of GA(20), GA(1), and GA(8). The accumulation of GA(1) appears to be related to gene dosage. Since Dwarf-8 contains the same pattern of GAs as normals (including GA(1) and GA(3)), the genetic control point probably lies after GA(1) (and GA(3)). Thus Dwarf-8 may be a GA receptor mutant or a mutant that controls a product downstream from the binding of the bioactive GA to a receptor.
内源赤霉素(GAs)从优势突变体矮化 8 号的幼嫩营养枝和正常玉米中进行了检测;通过全扫描质谱和柯瓦茨保留指数,从这两种枝中鉴定出了属于早期 13-羟化途径的 GA(44)、GA(17)、GA(19)、GA(20)、GA(29)、GA(1)和 GA(8);此外,我们还通过相同的标准鉴定出了 3-表赤霉素(GA(3))、GA(4)、GA(5)、GA(7)、GA(9)、GA(12)、GA(15)、GA(24)、GA(34)和 GA(53)。[1,7,12,18-(14)C(4)]GA(53)和-GA(44)、[17-(2)H(2)]GA(19)以及[17-(13)C,(3)H(2)]GA(20)、-GA(29)、-GA(1)、-GA(8)和 -GA(5)被用作内标,通过毛细管气相色谱和选择离子监测,用同位素稀释法测定这些 GA 的内源性水平。矮化 8 号的枝中积累了相对较高水平的 GA(20)、GA(1)和 GA(8)。GA(1)的积累似乎与基因剂量有关。由于矮化 8 号含有与正常玉米相同的 GA 模式(包括 GA(1)和 GA(3)),因此遗传控制点可能位于 GA(1)(和 GA(3))之后。因此,矮化 8 号可能是赤霉素受体突变体或控制生物活性 GA 与受体结合后产物的突变体。