Martin D N, Proebsting W M, Parks T D, Dougherty W G, Lange T, Lewis M J, Gaskin P, Hedden P
Department of Horticulture and Center for Gene Research and Biotechnology, Oregon State University, Corvallis 97331-7304, USA.
Planta. 1996;200(2):159-66. doi: 10.1007/BF00208304.
Treatment of tall and dwarf (3 beta-hydroxylase impaired) genotypes of pea (Pisum sativum L.) with the synthetic, highly active gibberellin (GA), 2,2-dimethyl GA4, reduced the shoot contents of C19-GAs, including GA1, and increased the concentration of the C20-GA, GA19. In shoots of the slender (la crys) mutant, the content of C19-GAs was lower and GA19 content was higher than in those of the tall line. Metabolism of GA19 and GA20 in leaves of a severe (na) GA-deficient dwarf mutant was reduced by GA treatment. The results suggest feed-back regulation of the 20-oxidation and 3 beta-hydroxylation reactions. Feed-back regulation of GA 20-oxidation was studied further using a cloned GA 20-oxidase cDNA from pea. The cDNA, Ps074, was isolated using polymerase chain reaction with degenerate oligonucleotide primers based on pumpkin and Arabidopsis 20-oxidase sequences. After expression of this cDNA clone in Escherichia coli, the product oxidized GA12 to GA15, GA24 and the C19-GA, GA9, which was the major product. The 13-hydroxylated substrate GA53 was similarly oxidized, but less effectively than GA12, giving mainly GA44 with low yields of GA19 and GA20. Ps074 hybridized to polyadenylated RNA from expanding shoots of pea. Amounts of this transcript were less in the slender genotype than in the tall line and were reduced in GA-deficient genotypes by treatment with GA3, suggesting that there is feed-back regulation of GA 20-oxidase gene expression.
用合成的高活性赤霉素(GA)2,2 - 二甲基GA4处理豌豆(Pisum sativum L.)的高株和矮株(3β - 羟化酶受损)基因型,降低了包括GA1在内的C19 - GAs的茎含量,并增加了C20 - GA即GA19的浓度。在细长型(la crys)突变体的茎中,C19 - GAs的含量低于高株系,而GA19的含量则高于高株系。GA处理降低了严重(na)GA缺陷型矮化突变体叶片中GA19和GA20的代谢。结果表明对20 - 氧化和3β - 羟化反应存在反馈调节。利用从豌豆中克隆的GA 20 - 氧化酶cDNA进一步研究了GA 20 - 氧化的反馈调节。基于南瓜和拟南芥20 - 氧化酶序列,使用简并寡核苷酸引物通过聚合酶链反应分离出该cDNA,即Ps074。该cDNA克隆在大肠杆菌中表达后,产物将GA12氧化为GA15、GA24和主要产物C19 - GA即GA9。13 - 羟基化底物GA53也被类似地氧化,但效率低于GA12,主要生成GA44,并以低产率生成GA19和GA20。Ps074与豌豆正在伸展的茎中的聚腺苷酸化RNA杂交。该转录本在细长基因型中的量低于高株系,并且通过GA3处理在GA缺陷基因型中减少,这表明存在对GA 20 - 氧化酶基因表达的反馈调节。