Burnett R J, Larkins B A
Department of Plant Sciences, University of Arizona, Tucson 85721, USA.
Mol Gen Genet. 1999 Jul;261(6):908-16. doi: 10.1007/s004380051038.
Opaque2 modifier genes cause a two- to three-fold increase in the amount of gamma-zein RNA and protein in maize kernels, and can convert the soft, starchy endosperm of an opaque2 mutant to a hard, vitreous phenotype. We analyzed several aspects of transcriptional and post-transcriptional regulation of gamma-zein gene expression in wild-type, opaque2 and modified opaque2 genotypes to investigate the molecular mechanisms by which opaque2 modifiers influence the expression of gamma-zein genes. We found that the poly(A) tails of the gamma-zein RNAs A and B were of similar length in normal, opaque2 and modified opaque2 genotypes. Multiple poly(A) addition sites were detected for the gamma-zein A and B RNAs, but no evidence was obtained that o2 modifiers influence the selection of these sites. Nucleotide sequence analysis of gamma-zein A and B cDNAs derived from 18-DAP endosperm from normal, opaque2, and modified opaque2 kernels confirmed the use of eight different poly(A) addition sites for gamma-zein A transcripts and six different sites for the gamma-zein B transcripts. It also revealed that the A/B gamma-zein RNA ratio in modified opaque2 was at least 40:1, compared to 1:1 in wild type and 3:1 in opaque2. Nuclear run-on transcription assays showed a dramatic shift in the transcription rate of the gamma-zein A gene relative to the B gene in the modified opaque2 genotype. These results are consistent with a model in which the two opaque2 modifier loci influence gamma-zein gene expression through different mechanisms: one affects transcription of the gamma-zein locus and the other influences the steady state level of gamma-zein RNA.
不透明2修饰基因会使玉米籽粒中γ-醇溶蛋白RNA和蛋白质的含量增加两到三倍,并能将不透明2突变体的柔软、粉质胚乳转变为坚硬、玻璃质的表型。我们分析了野生型、不透明2和修饰的不透明2基因型中γ-醇溶蛋白基因表达的转录和转录后调控的几个方面,以研究不透明2修饰基因影响γ-醇溶蛋白基因表达的分子机制。我们发现,在正常、不透明2和修饰的不透明2基因型中,γ-醇溶蛋白RNA A和B的多聚腺苷酸尾巴长度相似。检测到γ-醇溶蛋白A和B RNA有多个多聚腺苷酸添加位点,但没有证据表明o2修饰基因会影响这些位点的选择。对来自正常、不透明2和修饰的不透明2籽粒18天龄胚乳的γ-醇溶蛋白A和B cDNA进行核苷酸序列分析,证实γ-醇溶蛋白A转录本使用了八个不同的多聚腺苷酸添加位点,γ-醇溶蛋白B转录本使用了六个不同的位点。分析还显示,修饰的不透明2中A/Bγ-醇溶蛋白RNA的比例至少为40:1,而野生型中为1:1,不透明2中为3:1。核转录延伸分析表明,在修饰的不透明2基因型中,γ-醇溶蛋白A基因相对于B基因的转录速率发生了显著变化。这些结果与一个模型一致,即两个不透明2修饰位点通过不同机制影响γ-醇溶蛋白基因表达:一个影响γ-醇溶蛋白位点的转录,另一个影响γ-醇溶蛋白RNA的稳态水平。