Schiefelbein J W, Furtek D B, Dooner H K, Nelson O E
Laboratory of Genetics, University of Wisconsin-Madison 53706.
Genetics. 1988 Nov;120(3):767-77. doi: 10.1093/genetics/120.3.767.
The Dissociation (Ds) mutant, Bz-wm, of the maize bronze-1 (bz) locus conditions a leaky phenotype. Plants carrying this mutant allele synthesize a low amount of an altered Bz gene product, which leads to reduced anthocyanin pigmentation in the seed. The molecular analysis reported here shows that the Bz-wm mutant has a 406-bp Ds1 insertion located 63 bp 5' to the start of Bz transcription. Furthermore, the Bz-wm allele contains three additional base pairs within the second exon, relative to the wild-type Bz allele. These additional nucleotides are believed to be derived from the 8-bp target site duplication created by an Activator (Ac) element in a previous allele in the series. The biochemical and molecular analyses of Bz-wm and revertants of Bz-wm indicate that the three additional nucleotides are responsible for the altered enzyme stability, while the Ds1 element affects the steady-state level of Bz-specific protein and RNA. Since the two mutations present in the Bz-wm mutant were each caused by the action of the Ac-Ds transposable element system, these results provide new insights into the ways that transposable elements can modify maize gene expression.
玉米青铜色-1(bz)基因座的解离(Ds)突变体Bz-wm表现出渗漏表型。携带此突变等位基因的植株合成少量改变的Bz基因产物,这导致种子中花青素色素沉着减少。本文报道的分子分析表明,Bz-wm突变体在Bz转录起始位点上游63 bp处有一个406 bp的Ds1插入。此外,相对于野生型Bz等位基因,Bz-wm等位基因在第二个外显子内还包含三个额外的碱基对。这些额外的核苷酸被认为源自该系列中前一个等位基因中由激活子(Ac)元件产生的8 bp靶位点重复。对Bz-wm及其回复体的生化和分子分析表明,这三个额外的核苷酸导致了酶稳定性的改变,而Ds1元件影响Bz特异性蛋白质和RNA的稳态水平。由于Bz-wm突变体中存在的两个突变均由Ac-Ds转座子元件系统的作用引起,这些结果为转座子修饰玉米基因表达的方式提供了新的见解。