Scheffler B, Franken P, Schütt E, Schrell A, Saedler H, Wienand U
Max-Planck-Institut für Züchtungsforschung, Köln, Germany.
Mol Gen Genet. 1994 Jan;242(1):40-8. doi: 10.1007/BF00277346.
The structure and function of several C1 alleles have been investigated molecularly and the importance of C1 promoter sequences for gene expression was studied using transient transformation assays. The C1 mutants analyzed were the overexpressing allele C1-S, the light-inducible allele c1-p, the null recessive allele c1-n, and the Ds element-induced allele c1-m1. Nucleotide sequence analysis of the alleles revealed a number of differences, predominantly located at the 3' end of the gene. The promoter sequences of the C1 alleles investigated so far (including wild-type and the dominant inhibitor C1-I allele) are almost identical except for two short footprint-like sequences (Box I and Box II) close to the putative CAAT box. Northern blot experiments and transient expression in particle gun experiments indicate that these sequences may be correlated with the different expression patterns of the alleles in the aleurone of maturing and germinating kernels.
已经从分子水平上研究了几个C1等位基因的结构和功能,并使用瞬时转化试验研究了C1启动子序列对基因表达的重要性。所分析的C1突变体包括过表达等位基因C1-S、光诱导等位基因c1-p、无效隐性等位基因c1-n和Ds元件诱导的等位基因c1-m1。这些等位基因的核苷酸序列分析揭示了许多差异,主要位于基因的3'端。到目前为止所研究的C1等位基因(包括野生型和显性抑制因子C1-I等位基因)的启动子序列几乎相同,只是在靠近假定CAAT框的两个短的足迹样序列(框I和框II)处有所不同。Northern杂交实验和粒子枪实验中的瞬时表达表明,这些序列可能与成熟和发芽籽粒糊粉层中等位基因的不同表达模式相关。