Olsen O, Wang X, von Wettstein D
Department of Physiology, Carlsberg Laboratory, Copenhagen, Denmark.
Proc Natl Acad Sci U S A. 1993 Sep 1;90(17):8043-7. doi: 10.1073/pnas.90.17.8043.
The molecular basis for the absence of anthocyanins and proanthocyanidins in four independent sodium azide-induced ant18 mutants of barley was examined by sequencing the gene encoding dihydroflavonol 4-reductase in these mutants. Sodium azide generated 21 base substitutions, which corresponds to 0.17% of the 12,704 nucleotides sequenced. Of the substitutions, 86% were nucleotide transitions, and 14% were transversions. A.T-->G.C base pair transitions were about 3 times more frequent than G.C-->A.T transitions. No deletions or mutation hot spots were found. The absence of dihydroflavonol 4-reductase activity in ant18-159, ant18-162, and ant18-164 plants is caused by missense mutations in the respective genes. By using microprojectile bombardment, a plasmid harboring the wild-type Ant18 gene was introduced into ant18-161 mutant cells and resulted in the development of anthocyanin pigmentation, which demonstrates that the mutation is corrected by expression of the introduced gene. On the other hand, a plasmid derivative with the two ant18-161-specific base transitions at the 5' splice site of intron 3 prevented complementation. It is concluded that the absence of detectable mRNA for dihydroflavonol 4-reductase in ant18-161 cells is due to the mutations in the pre-mRNA splice donor site.
通过对大麦四个独立的叠氮化钠诱导的ant18突变体中编码二氢黄酮醇4-还原酶的基因进行测序,研究了这些突变体中花青素和原花青素缺失的分子基础。叠氮化钠产生了21个碱基替换,这相当于所测12,704个核苷酸的0.17%。在这些替换中,86%是核苷酸转换,14%是颠换。A.T→G.C碱基对转换的频率大约是G.C→A.T转换的3倍。未发现缺失或突变热点。ant18 - 159、ant18 - 162和ant18 - 164植株中二氢黄酮醇4-还原酶活性的缺失是由各自基因中的错义突变引起的。通过微弹轰击,将携带野生型Ant18基因的质粒导入ant18 - 161突变体细胞,导致花青素色素沉着的产生,这表明导入基因的表达纠正了突变。另一方面,在第3内含子的5'剪接位点具有两个ant18 - 161特异性碱基转换的质粒衍生物不能互补。得出结论,ant18 - 161细胞中未检测到二氢黄酮醇4-还原酶的mRNA是由于前体mRNA剪接供体位点的突变。