Iwate Biotechnology Research Center, 22-174-4, Narita, Kitakami, Iwate, 024-0003, Japan.
Mol Genet Genomics. 2011 Dec;286(5-6):371-82. doi: 10.1007/s00438-011-0652-x. Epub 2011 Oct 15.
We investigated the genetic basis for the derivation of pink coloration in petals from blue flowers in cultivated gentians. Using a revertant blue-flower phenotype that arose spontaneously from a pink-flowered cultivar, we sought to elucidate the molecular mechanism of flower color restoration caused by a suppressor mutation. Detailed sequencing analysis identified three novel deficient flavonoid 3',5'-hydroxylase (F3'5'H) alleles in pink-flowered gentians in addition to two mutations identified previously (Nakatsuka et al. in Mol Genet Genomics 275:231-241, 2006). Among the deficient alleles, one allele that contained a novel miniature inverted-repeat transposable element (GtMITE1) insertion in an intron of F3'5'H was shown to cause missplicing, resulting in abnormal F3'5'H transcripts and the pink-flower phenotype. The other two mutations were identified as a single-nucleotide insertion and gypsy-Ty3 retrotransposon (Tgt1) insertion within exon 1 and exon 2 of the F3'5'H gene, respectively. The blue-flowered revertant mutant contained a single-nucleotide spontaneous mutation immediately 3' of the TAA target site duplication and the GtMITE1 insertion, which caused restoration of normal splicing of F3'5'H and the normal blue-flower phenotype. Transient expression assays in gentian flowers in vivo demonstrated that normal F3'5'H splicing pattern was recovered from missplicing induced by the GtMITE1 insertion by the single-nucleotide substitution. These findings extend our knowledge of genomic evolution by transposable elements and spontaneous mutations in Gentiana species of economic and medical importance.
我们研究了栽培龙胆属植物中花瓣由蓝色变为粉红色的遗传基础。利用自发产生于粉红色品种的蓝色复花表型,我们试图阐明由抑制突变引起的花颜色恢复的分子机制。详细的测序分析除了先前鉴定的两个突变(Nakatsuka 等人,Mol Genet Genomics 275:231-241, 2006)外,还在粉红色的龙胆属植物中鉴定了三个新的缺失类黄酮 3',5'-羟化酶(F3'5'H)等位基因。在缺失的等位基因中,一个等位基因在 F3'5'H 的内含子中含有一个新的微型反向重复转座元件(GtMITE1)插入,导致异常剪接,产生异常的 F3'5'H 转录本和粉红色表型。另外两个突变分别鉴定为 F3'5'H 基因外显子 1 和外显子 2 中的单核苷酸插入和gypsy-Ty3 反转录转座子(Tgt1)插入。蓝色复花突变体在 TAA 靶标重复和 GtMITE1 插入的 3'末端含有一个单核苷酸自发突变,导致 F3'5'H 正常剪接和正常蓝色花表型的恢复。在龙胆属植物体内的瞬时表达试验表明,通过单核苷酸取代可以从 GtMITE1 插入诱导的异常剪接中恢复正常的 F3'5'H 剪接模式。这些发现扩展了我们对经济和医学重要的龙胆属物种中转座元件和自发突变引起的基因组进化的认识。