一种托伦尼亚(托伦尼亚)。Fourn交货)。通过将DNA转座子插入R2R3-MYB基因,新突变体“Flecked”产生杂色花

T. Nishijima, Yasumasa Morita, K. Sasaki, M. Nakayama, H. Yamaguchi, N. Ohtsubo, T. Niki, T. Niki
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引用次数: 20

摘要

一种新的托伦尼亚病(托伦尼亚病)。(见Fourn.)突变体' flecked ',它有杂色的花,是从甲基磺酸乙酯处理的M2植株中获得的。这个突变体的下唇有浅紫色背景的小紫色斑点,而正常型的下唇是纯紫色。突变性状经常恢复为半圆形紫色扇形或实心紫色下唇。具有实心紫罗兰下唇的萌发逆转录植株也经常出现在自花授粉突变体S1植株中。突变型下唇花青素含量明显低于正常型。这是由于编码花青素生物合成酶的基因表达减少,这些生物合成酶包括:torenia查尔酮合成酶(TfCHS)、黄酮3羟化酶(TfF3H)、二氢黄酮醇4-还原酶(TfDFR)、花青素合成酶(TfANS)和udp -葡萄糖3- o类黄酮葡萄糖基转移酶(TfUFGT)。在突变体的下唇,编码R2R3MYB转录因子的基因(TfMYB1, Torenia fournieri MYB1)的表达量远低于正常型和逆转型;这是由于在TfMYB1的第二个内含子中插入了一个增强子/抑制子-突变子(En/Spm)样转座子(Ttf1, Torenia fournieri转座子1)。此外,研究发现,下唇花青素积累的逆转与TfMYB1中Ttf1的切除有关。在torenia中,TfMYB1的过表达导致上述五个结构基因的表达增强,从而导致紫色愈伤组织中花青素的积累,表明TfMYB1调节了这些基因。因此,我们得出结论,ttf1插入的TfMYB1的纯合等位基因导致了突变表型。Ttf1是一个非自主元件,因为Ttf1没有编码转座酶的DNA序列。基于这些结果,讨论了斑点突变体在torenia育种和转座子标记方面的潜在用途。
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A Torenia (Torenia fournieri Lind. ex Fourn.) Novel Mutant 'Flecked' Produces Variegated Flowers by Insertion of a DNA Transposon into an R2R3-MYB Gene
A novel torenia (Torenia fournieri Lind. ex Fourn.) mutant ‘flecked’, which bears variegated flowers, was obtained from ethyl methanesulfonate-treated M2 plants. The lower lip of this mutant has small violet spots with a pale violet background, while that of the normal type is solid violet. The mutant trait frequently reverted to a semicircular violet sector or solid violet lower lip. Germinal revertant plants with a solid violet lower lip also frequently occurred in S1 plants derived from self-pollinated mutant flowers. In the lower lip of the mutant type, anthocyanin concentration was much lower than in the normal type. This was attributed to decreased expression of the genes encoding anthocyanin biosynthesis enzymes, i.e. torenia chalcone synthase (TfCHS), flavanone 3hydroxylase (TfF3H), dihydroflavonol 4-reductase (TfDFR), anthocyanidin synthase (TfANS), and UDP-glucose 3-O-flavonoid glucosyltransferase (TfUFGT). In the lower lip of the mutant, expression of a gene encoding R2R3MYB transcription factor (TfMYB1, Torenia fournieri MYB1) was much lower than in the normal type and the revertants; this was caused by insertion of a Enhancer/Suppressor-Mutator (En/Spm)-like transposon (Ttf1, Transposon Torenia fournieri 1) in the 2nd intron of TfMYB1. Furthermore, it was found that the reversion of anthocyanin accumulation in the lower lips correlated to excision of Ttf1 from the TfMYB1. Overexpression of TfMYB1 in torenia caused anthocyanins to accumulate in the purple callus as a result of enhanced expression of the five structural genes mentioned above, demonstrating that TfMYB1 regulates these genes. Therefore, we concluded that a homozygous allele of Ttf1-inserted TfMYB1 caused the mutant phenotype. Ttf1 is a nonautonomous element because Ttf1 does not have the DNA sequence encoding transposase. Based on these results, potential uses of the flecked mutant for torenia breeding and transposon tagging are discussed.
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