牵牛花色素沉着与转座因子相关的遗传学和表观遗传学

Shigeru Iida, Yasumasa Morita, Jeong-Doo Choi, Kyeung-Il Park, Atsushi Hoshino
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引用次数: 89

摘要

牵牛花属中,三种牵牛花(日本牵牛花)、紫花牵牛花(常见牵牛花)和三色牵牛花被驯化得很好,并分离出许多具有不同花色素模式的自发突变体。这些自发突变大多是由于在花中花青素色素沉着基因中插入DNA转座元件引起的,其中许多突变呈现出杂色花,如带有色素斑点和扇形的白色花。在这里,我们描述了显示杂色花的突变体的历史背景,并回顾了与这些牵牛花转座因子相关的花色素的遗传和表观遗传调控。I. nil的斑点、斑点、r-1和紫色突变是由Tpnl及其En/Spm超家族的近缘基因Tpn2、Tpn3和Tpn4插入花中花青素着色基因引起的。、DFR-B、CHI、CHS-D、InNHXI。同样,紫花紫豆的片状突变体和粉红色突变体在Ac/Ds超家族中分别有插入CHS-D和F3'H基因的远亲元件Tip100和Tip201。这些转座子的切除频率和时间决定了花的斑驳模式,它们稳定的插入产生素色花,不产生色素斑点或扇形;此外,遗传和表观遗传调控似乎在确定转座子切除的频率和时间方面发挥重要作用。然而,花的杂色并不总是与从花青素色素沉着基因之一的整合DNA转座子的切除有关。三色飞盘花突变体在DFR-B启动子区插入了转座子ItMULE,但在杂色花系中未检测到ItMULE从DFR-B中移除。不稳定的珍珠vrg等位基因。飞碟很可能是一个外等位基因,因为DFR-B启动子中的DNA甲基化似乎与花色素沉着有关。
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Genetics and epigenetics in flower pigmentation associated with transposable elements in morning glories

Among the genus Ipomoea, three morning glories, I. nil the Japanese morning glory), I. purpurea (the common morning glory), and I. tricolor, were domesticated well for floricultural plants, and many spontaneous mutants displaying various flower pigmentation patterns were isolated. Most of these spontaneous mutations were found to be caused by the insertion of DNA transposable elements in the genes for the anthocyanin pigmentation in flowers, and many of them exhibited variegated flowers, such as white flowers with pigmented spots and sectors. Here, we describe the historical background of the mutants displaying variegated flowers and review the genetic and epigenetic regulation in flower pigmentation associated with transposable elements of these morning glories. The flecked, speckled, r-1, and purple mutations in I. nil were caused by insertions of Tpnl and its relatives in the En/Spm superfamily, Tpn2, Tpn3, and Tpn4, into the genes for anthocyanin coloration in flowers,i.e., DFR-B, CHI, CHS-D, and InNHXI, respectively. Similarly, the flaked and pink mutants of I. purpurea have distantly related elements, Tip100 and Tip201, in the Ac/Ds superfamily inserted into the CHS-D and F3'H genes, respectively. The flower variegation patterns can be determined by the frequency and timing of the excision of these transposons, and their stable insertions produce plain color flowers without generating pigmented spots or sectors; furthermore, both genetic and epigenetic regulation appeared to play important roles in determining the frequency and timing of the excision of the transposons. However, flower variegation is not always associated with the excision of an integrated DNA transposon from one of the genes for anthocyanin pigmentation. The mutant Flying Saucers of I. tricolor displaying variegated flowers was found to have the transposon ItMULE inserted into the DFR-B promoter region, but no excision of ITMULEL from the DFR-B could be detected in the variegated flower lines. The instable pearly-vrg allele in cv. Flying Saucers is likely to be an epiallele because the DNA methylation in the DFR-B promoter appeared to be associated with flower pigmentation.

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