首页> 外文期刊>Theoretical and Applied Genetics >An allele of dihydroflavonol 4-reductase associated with the ability to produce red anthocyanin pigments in potato (Solanum tuberosum L.)
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An allele of dihydroflavonol 4-reductase associated with the ability to produce red anthocyanin pigments in potato (Solanum tuberosum L.)

机译:二氢黄酮醇4-还原酶的等位基因,与马铃薯(Solanum tuberosum L.)产生红色花色苷色素的能力有关

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The potato R locus is necessary for the production of red pelargonidin-based anthocyanin pigments in any tissue of the plant, including tuber skin and flower petals. The production of pelargonidins in plants requires the activity of dihydroflavonol 4-reductase (DFR) to catalyze the reduction of dihydrokaempferol into leucopelargonidin. To test the hypothesis that potato R encodes DFR, portions of both dfr alleles were sequenced from a diploid potato clone known to be heterozygous Rr. Sequence comparison revealed a polymorphic BamHI restriction site. The presence or absence of this site was monitored in three diploid populations that segregated for R, as well as in a wide range of tetraploid breeding clones and cultivars, by amplifying a fragment of dfr and digesting the products with BamHI. An identically sized dfr restriction fragment lacking the BamHI site was present in all potato clones that produced red anthocyanin pigments, while the same fragment was absent in many potato clones with white tuber skin and flowers. An independent RFLP test using DraI to detect sequence polymorphism was performed on a subset of the potato clones. This test also revealed dfr-derived bands that were present in all red-colored potatoes and absent in several white clones. The presence of shared restriction fragments in all red-colored potatoes provides strong evidence that R does indeed code for DFR. The data are also consistent with a 48 year-old hypothesis by Dodds and Long, that R was selected just once during the domestication of potato. A cDNA clone corresponding to the red allele of dfr was sequenced and compared to two other alleles. The red allele is predicted to encode a 382 amino acid protein that differs at ten amino acid positions from the gene products of the two alternative alleles. Several of these differences map in a region known to influence DFR substrate specificity in Gerbera.
机译:马铃薯R基因座是在植物的任何组织(包括块茎皮和花瓣)中生产基于红色pelargonidin的花色苷色素所必需的。植物中pelargonidins的产生需要二氢黄酮醇4-还原酶(DFR)的活性,以催化将dihydrokaempferol还原为leucopelargonidin。为了检验马铃薯R编码DFR的假设,从已知为杂合Rr的二倍体马铃薯克隆中测序了两个dfr等位基因的部分。序列比较显示多态性BamHI限制性酶切位点。通过扩增dfr片段并用BamHI消化产物,在三个R分离的二倍体群体以及广泛的四倍体育种克隆和品种中监测该位点的存在与否。在所有产生红色花色苷色素的马铃薯克隆中都存在一个缺少BamHI位点的大小相同的dfr限制性片段,而在许多块茎皮肤和花呈白色的马铃薯克隆中却没有相同的片段。对马铃薯克隆的一个子集进行了使用DraI检测序列多态性的独立RFLP测试。该测试还揭示了在所有红色马铃薯中均存在的dfr衍生条带,在几个白色克隆中却不存在这些条带。所有红色马铃薯中共有限制性片段的存在提供了有力证据,证明R确实编码DFR。数据也与Dodds和Long的48年假说相符,即R在马铃薯驯化过程中仅被选择一次。对与dfr的红色等位基因相对应的cDNA克隆进行测序,并与其他两个等位基因进行比较。预测红色等位基因编码一个382个氨基酸的蛋白质,该蛋白质与两个其他等位基因的基因产物在十个氨基酸位置处不同。这些差异中的几个位于已知会影响非洲菊中DFR底物特异性的区域。

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