Department of Horticulture, University of Wisconsin-Madison, 1575 Linden Drive, Madison, WI 53706, USA.
Theor Appl Genet. 2013 Jul;126(7):1689-702. doi: 10.1007/s00122-013-2084-y. Epub 2013 Mar 24.
Anthocyanin gene expression has been extensively studied in leaves, fruits and flowers of numerous plants. Little, however, is known about anthocyanin accumulation in roots of carrots or other species. We quantified expression of six anthocyanin biosynthetic genes [phenylalanine ammonia-lyase (PAL3), chalcone synthase (CHS1), flavanone 3-hydroxylase (F3H), dihydroflavonol 4-reductase (DFR1), leucoanthocyanidin dioxygenase (LDOX2), and UDP-glucose:flavonoid 3-O-glucosyltransferase (UFGT)] in three carrot inbreds with contrasting root color: solid purple (phloem and xylem); purple outer phloem/orange xylem; and orange phloem and xylem. Transcripts for five of these genes (CHS1, DFR1, F3H, LDOX2, PAL3) accumulated at high levels in solid purple carrots, less in purple-orange carrot, and low or no transcript in orange carrots. Gene expression coincided with anthocyanin accumulation. In contrast, UFGT expression was comparable in purple and orange carrots and relatively unchanged during root development. In addition, five anthocyanin biosynthesis genes [FLS1 (flavonol synthase), F3H, LDOX2, PAL3, and UFGT] and three anthocyanin transcription factors (DcEFR1, DcMYB3 and DcMYB5) were mapped in a population segregating for the P 1 locus that conditions purple root color. P 1 mapped to chromosome 3 and of the eight anthocyanin biosynthesis genes, only F3H and FLS1 were linked to P 1. The gene expression and mapping data suggest a coordinated regulatory control of anthocyanin expression in carrot root and establish a framework for studying the anthocyanin pathway in carrots, and they also suggest that none of the genes evaluated is a candidate for P 1.
花青素基因的表达在许多植物的叶子、果实和花朵中已经得到了广泛的研究。然而,对于胡萝卜或其他物种的根中花青素的积累知之甚少。我们定量了六个花青素生物合成基因(苯丙氨酸解氨酶(PAL3)、查尔酮合酶(CHS1)、类黄酮 3-羟化酶(F3H)、二氢黄酮醇 4-还原酶(DFR1)、无色花青素双加氧酶(LDOX2)和 UDP-葡萄糖:类黄酮 3-O-葡萄糖基转移酶(UFGT))在三个根颜色不同的胡萝卜自交系中的表达:深紫色(韧皮部和木质部);紫色外韧皮部/橙色木质部;橙色韧皮部和木质部。这五个基因(CHS1、DFR1、F3H、LDOX2、PAL3)的转录物在深紫色胡萝卜中高水平积累,在紫色-橙色胡萝卜中积累较少,在橙色胡萝卜中则低或无转录物。基因表达与花青素积累相吻合。相比之下,UFGT 的表达在紫色和橙色胡萝卜中相似,在根发育过程中相对不变。此外,五个花青素生物合成基因(FLS1(黄酮醇合酶)、F3H、LDOX2、PAL3 和 UFGT)和三个花青素转录因子(DcEFR1、DcMYB3 和 DcMYB5)在一个分离群体中被定位到决定紫色根颜色的 P1 位点。P1 定位在 3 号染色体上,在八个花青素生物合成基因中,只有 F3H 和 FLS1 与 P1 连锁。基因表达和图谱数据表明,胡萝卜根中花青素表达受到协调调控,并为研究胡萝卜中的花青素途径建立了框架,同时也表明,评估的基因中没有一个是 P1 的候选基因。