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Tissue-Specific Gene Silencing Mediated by a Naturally Occurring Chalcone Synthase Gene Cluster in Glycine maxW⃞

机译:甘氨酸maxW⃞中天然存在的查耳酮合酶基因簇介导的组织特异性基因沉默

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摘要

Chalcone synthase, a key regulatory enzyme in the flavonoid pathway, constitutes an eight-member gene family in Glycine max (soybean). Three of the chalcone synthase (CHS) gene family members are arranged as inverted repeats in a 10-kb region, corresponding to the I locus (inhibitor). Spontaneous mutations of a dominant allele (I or ii) to a recessive allele (i) have been shown to delete promoter sequences, paradoxically increasing total CHS transcript levels and resulting in black seed coats. However, it is not known which of the gene family members contribute toward pigmentation and how this locus affects CHS expression in other tissues. We investigated the unusual nature of the I locus using four pairs of isogenic lines differing with respect to alleles of the I locus. RNA gel blots using a generic open reading frame CHS probe detected similar CHS transcript levels in stems, roots, leaves, young pods, and cotyledons of the yellow and black isolines but not in the seed coats, which is consistent with the dominant I and ii alleles mediating CHS gene silencing in a tissue-specific manner. Using real-time RT-PCR, a variable pattern of expression of CHS genes in different tissues was demonstrated. However, increase in pigmentation in the black seed coats was associated with release of the silencing effect specifically on CHS7/CHS8, which occurred at all stages of seed coat development. These expression changes were linked to structural changes taking place at the I locus, shown to encompass a much wider region of at least 27 kb, comprising two identical 10.91-kb stretches of CHS gene duplications. The suppressive effect of this 27-kb I locus in a specific tissue of the G. max plant represents a unique endogenous gene silencing mechanism.
机译:黄酮合酶是类黄酮途径中的关键调节酶,在大豆(大豆)中构成了一个八元基因家族。查尔酮合酶(CHS)基因家族中的三个成员以反向重复的形式排列在一个10 kb的区域中,对应于I位点(抑制剂)。显性显性等位基因(I或ii)向隐性等位基因(i)的自发突变已显示删除启动子序列,自相矛盾地增加了总CHS转录水平并导致了黑色种皮。但是,尚不清楚哪个基因家族成员有助于色素沉着,以及该基因座如何影响其他组织中CHS的表达。我们使用关于I基因座的等位基因不同的四对等基因系研究了I基因座的异常性质。使用通用开放阅读框CHS探针的RNA凝胶印迹在黄色和黑色等值线的茎,根,叶,幼荚和子叶中检测到相似的CHS转录水平,但在种皮中未检测到,这与显性I和ii一致等位基因以组织特异性方式介导CHS基因沉默。使用实时RT-PCR,证明了CHS基因在不同组织中表达的可变模式。但是,黑种皮中色素沉着的增加与释放对CHS7 / CHS8的沉默作用有关,这在种皮发育的所有阶段都发生。这些表达变化与在I基因座发生的结构变化有关,显示其包含至少27kb的更宽广的区域,包括两个相同的CHS基因重复的10.91kb延伸。该27-kb I基因座在Max.max植物的特定组织中的抑制作用代表独特的内源基因沉默机制。

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