Laboratories of Plant Breeding, Research Faculty of Agriculture, Hokkaido University, Sapporo 060-8589, Japan.
Plant Physiol. 2009 Nov;151(3):1557-69. doi: 10.1104/pp.109.142356. Epub 2009 Sep 16.
Transposon insertions occasionally occur in the promoter regions of plant genes, many of which are still capable of being transcribed. However, it remains unclear how transcription of such promoters is able to occur. Insertion of the Tam3 transposon into various genes of Antirrhinum majus can confer leaky phenotypes without its excision. These genes, named Tam3-permissible alleles, often contain Tam3 in their promoter regions. Two alleles at different anthocyanin biosynthesis loci, nivea(recurrensTam3) (niv(rec)) and pallida(recurrensTam3) (pal(rec)), both contain Tam3 at a similar position immediately upstream of the promoter TATA-box; however, these insertions had different phenotypic consequences. Under conditions where the inserted Tam3 is immobilized, the niv(rec) line produces pale red petals, whereas the pal(rec) line produces no pigment. These pigmentation patterns are correlated with the level of transcripts from the niv(rec) or pal(rec) alleles, and these transcriptional activities are independent of DNA methylation in their promoter regions. In niv(rec), Tam3 is inserted in an orientation that results in the 3' end of Tam3 adjacent to the 5' region of the gene coding sequence. In contrast, the pal(rec) allele contains a Tam3 insertion in the opposite orientation. Four of five different nonrelated genes that are also Tam3-permissible alleles and contain Tam3 within the promoter region share the same Tam3 orientation as niv(rec). The different transcriptional activities dependent on Tam3 orientation in the Antirrhinum promoters were consistent with expression of luciferase reporter constructs introduced into yeast chromosomes but not with transient expression of these constructs in Antirrhinum cells. These results suggest that for Tam3 to sustain stable transcriptional activity in various promoters it must be embedded in chromatin.
转座子插入偶尔发生在植物基因的启动子区域,其中许多仍然能够被转录。然而,目前尚不清楚这些启动子的转录是如何发生的。Tam3 转座子插入金鱼草的各种基因中,即使没有切除,也能赋予渗漏表型。这些基因被命名为 Tam3 允许等位基因,它们的启动子区域通常含有 Tam3。在不同的花色素生物合成基因座上的两个等位基因,nivea(recurrensTam3)(niv(rec))和 pallida(recurrensTam3)(pal(rec)),都在启动子 TATA 框的上游类似位置含有 Tam3;然而,这些插入具有不同的表型后果。在插入的 Tam3 被固定的情况下,niv(rec)系产生淡红色花瓣,而 pal(rec)系则不产生色素。这些色素沉着模式与来自 niv(rec)或 pal(rec)等位基因的转录本水平相关,并且这些转录活性与它们启动子区域的 DNA 甲基化无关。在 niv(rec)中,Tam3 以插入的方向导致 Tam3 的 3' 末端与基因编码序列的 5' 区域相邻。相比之下,pal(rec)等位基因含有相反方向的 Tam3 插入。在同样含有 Tam3 位于启动子区域的五个不同的、非相关基因中,有四个基因具有与 niv(rec)相同的 Tam3 取向。在金鱼草启动子中,Tam3 取向依赖性的不同转录活性与酵母染色体中引入的荧光素酶报告基因构建体的表达一致,但与这些构建体在金鱼草细胞中的瞬时表达不一致。这些结果表明,为了使 Tam3 在各种启动子中维持稳定的转录活性,它必须嵌入染色质中。