Robbins Michael L, Sekhon Rajandeep S, Meeley Robert, Chopra Surinder
Department of Crop and Soil Sciences, Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Genetics. 2008 Apr;178(4):1859-74. doi: 10.1534/genetics.107.082503.
The molecular basis of tissue-specific pigmentation of maize carrying a tandemly repeated multicopy allele of pericarp color1 (p1) was examined using Mutator (Mu) transposon-mediated mutagenesis. The P1-wr allele conditions a white or colorless pericarp and a red cob glumes phenotype. However, a Mu-insertion allele, designated as P1-wr-mum6, displayed an altered phenotype that was first noted as occasional red stripes on pericarp tissue. This gain-of-pericarp-pigmentation phenotype was heritable, yielding families that displayed variable penetrance and expressivity. In one fully penetrant family, deep red pericarp pigmentation was observed. Several reports on Mu suppressible alleles have shown that Mu transposons can affect gene expression by mechanisms that depend on transposase activity. Conversely, the P1-wr-mum6 phenotype is not affected by transposase activity. The increased pigmentation was associated with elevated mRNA expression of P1-wr-mum6 copy (or copies) that was uninterrupted by the transposons. Genomic bisulfite sequencing analysis showed that the elevated expression was associated with hypomethylation of a floral-specific enhancer that is approximately 4.7 kb upstream of the Mu1 insertion site and may be proximal to an adjacent repeated copy. We propose that the Mu1 insertion interferes with the DNA methylation and related chromatin packaging of P1-wr, thereby inducing expression from gene copy (or copies) that is otherwise suppressed.
利用Mutator(Mu)转座子介导的诱变技术,研究了携带果皮颜色1(p1)串联重复多拷贝等位基因的玉米组织特异性色素沉着的分子基础。P1-wr等位基因导致果皮白色或无色以及玉米芯颖片红色的表型。然而,一个被命名为P1-wr-mum6的Mu插入等位基因表现出一种改变的表型,最初表现为果皮组织上偶尔出现的红色条纹。这种果皮色素沉着增加的表型是可遗传的,产生了具有可变外显率和表达度的家系。在一个完全外显的家系中,观察到深红色的果皮色素沉着。关于Mu可抑制等位基因的几份报告表明,Mu转座子可以通过依赖转座酶活性的机制影响基因表达。相反,P1-wr-mum6的表型不受转座酶活性的影响。色素沉着增加与未被转座子打断的P1-wr-mum6拷贝的mRNA表达升高有关。基因组亚硫酸氢盐测序分析表明,表达升高与一个花特异性增强子的低甲基化有关,该增强子位于Mu1插入位点上游约4.7 kb处,可能靠近相邻的重复拷贝。我们提出,Mu1插入干扰了P1-wr的DNA甲基化和相关染色质包装,从而诱导了原本被抑制的基因拷贝的表达。