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MSAP 分析芸薹属 DDM1s 目标序列。

Analysis of target sequences of DDM1s in Brassica rapa by MSAP.

机构信息

Graduate School of Agricultural Science, Tohoku University, 1-1 Tsutsumidori-Amamiyamachi, Aoba-ku, Sendai, Miyagi, 981-8555, Japan.

出版信息

Plant Cell Rep. 2011 Jan;30(1):81-8. doi: 10.1007/s00299-010-0946-1. Epub 2010 Nov 12.

Abstract

DNA methylation is an important epigenetic modification regulating gene expression and transposon silencing. Although epigenetic regulation is involved in some agricultural traits, there has been relatively little research on epigenetic modifications of genes in Brassica rapa, which includes many important vegetables. In B. rapa, orthologs of DDM1, a chromatin remodeling factor required for maintenance of DNA methylation, have been characterized and DNA hypomethylated knock-down plants by RNAi (ddm1-RNAi plants) have been generated. In this study, we investigated differences of DNA methylation status at the genome-wide level between a wild-type (WT) plant and a ddm1-RNAi plant by methylation-sensitive amplification polymorphism (MSAP) analysis. MSAP analysis detected changes of DNA methylation of many repetitive sequences in the ddm1-RNAi plant. Search for body methylated regions in the WT plant revealed no difference in gene body methylation levels between the WT plant and the ddm1-RNAi plant. These results indicate that repetitive sequences are preferentially methylated by DDM1 genes in B. rapa.

摘要

DNA 甲基化是一种重要的表观遗传修饰,调节基因表达和转座子沉默。尽管表观遗传调控涉及一些农业性状,但在包括许多重要蔬菜在内的芸薹属植物中,对基因的表观遗传修饰的研究相对较少。在芸薹属中,已经鉴定了维持 DNA 甲基化所必需的染色质重塑因子 DDM1 的同源物,并且通过 RNAi(ddm1-RNAi 植物)生成了 DNA 低甲基化敲低植物。在这项研究中,我们通过甲基敏感扩增多态性(MSAP)分析研究了野生型(WT)植物和 ddm1-RNAi 植物之间全基因组水平的 DNA 甲基化状态差异。MSAP 分析检测到 ddm1-RNAi 植物中许多重复序列的 DNA 甲基化变化。在 WT 植物中寻找甲基化区域,发现在 WT 植物和 ddm1-RNAi 植物之间基因体甲基化水平没有差异。这些结果表明,重复序列在芸薹属植物中优先被 DDM1 基因甲基化。

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