Flavell R B, O'Dell M
John Innes Institute, John Innes Centre for Plant Science Research, Norwich, UK.
Dev Suppl. 1990:15-20.
Chromosome marking by cytosine methylation has been examined in two gene systems in wheat--at the loci encoding high molecular weight (HMW) glutenin subunits (seed proteins) and ribosomal RNA. Variation in cytosine methylation occurs between progeny in highly inbred lines around the HMW glutenin locus. The variation is inherited through meiosis to F1 and F2 generations but occasionally a new variant arises. Specific cytosine residues lose their methyl group in the seed, the organ where the genes are expressed. Within the multigene family of ribosomal RNA genes, several subsets of genes can be defined based upon the cytosine methylation patterns. High activity of a ribosomal RNA gene locus is correlated with loss of methylation at specific cytosine residues, especially in the promoter and upstream regulatory regions. A model is described in which the subset of genes selected to be used are those to which specific regulatory proteins and transcription complexes bind most favourably. Binding of such proteins inhibits cytosine methylation and so marks the subset of genes for expression in subsequent cell generations. Examples are described where new types of RNA genes are introduced via sexual crosses that result in changes to the methylation patterns of the ribosomal RNA genes. The processes determining the changes begin, it is believed, in the fertilised egg.
已在小麦的两个基因系统中研究了通过胞嘧啶甲基化进行的染色体标记——在编码高分子量(HMW)谷蛋白亚基(种子蛋白)的基因座和核糖体RNA基因座。在高度自交系的后代中,HMW谷蛋白基因座周围的胞嘧啶甲基化存在变异。这种变异通过减数分裂遗传给F1和F2代,但偶尔会出现新的变异体。特定的胞嘧啶残基在种子(即基因表达的器官)中失去其甲基基团。在核糖体RNA基因的多基因家族中,可以根据胞嘧啶甲基化模式定义几个基因子集。核糖体RNA基因座的高活性与特定胞嘧啶残基的甲基化缺失相关,尤其是在启动子和上游调控区域。本文描述了一个模型,其中被选择使用的基因子集是那些与特定调控蛋白和转录复合物结合最有利的基因。此类蛋白的结合会抑制胞嘧啶甲基化,从而标记出在后续细胞世代中表达的基因子集。文中还描述了一些例子,通过有性杂交引入新型RNA基因,导致核糖体RNA基因甲基化模式发生变化。据信,决定这些变化的过程始于受精卵。