Papa C M, Springer N M, Muszynski M G, Meeley R, Kaeppler S M
Department of Agronomy, University of Wisconsin-Madison, 1575 Linden Drive, Madison, Wisconsin 53706, USA.
Plant Cell. 2001 Aug;13(8):1919-28. doi: 10.1105/tpc.010064.
A cytosine DNA methyltransferase containing a chromodomain, Zea methyltransferase2 (Zmet2), was cloned from maize. The sequence of ZMET2 is similar to that of the Arabidopsis chromomethylases CMT1 and CMT3, with C-terminal motifs characteristic of eukaryotic and prokaryotic DNA methyltransferases. We used a reverse genetics approach to determine the function of the Zmet2 gene. Plants homozygous for a Mutator transposable element insertion into motif IX had a 13% reduction in methylated cytosines. DNA gel blot analysis of these plants with methylation-sensitive restriction enzymes and bisulfite sequencing of a 180-bp knob sequence showed reduced methylation only at CpNpG sites. No reductions in methylation were observed at CpG or asymmetric sites in heterozygous or homozygous mutant plants. Our research shows that chromomethylase Zmet2 is required for in vivo methylation of CpNpG sequences.
从玉米中克隆出一种含有色域的胞嘧啶DNA甲基转移酶,即玉米甲基转移酶2(Zmet2)。ZMET2的序列与拟南芥色域甲基化酶CMT1和CMT3的序列相似,其C端基序具有真核和原核DNA甲基转移酶的特征。我们采用反向遗传学方法来确定Zmet2基因的功能。因Mutator转座元件插入基序IX而纯合的植株,其甲基化胞嘧啶减少了13%。用甲基化敏感限制酶对这些植株进行DNA凝胶印迹分析,以及对一个180 bp的节结序列进行亚硫酸氢盐测序,结果表明仅在CpNpG位点甲基化减少。在杂合或纯合突变植株的CpG或不对称位点未观察到甲基化减少。我们的研究表明,色域甲基化酶Zmet2是CpNpG序列体内甲基化所必需的。