Fedoroff N, Schläppi M, Raina R
Carnegie Institution of Washington, Department of Embryology, Baltimore, Maryland 21210, USA.
Bioessays. 1995 Apr;17(4):291-7. doi: 10.1002/bies.950170405.
Expression and transposition of the Suppressor-mutator (Spm) transposon of maize are controlled by interacting epigenetic and autoregulatory mechanisms. Methylation of critical element sequences prevents both transcription and transposition, heritably inactivating the element. The promoter, comprising the terminal 0.2 kb of the element, and a 0.35-kb, highly GC-rich, downstream sequence are the methylation target sequences. The element encodes two proteins necessary for transposition, TnpA and TnpD. There are multiple TnpA binding sites, both in the 5' terminal promoter region and at the element's 3' end. In addition to its role in transposition, TnpA is both a positive and a negative regulator of transcription. TnpA represses the element's promoter when it is not methylated. When the element is inactive and its promoter methylated, TnpA activates the methylated promoter and facilitates both its transient and heritable demethylation.
玉米抑制突变体(Spm)转座子的表达和转座受表观遗传和自动调节机制的相互作用控制。关键元件序列的甲基化会阻止转录和转座,使元件遗传性失活。启动子由元件末端0.2 kb组成,以及一个0.35 kb、高度富含GC的下游序列是甲基化靶序列。该元件编码转座所需的两种蛋白质,TnpA和TnpD。在5'末端启动子区域和元件的3'末端都有多个TnpA结合位点。除了在转座中的作用外,TnpA还是转录的正调节因子和负调节因子。当元件未甲基化时,TnpA会抑制其启动子。当元件失活且其启动子甲基化时,TnpA会激活甲基化启动子,并促进其瞬时和遗传性去甲基化。