Klöti A, He X, Potrykus I, Hohn T, Fütterer J
Institute of Plant Sciences, Federal Institute of Technology, Universitätstrasse 2, CH 8092 Zürich, Switzerland.
Proc Natl Acad Sci U S A. 2002 Aug 6;99(16):10881-6. doi: 10.1073/pnas.152330299. Epub 2002 Jul 19.
In a transgenic rice line, a beta-glucuronidase reporter gene under the control of the rice tungro bacilliform virus promoter became gradually methylated, and gene activity was lost concomitantly. Methylation was observed only in the homozygous offspring and was initially restricted to the promoter region and accompanied by loss of expression in the vascular bundle tissue only. This expression pattern was similar to that of a promoter with a deletion of a vascular bundle expression element. The gene activity could be reestablished by treatment with 5-azacytidine. Methylation per se did not inhibit the binding to the promoter region of protein factors which also bound to the unmethylated sequence. Instead, promoter methylation enabled the alternative binding of a protein with specificity for sequence and methylation. In further generations of homozygous offspring the methylation spread into the transcribed region and gene activity was completely repressed also in nonvascular cells. The results indicate that different stages are involved in DNA methylation-correlated gene inactivation, and that at least one of them may involve the attraction of a sequence and methylation-specific DNA-binding protein.
在一个转基因水稻品系中,受水稻东格鲁杆状病毒启动子控制的β-葡萄糖醛酸酶报告基因逐渐发生甲基化,同时基因活性丧失。甲基化仅在纯合子后代中观察到,最初局限于启动子区域,且仅伴随着维管束组织中表达的丧失。这种表达模式类似于缺失维管束表达元件的启动子的表达模式。用5-氮杂胞苷处理可重新建立基因活性。甲基化本身并不抑制与未甲基化序列结合的蛋白质因子与启动子区域的结合。相反,启动子甲基化使得一种对序列和甲基化具有特异性的蛋白质能够进行选择性结合。在纯合子后代的进一步世代中,甲基化扩散到转录区域,并且在非维管细胞中基因活性也被完全抑制。结果表明,DNA甲基化相关的基因失活涉及不同阶段,并且其中至少一个阶段可能涉及序列和甲基化特异性DNA结合蛋白的吸引。