Quélo A-H, Verbelen J-P
Department of Biology, Universitaire Instelling Antwerpen, Universiteitsplein 1, 2610 Wilrijk, Belgium.
Protoplasma. 2004 Jun;223(2-4):197-202. doi: 10.1007/s00709-004-0043-9. Epub 2004 Jun 22.
Newly synthesized DNA can be observed on chromosomes or extended chromatin fibers after incorporation and immunodetection of bromodeoxyuridine. This technique, frequently used in animal cells, was adapted for use in BY-2 cells. For the first time, the origins of replication in plant cells could be visualized and monitored on DNA fibers without the use of radioactive traces. The replicon size for BY-2 cells was estimated to be 12.9 microm; and the fork rate, 1.17 microm/h. These values are comparable to those reported for tomato and mustard cells. Furthermore, the data confirm our previous observation that DNA synthesis is not totally blocked by aphidicolin. Bromodeoxyuridine incorporation into DNA was obvious from 24 h onwards after treatment with aphidicolin.
在掺入溴脱氧尿苷并进行免疫检测后,可在染色体或伸展的染色质纤维上观察到新合成的DNA。这种技术常用于动物细胞,现被应用于BY-2细胞。首次能够在不使用放射性示踪剂的情况下,在DNA纤维上可视化并监测植物细胞中的复制起点。BY-2细胞的复制子大小估计为12.9微米;叉速率为1.17微米/小时。这些值与报道的番茄和芥菜细胞的值相当。此外,数据证实了我们之前的观察结果,即放线菌素并不能完全阻断DNA合成。在用放线菌素处理后24小时起,溴脱氧尿苷掺入DNA的情况就很明显。