McKibbin R S, Halford N G, Francis D
Department of Agricultural Sciences, University of Bristol, UK.
Plant Mol Biol. 1998 Mar;36(4):601-12. doi: 10.1023/a:1005937011095.
Lateral root formation was examined following the expression of a fission yeast mitotic regulator gene, cdc25, under the control of a tetracycline-inducible promoter in cultured roots of tobacco. Over expression of cdc25 in fission yeast results in premature cell division at a reduced cell size. Our aim was to examine whether cdc25 expression would affect cell size in the tobacco roots, and what effect this would have on lateral root morphogenesis. Transgene integration was confirmed by Southern blotting; it was inherited as a dominant Mendelian trait. Conditions for optimal expression, determined using plants transformed with gus under the control of the same promoter, were: addition of tetracycline (5 micrograms/ml) every 72 h, to cultured roots in Murashige-Skoog liquid medium in darkness at 27 degrees C. After the addition of tetracycline, cdc25 transcripts were detected using RT-PCR, initially after 48 h, and more strongly after 72 h. Appearance of cdc25 transcripts was followed by major changes in the roots. Compared with controls, lateral root primordia were initiated more frequently, were significantly smaller and comprised smaller cells at mitosis. However, cdc25 expression did not perturb normal development of the lateral roots. The data are consistent with cdc25 expression leading to a greater frequency of lateral root primordium formation and establishing a new threshold size for cell division in the primordia which was then maintained throughout subsequent development.
在烟草培养根中,在四环素诱导型启动子的控制下,表达裂殖酵母有丝分裂调节基因cdc25后,对侧根形成进行了检测。cdc25在裂殖酵母中的过表达导致细胞在较小的细胞大小下过早进行细胞分裂。我们的目的是研究cdc25的表达是否会影响烟草根中的细胞大小,以及这会对侧根形态发生产生什么影响。通过Southern印迹法确认了转基因整合;它作为显性孟德尔性状遗传。使用在相同启动子控制下用gus转化的植物确定的最佳表达条件为:在27℃黑暗条件下,在Murashige-Skoog液体培养基中对培养根每72小时添加四环素(5微克/毫升)。添加四环素后,使用RT-PCR检测cdc25转录本,最初在48小时后检测到,72小时后检测到的信号更强。cdc25转录本出现后,根发生了重大变化。与对照相比,侧根原基起始更频繁,明显更小,并且在有丝分裂时包含更小的细胞。然而,cdc25的表达并未干扰侧根的正常发育。这些数据与cdc25的表达导致侧根原基形成频率增加以及为原基中的细胞分裂建立新的阈值大小一致,该阈值大小在随后的整个发育过程中得以维持。