Nikaido S S, Locke C R, Weeks D P
Department of Biochemistry, University of Nebraska-Lincoln 68583-0718.
Plant Mol Biol. 1994 Oct;26(1):275-84. doi: 10.1007/BF00039538.
The development of techniques allowing the unattended collection of RNA from cell samples at room temperature makes practical accurate and facile monitoring of circadian rhythms in Chlamydomonas reinhardtii. The utility of these methods was demonstrated by collecting RNA samples for three days from cells maintained in continuous darkness. Every hour, cells were automatically collected and lysed with buffer containing SDS and proteinase K. Samples were maintained at room temperature with little or no evidence of degradation of RNA. Strong, non-damping circadian rhythms of cab mRNA abundance were measured. Free-running rhythms of about 24 h were measured from cultures maintained at 16, 20, 25 and 30 degrees C, thus demonstrating temperature compensation of circadian period. Simultaneous collections from cultures previously entrained to 12 h light/12 h dark cycles of opposite phase displayed circadian rhythms of cab mRNA abundance that were in phase with their previous entraining light cycles. Thus, this result suggests that the measured circadian rhythms of cab mRNA abundance was not an artifact of the collection procedure.
能够在室温下无人值守地从细胞样本中收集RNA的技术发展,使得对莱茵衣藻昼夜节律进行准确且便捷的监测成为可能。通过从处于持续黑暗环境中的细胞收集三天的RNA样本,证明了这些方法的实用性。每小时自动收集细胞,并用含有SDS和蛋白酶K的缓冲液裂解。样本在室温下保存,几乎没有或没有RNA降解的迹象。测量到了cab mRNA丰度强烈的、无衰减的昼夜节律。从在16、20、25和30摄氏度下培养的培养物中测量到约24小时的自由运转节律,从而证明了昼夜周期的温度补偿。同时从先前被训练为相反相位的12小时光照/12小时黑暗周期的培养物中收集样本,显示出cab mRNA丰度的昼夜节律与它们先前的训练光照周期同步。因此,这一结果表明,所测量的cab mRNA丰度的昼夜节律不是收集过程的人为产物。