Wilson R, Chiang K S
J Cell Biol. 1977 Feb;72(2):470-81. doi: 10.1083/jcb.72.2.470.
Approximately 90% of the Chlamydomonas reinhardtii chloroplast and cytoplasmic rRNAs was transcribed in the nuclear G1 phase, which occurred during the light period under an alternating light-dark synchronization regime of 12 h each. The remaining 10% of chloroplast and cytoplasmic rRNAs was transcribed from its respective DNAs in the dark period, in the midst of an apparent turnover of a transcription appeared to be prokaryotic in sophistication. The transcription was not interrupted during chloroplast DNA synthesis which occurred during the light period. However, transcription of the nuclear DNA was repressed severely during the nuclear S phase in the dark period. The patterns of incorporation of 32P into chloroplast and cytoplasmic rRNA species in the cell cycle were similar to those of the actual rRNA synthesis as measured optically. However, the quantity of 32P incorporation per unit amount of rRNA synthesized varied considerably during the cell cycle, increasing in all rRNA's during the dark period. 32P incorporation data obtained from continuous and pulse 32P-labeling experiments also revealed a turnover of a small amount of both cytoplasmic and chloroplast rRNAs at the end of the S phase. The 32P incorporation into cytoplasmic and chloroplast rRNAs was well matched temporally with the 32P incorporation into their corresponding ribosomes, indicating that the newly synthesized rRNA molecules are utilized without delay throughout the cell cycle in the assembly of ribosomes.
约90%的莱茵衣藻叶绿体和细胞质rRNA是在核G1期转录的,此时期发生在12小时光照和12小时黑暗交替同步培养条件下的光照阶段。其余10%的叶绿体和细胞质rRNA是在黑暗阶段从各自的DNA转录而来,此时转录过程似乎正处于一种明显的周转状态,其复杂性类似于原核生物。在光照阶段发生叶绿体DNA合成期间,转录并未中断。然而,在黑暗阶段的核S期,核DNA的转录受到严重抑制。细胞周期中32P掺入叶绿体和细胞质rRNA种类的模式与通过光学测量的实际rRNA合成模式相似。然而,在细胞周期中,每合成单位量rRNA的32P掺入量变化很大,在黑暗阶段所有rRNA的掺入量都增加。从连续和脉冲32P标记实验获得的32P掺入数据还显示,在S期末期,少量细胞质和叶绿体rRNA存在周转。32P掺入细胞质和叶绿体rRNA的情况在时间上与32P掺入其相应核糖体的情况非常匹配,这表明新合成的rRNA分子在整个细胞周期中都能立即用于核糖体的组装。