Kessel M, Rosenberger R F
J Bacteriol. 1968 Jun;95(6):2275-81. doi: 10.1128/jb.95.6.2275-2281.1968.
Pulse labeling of deoxyribonucleic acid (DNA) and radioautography have been used to study the effect of growth rate on nuclear replication in Aspergillus nidulans. When conidia were germinated in media supporting a fast growth rate, the radioactive pulse labeled either all of the nuclei in a cell or none of them. At slower growth rates, hyphae contained both labeled and unlabeled nuclei. Altering the growth rate thus changed nuclear replication from simultaneous to sequential. The time taken to duplicate the DNA in a nucleus, estimated from the ratio of labeled to total nuclei, remained constant at the different doubling times. The distribution of label showed that nuclei in the same hypha spent unequal times in both the postmitotic gap (G1) and the premitotic gap (G2) periods when grown at slow rates. These unequal G1 and G2 periods are considered to cause asynchrony. Once DNA synthesis was out of phase through growth on a poor medium, transferring the hypha to a rich medium did not resynchronize the nuclei. To interpret the data, two initiator mechanisms, one starting DNA synthesis and the other mitosis, are postulated to control nuclear replication in A. nidulans.
利用脱氧核糖核酸(DNA)的脉冲标记和放射自显影技术,研究了生长速率对构巢曲霉细胞核复制的影响。当分生孢子在支持快速生长速率的培养基中萌发时,放射性脉冲要么标记细胞中的所有细胞核,要么不标记任何细胞核。在较慢的生长速率下,菌丝中既有标记的细胞核,也有未标记的细胞核。因此,改变生长速率会使细胞核复制从同步变为顺序进行。根据标记细胞核与总细胞核的比例估算,细胞核复制DNA所需的时间在不同的倍增时间下保持恒定。标记分布表明,在缓慢生长时,同一菌丝中的细胞核在有丝分裂后间隙(G1)和有丝分裂前间隙(G2)期所花费的时间不相等。这些不相等的G1和G2期被认为会导致不同步。一旦通过在贫瘠培养基上生长使DNA合成不同步,将菌丝转移到丰富培养基中并不能使细胞核重新同步。为了解释这些数据,假定了两种起始机制,一种启动DNA合成,另一种启动有丝分裂,以控制构巢曲霉的细胞核复制。