Benard M, Pierron G
Laboratoire de Biologie et Ultrastructure du Noyau, Institut de Recherches Scientifiques sur le Cancer, Villejuif, France.
Exp Cell Res. 1990 Feb;186(2):299-305. doi: 10.1016/0014-4827(90)90309-x.
Taking advantage of the natural synchrony of the S-phase within the plasmodium of Physarum polycephalum, we extracted highly synchronous DNA samples at precise time points in early S-phase. We then separated, by electrophoresis under denaturating conditions, the newly synthesized DNA strands of the nascent chromosomal replicons from the parental DNA template. Using the cDNA clone of the early-replicating LAV1-2 gene as a probe, we could establish by filter hybridization that the elongation rate of the replicon which encompasses this gene is constant, at a rate of 1 kb/min during the first 30 min of S-phase. The smallest replication intermediate (RI) that we have detected by probing with the LAV1-2 cDNA was 5 kb long, suggesting that the LAV1-2 gene and its origin of replication are closely associated within the chromosome. This procedure should facilitate the mapping of replication origins within the genome of Physarum.
利用多头绒泡菌原质团中S期的自然同步性,我们在S期早期的精确时间点提取了高度同步的DNA样本。然后,在变性条件下通过电泳,将新生染色体复制子新合成的DNA链与亲本DNA模板分离。使用早期复制的LAV1-2基因的cDNA克隆作为探针,我们通过滤膜杂交确定,包含该基因的复制子在S期的前30分钟内,延伸速率恒定,为1 kb/分钟。我们用LAV1-2 cDNA探针检测到的最小复制中间体(RI)长5 kb,这表明LAV1-2基因及其复制起点在染色体内紧密相连。该方法应有助于绘制多头绒泡菌基因组内的复制起点图谱。