Dhar S K, Choudhury N R, Mittal V, Bhattacharya A, Bhattacharya S
Genetic Engineering Unit, Jawaharlal Nehru University, New Delhi, India.
Mol Cell Biol. 1996 May;16(5):2314-24. doi: 10.1128/MCB.16.5.2314.
In the protozoan parasite Entamoeba histolytica (which causes amoebiasis in humans), the rRNA genes (rDNA) in the nucleus are carried on an extrachromosomal circular plasmid. For strain HM-1:IMSS, the size of the rDNA plasmid is 24.5 kb, and 200 copies per genome are present. Each circle contains two rRNA transcription units as inverted repeats separated by upstream and downstream spacers. We have studied the replication of this molecule by neutral/neutral two-dimensional gel electrophoresis and by electron microscopy. All restriction fragments analyzed by two-dimensional gel electrophoresis gave signals corresponding to simple Y's and bubbles. This showed that replication initiated in this plasmid at multiple, dispersed locations spread throughout the plasmid. On the basis of the intensity of the bubble arcs, initiations from the rRNA transcription units seemed to occur more frequently than those from intergenic spacers. Multiple, dispersed initiation sites were also seen in the rDNA plasmid of strain HK-9 when it was analyzed by two-dimensional gel electrophoresis. Electron microscopic visualization of replicating plasmid molecules in strain HM-1:IMISS showed multiple replication bubbles in the same molecule. The location of bubbles on the rDNA circle was mapped by digesting with PvuI or BsaHI, which linearize the molecule, and with SacII, which cuts the circle twice. The distance of the bubbles from one end of the molecule was measured by electron microscopy. The data corroborated those from two-dimensional gels and showed that replication bubbles were distributed throughout the molecule and that they appeared more frequently in rRNA transcription units. The same interpretation was drawn from electron microscopic analysis of the HK-9 plasmid. Direct demonstration of more than one bubble in the same molecule is clear evidence that replication of this plasmid initiates at multiple sites. Potential replication origins are distributed throughout the plasmid. Such a mechanism is not known to operate in any naturally occurring prokaryotic or eukaryotic plasmid.
在原生动物寄生虫溶组织内阿米巴(可导致人类患阿米巴病)中,细胞核中的核糖体RNA基因(rDNA)位于一个染色体外环状质粒上。对于HM-1:IMSS菌株,rDNA质粒大小为24.5 kb,每个基因组中有200个拷贝。每个环包含两个作为反向重复序列的rRNA转录单元,由上游和下游间隔区隔开。我们通过中性/中性二维凝胶电泳和电子显微镜研究了该分子的复制。通过二维凝胶电泳分析的所有限制性片段都给出了对应于简单Y形和泡状结构的信号。这表明该质粒的复制在多个分散的位置起始,遍布整个质粒。根据泡状弧的强度,rRNA转录单元起始的频率似乎比基因间隔区更高。当通过二维凝胶电泳分析时,在HK-9菌株的rDNA质粒中也观察到多个分散的起始位点。对HM-1:IMISS菌株中复制质粒分子的电子显微镜观察显示同一分子中有多个复制泡。通过用使分子线性化的PvuI或BsaHI以及切割环两次的SacII进行消化,确定了rDNA环上泡状结构的位置。通过电子显微镜测量泡状结构距分子一端的距离。数据证实了二维凝胶电泳的结果,表明复制泡分布在整个分子中,并且在rRNA转录单元中出现得更频繁。对HK-9质粒的电子显微镜分析也得出了相同的结论。同一分子中存在多个泡的直接证据清楚地表明该质粒的复制在多个位点起始。潜在的复制起点分布在整个质粒中。这种机制在任何天然存在的原核或真核质粒中都未发现。