Huber M, Koller B, Gitler C, Mirelman D, Revel M, Rozenblatt S, Garfinkel L
Weizmann Institute of Science, Department of Biophysics, Rehovot, Israel.
Mol Biochem Parasitol. 1989 Jan 15;32(2-3):285-96. doi: 10.1016/0166-6851(89)90077-7.
Highly abundant DNA fragments obtained after restriction enzyme digests of nuclear DNA of Entamoeba histolytica strain HM-1:IMSS have been cloned and characterized. Northern blot hybridization to E. histolytica rRNA and sequence analysis identified the abundant DNAs as ribosomal DNA containing species. Several overlapping clones containing these abundant DNAs were isolated from 4 different genomic libraries of E. histolytica. Alignment of the restriction maps was consistent with a circular molecule, about 24.6 kilobase pairs (kb) in size. Nuclease BA131 digestion provided additional evidence for the circular nature of this DNA. The ribosomal DNA molecule contains two large inverted repeat-regions, each at least 5.2 kb in length. Sequence analysis of clone R715 revealed homology to the large rRNA units of various eukaryotic organisms. This clone was located in both inverted repeats, suggesting two rRNA cistrons per molecule. The inverted repeats are flanked by stretches of DNA which contain tandemly reiterated sequences. Southern blot analysis of E. histolytica nuclear DNA revealed the presence of two populations of molecules. These molecules have identical arrangements of restriction sites, but differ in size (0.7 kb) in a fragment containing tandemly reiterated sequences. Analysis of E. histolytica nuclear DNA by electron microscopy also revealed circular molecules. These molecules are about 26.6 kb +/- 0.5 kb in size and contain structural features predicted by the restriction map of the extrachromosomal ribosomal DNA of E. histolytica.
对溶组织内阿米巴菌株HM-1:IMSS的核DNA进行限制性内切酶消化后获得的高度丰富的DNA片段已被克隆和鉴定。与溶组织内阿米巴rRNA的Northern印迹杂交和序列分析确定这些丰富的DNA为含核糖体DNA的物种。从溶组织内阿米巴的4个不同基因组文库中分离出了几个包含这些丰富DNA的重叠克隆。限制性图谱的比对与一个大小约为24.6千碱基对(kb)的环状分子一致。核酸酶BA131消化为该DNA的环状性质提供了额外证据。核糖体DNA分子包含两个大的反向重复区域,每个区域长度至少为5.2 kb。克隆R715的序列分析显示与各种真核生物的大rRNA单位具有同源性。该克隆位于两个反向重复序列中,表明每个分子有两个rRNA顺反子。反向重复序列两侧是含有串联重复序列的DNA片段。对溶组织内阿米巴核DNA的Southern印迹分析显示存在两种分子群体。这些分子具有相同的限制性酶切位点排列,但在一个包含串联重复序列的片段中大小不同(相差0.7 kb)。通过电子显微镜对溶组织内阿米巴核DNA的分析也显示出环状分子。这些分子大小约为26.6 kb +/- 0.5 kb,并且包含由溶组织内阿米巴染色体外核糖体DNA的限制性图谱预测的结构特征。