Braga E A, Yussifov T N, Nosikov V V
Gene. 1982 Dec;20(2):145-56. doi: 10.1016/0378-1119(82)90033-6.
Structural organization of the rat ribosomal repeating unit was studied using hybridization of blotted restriction fragments of total rat DNA with alpha-32P-labeled cDNA probe synthesized on the 18S and 28S rRNAs. A detailed restriction endonuclease map was constructed, the 18S and 28S rRNA genes mapped and the sizes of the rat ribosomal repeating units determined. Considerable site heterogeneity of rat rDNA was revealed in both nontranscribed and external transcribed spacers. Recombinant phages containing the whole set of transcribed regions and a considerable part of a nontranscribed spacer of the rDNA were selected from the rat gene library. The restriction maps of the cloned rDNA fragments are in good agreement with the map constructed by Southern's technique, add to this map and support the existence of site heterogeneity in ribosomal repeating units. Proximal to the 3'-end of the 28S rRNA gene an internally repetitive region was found, each repeating unit being equal to approx. 150 bp. The site for transcription initiation was mapped 4.0-4.5 kb upstream from the 5'-end of the 18S rRNA gene. Frequently reiterated interspersed sequences were found in the nontranscribed spacer at approx. 2-3 kb distance from both ends of the transcribed region.
利用大鼠总DNA经酶切后的片段与以18S和28S rRNA为模板合成的α-32P标记的cDNA探针杂交,研究了大鼠核糖体重复单位的结构组织。构建了详细的限制性内切酶图谱,对18S和28S rRNA基因进行了定位,并确定了大鼠核糖体重复单位的大小。在非转录间隔区和外部转录间隔区均发现大鼠rDNA存在显著的位点异质性。从大鼠基因文库中筛选出含有rDNA全套转录区和相当一部分非转录间隔区的重组噬菌体。克隆的rDNA片段的限制性图谱与用Southern技术构建的图谱高度吻合,补充了该图谱,并支持核糖体重复单位中存在位点异质性。在28S rRNA基因的3′端附近发现了一个内部重复区域,每个重复单位约为150 bp。转录起始位点定位于18S rRNA基因5′端上游4.0 - 4.5 kb处。在距转录区两端约2 - 3 kb的非转录间隔区发现了频繁重复的散布序列。