Lohmann K, Kraus K
Nucleic Acids Res. 1985 Jul 25;13(14):5145-55. doi: 10.1093/nar/13.14.5145.
We have analysed the Eco RI restriction pattern of rDNA of the newt Triturus vulgaris and of some other amphibian species by Southern blotting and hybridization with nick-translated Xenopus rDNA prepared from the recombinant plasmids pXlr11 and pXlr12 (21). After hybridization with r11, the 28S coding fragments become visible in two bands, a prominent one of 5.3 kb and a weak band of 5.9 kb representing about 8% of the 28S genes. The evidence obtained so far by additional digestions with Bam HI and Bgl II indicates that in this species and in Triturus helveticus the coding regions of the 5.9 kb fragments are interrupted by an insertion 0.6 kb in length located in a 1.6 kb Bgl II fragment at the 3' end of the Eco RI fragment, which we believe to be the first described in a vertebrate.
我们通过Southern印迹法,并与从重组质粒pXlr11和pXlr12制备的缺口平移非洲爪蟾rDNA杂交,分析了普通蝾螈及其他一些两栖动物物种的rDNA的Eco RI限制性酶切图谱(21)。用r11杂交后,28S编码片段在两条带中可见,一条突出的5.3 kb带和一条弱的5.9 kb带,后者约占28S基因的8%。到目前为止,通过用Bam HI和Bgl II进行额外酶切获得的证据表明,在该物种和瑞士蝾螈中,5.9 kb片段的编码区被一个长度为0.6 kb的插入片段打断,该插入片段位于Eco RI片段3'端的一个1.6 kb Bgl II片段中,我们认为这是在脊椎动物中首次描述的。