Maden B E, Reeder R H
Nucleic Acids Res. 1979 Mar;6(3):817-30. doi: 10.1093/nar/6.3.817.
Xenopus laevis rRNA was hybridised to either of two cloned fragments of ribosomal DNA. One fragment, designated X1r11, contains a short region of the 18 S rRNA gene and most of the 28 S rRNA gene. The other fragment, X1r14, contains a short region of the 28 S gene and most of the 18 S gene. After hybridization the non-complementary rRNA was removed by digestion with T1 RNase and the hybridized RNA was then eluted and examined by fingerprinting analysis. The 3' terminal sequence and the dimethyl-A-containing sequence of 18 S rRNA both hybridized to X1r11 rDNA, in agreement with the known direction of transcription of rDNA. The distribution of other methylated oligonucleotides between the various fingerprints permitted assigment of nearly all of the methylated sequences in 18 S and 28 s rRNA to either the short 3' region or the long 5' region of the respective molecules.
非洲爪蟾的rRNA与核糖体DNA的两个克隆片段之一进行杂交。一个片段,命名为X1r11,包含18 S rRNA基因的一个短区域和大部分28 S rRNA基因。另一个片段X1r14,包含28 S基因的一个短区域和大部分18 S基因。杂交后,用T1核糖核酸酶消化去除非互补的rRNA,然后洗脱杂交的RNA,并通过指纹分析进行检测。18 S rRNA的3'末端序列和含二甲基-A的序列都与X1r11 rDNA杂交,这与rDNA已知的转录方向一致。各种指纹图谱中其他甲基化寡核苷酸的分布使得几乎所有18 S和28 S rRNA中的甲基化序列都可归属于相应分子的短3'区域或长5'区域。