Abstract
Two modifications in the Sanger two dimensional electrophoretic procedure for RNA analysis are reported. One increases resolution on the primary fingerprint to the point that digests of large RNAs, of the size 1500-3000 nucleotides yield well resolved fingerprint patterns. The other is a novel endonucleolytic procedure that proves useful in determining sequences of the large oligonucleotides produced by T1 ribonuclease. These modifications have been used in determining the catalogs of oligomers produced by T1 ribonuclease digestion of 16S rRNAs from three related organisms, Bacillus subtilis, B.pumilus and B.stearothermophilus. The possible effects of adaptation to a thermophilic niche on ribosomal RNA primary structure and the phylogenetic relatedness of the two mesophilic Bacilli are discussed.
MeSH Terms
Animals
Bacillus
Bacillus subtilis
Base Sequence
Biological Evolution
Dogs
Geobacillus stearothermophilus
Humans
Infant, Newborn
Phylogeny
RNA, Bacterial/analysis
RNA, Ribosomal/analysis
Species Specificity
Chemicals
RNA, Bacterial
RNA, Ribosomal
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Woese C
Sogin M
Stahl D
Lewis B J
Bonen L
References (13)
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