Characterisation of RNA Fragments Obtained by Mild Nuclease Digestion of 30‐S Ribosomal Subunits from Escherichia coli

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Abstract
When Escherichia coli 30‐S ribosomal subunits are hydrolysed under mild conditions, two ribonucleoprotein fragments of unequal size are produced. Knowledge of the RNA sequences contained in these hydrolysis products was required for the experiments described in the preceding paper, and the RNA sub‐fragments have therefore been examined by oligonucleotide analysis. Two well‐defined small fragments of free RNA, produced concomitantly with the ribonucleoprotein fragments, were also analysed. The larger ribonucleoprotein fragment, containing predominantly proteins S4, S5, S8, S15, S16 (17) and S20, contains a complex mixture of RNA sub‐fragments varying from about 100 to 800 nucleotides in length. All these fragments arose from the 5′‐terminal 900 nucleotides of 16‐S RNA, corresponding to the well‐known 12‐S fragment. No long‐range interactions could be detected within this RNA region in these experiments. The RNA from the smaller ribonucleoprotein fragment (containing proteins S7, S9, S10, S14 and S19) has been described in detail previously, and consists of about 450 nucleotides near the 3′ end of the 16‐S RNA, but lacking the 3′‐terminal 150 nucleotides. The two small free RNA fragments (above) partly account for these missing 150 nucleotides; both fragments arose from section A of the 16‐S RNA, but section J (the 3′‐terminal 50 nucleotides) was not found. This result suggests that the 3′ region of 16‐S RNA is not involved in stable interactions with protein.