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Processing in the 5′ region of the pnp transcript facilitates the site-specific endonucleolytic cleavages of mRNA
Author(s) -
Renkichi Takata,
Mika Izuhara,
Koichi Akiyama
Publication year - 1992
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/20.4.847
Subject(s) - biology , polynucleotide phosphorylase , rnase p , cleavage (geology) , messenger rna , gene , microbiology and biotechnology , primary transcript , ribonuclease iii , rnase h , ribonuclease , escherichia coli , genetics , rna , enzyme , biochemistry , purine nucleoside phosphorylase , rna interference , alternative splicing , paleontology , purine , fracture (geology)
The primary transcript of pnp, the gene encoding polynucleotide phosphorylase in Escherichia coli, is processed in the 5' end region by ribonuclease III (RNase III). The unprocessed transcript shows enhanced stability compared with the processed transcript. We report here that, unlike the processed transcript, the unprocessed pnp transcript did not accept endonucleolytic attack at, at least, five cleavage sites. Sequencing analysis of the four cleavage products shows no sequence specific to all these sites, but AU rich stretches were observed at three sites.

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