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The use of nuclease P1in sequence analysis of end group labeled RNA

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Silberklang, M., Gillum, A.M., Rajbhandary, U.L.·1977·Nucleic Acids Research

Abstract

A method is described for the direct sequence analysis of 20-25 nucleotides from the termini of 5'- or 3'-end-group [32P] labeled RNA. The method involves partial endonucleolytic digestion of the labeled RNA with nuclease P1 (from Penicillium citrinum) followed by separation of the partial digestion products by two-dimensional homochromatography, the nucleotide sequence being determined by mobility shift analysis. This procedure has been applied to the sequence analysis of the terminal regions of tRNAs and of high molecular weight RNA, such as messenger RNA or viral RNA. A further application involves its use in conjunction with snake venom phosphodiesterase to determine the sequence of 5'-end group labeled oligonucleotides, containing modified bases, derived from T1 or pancreatic RNase digestion of tRNA.

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Metadata

Authors
Silberklang, M., Gillum, A. M., & Rajbhandary, U. L.
Venue
Nucleic Acids Research
Published
1977
Volume
4
Issue
12
Pages
4091-4108
ISSN
  • 0305-1048 (ISSN-L)
  • 1362-4962
OpenAlex
W2040179169
Cited by
238
References
0
FWCI
8.99
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: The use of nuclease P1in sequence analysis of end group labeled RNA. https://app.cochat.ai/papers/10.1093/nar/4.12.4091
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Silberklang, M., Gillum, A. M., & Rajbhandary, U. L. (1977). The use of nuclease P1in sequence analysis of end group labeled RNA. Nucleic Acids Research. https://doi.org/10.1093/nar/4.12.4091

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