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Method to determine the reading frame of a protein from the purine/pyrimidine genome sequence and its possible evolutionary justification.

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Shepherd, J C·1981·Proceedings of the National Academy of Sciences

Abstract

The periodic variations obtained by correlating the relative positions of purines and pyrimidines (and of the four bases thymine, cytosine, adenine, and guanine) in a wide variety of genomes of wholly or partly known sequence suggest that there may be enough of an earlier comma-free coding system (i.e., only readable in one frame) still present to permit determination of the reading frame and approximate extent of the present protein coding stretches. The characteristics of these variations support the hypothesis that these primitive messages were formed of coding triplets having the form RNY (R = purine; Y = pyrimidine; and N = purine or pyrimidine). The base sequences and reading frames that have a minimal deviation from such a message are still good predictors of actual coding regions and reading frames in spite of the many mutations that have occurred since such a genetic code was last in use. In fact, the right frame for almost all the proteins in a number of viruses and various prokaryotes and eukaryotes is deduced purely from purine/pyrimidine information and not by using the normal start and stop signals.

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Metadata

Authors
Shepherd, J. C.
Venue
Proceedings of the National Academy of Sciences
Published
1981-03
Volume
78
Issue
3
Pages
1596-1600
ISSN
  • 0027-8424 (ISSN-L)
  • 1091-6490
OpenAlex
W2088549477
Cited by
316
References
0
FWCI
5.25
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: Method to determine the reading frame of a protein from the purine/pyrimidine genome sequence and its possible evolutionary justification. https://app.cochat.ai/papers/10.1073/pnas.78.3.1596
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Shepherd, J. C. (1981). Method to determine the reading frame of a protein from the purine/pyrimidine genome sequence and its possible evolutionary justification. Proceedings of the National Academy of Sciences. https://doi.org/10.1073/pnas.78.3.1596

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