Literature DB >> 3533060

Frequent occurrence of short complementary sequences in nucleic acids.

U Segerstéen, H Nordgren, J C Biro.   

Abstract

The hypothesis, that nucleic acids which code specifically interacting receptor and ligand proteins contain complementary sequences was tested. Human insulin mRNA (HSINSU) contained 16 sequences which were 23.8 +/- 1.4 nucleotides long and were complementary to the insulin receptor mRNA (HSIRPR, 74.8 +/- 1.9% complementary matches, p less than 0.001 compared to randomly occurring matches). However, when examining 10 different nucleic acids (coding proteins not interacting with the insulin receptor), 81 additional sequences were found which were also complementary to HSIRPR. Although the finding of short complementary sequences was statistically highly significant, we concluded that this is not specific for nucleic acids coding specifically interacting proteins.

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Year:  1986        PMID: 3533060     DOI: 10.1016/s0006-291x(86)80084-5

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  4 in total

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2.  Indications that "codon boundaries" are physico-chemically defined and that protein-folding information is contained in the redundant exon bases.

Authors:  Jan Charles Biro
Journal:  Theor Biol Med Model       Date:  2006-08-07       Impact factor: 2.432

3.  The Proteomic Code: a molecular recognition code for proteins.

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Journal:  Theor Biol Med Model       Date:  2007-11-13       Impact factor: 2.432

4.  Discovery of proteomic code with mRNA assisted protein folding.

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  4 in total

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