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From oligonucleotide shapes to genomic SELEX novel biological regulatory loops


From oligonucleotide shapes to genomic SELEX: novel biological regulatory loops.

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The SELEX method and oligonucleotide combinatorial chemistry discovery process yields high-affinity/high-specificity ligands for virtually any molecular target. Typically, the enormous starting libraries used in the SELEX process contain 10(14)-10(15) sequences. We now ask if the smaller sequences, complexity of extant organisms, and evolutionary history provide useful interactions between oligonucleotides and at least some unexpected targets. That is, do organisms contain a robust linkage map between their oligonucleotides and proteins and/or small molecules that enriches life?


Gold L, Brown D, He Y, Shtatland T, Singer BS, Wu Y

Proceedings of the National Academy of Sciences of the United States of America

1997-01-07 00:00

94

1

59-64

Base Sequence,Binding Sites,DNA-Directed DNA Polymerase,Evolution, Molecular,Gene Expression Regulation,Ligands,Molecular Biology,Molecular Sequence Data,Nucleic Acid Conformation,Oligoribonucleotides,RNA,Viral Proteins,Ligands,Oligoribonucleotides,Viral Proteins,gene 43 protein, Enterobacteria phage T4,RNA,DNA-Directed DNA Polymerase

University of Colorado at Boulder, Department of Molecular, Cellular, and Developmental Biology, 80309-0347, USA

Proc. Natl. Acad. Sci. U.S.A.


0027-8424




402

True

8990161

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