Deoxyribozymes that recode sequence information.

Abstract:

:Allosteric nucleic acid ligases have been used previously to transform analyte-binding into the formation of oligonucleotide templates that can be amplified and detected. We have engineered binary deoxyribozyme ligases whose two components are brought together by bridging oligonucleotide effectors. The engineered ligases can 'read' one sequence and then 'write' (by ligation) a separate, distinct sequence, which can in turn be uniquely amplified. The binary deoxyribozymes show great specificity, can discriminate against a small number of mutations in the effector, and can read and recode DNA information with high fidelity even in the presence of excess obscuring genomic DNA. In addition, the binary deoxyribozymes can read non-natural nucleotides and write natural sequence information. The binary deoxyribozyme ligases could potentially be used in a variety of applications, including the detection of single nucleotide polymorphisms in genomic DNA or the identification of short nucleic acids such as microRNAs.

journal_name

Nucleic Acids Res

journal_title

Nucleic acids research

authors

Tabor JJ,Levy M,Ellington AD

doi

10.1093/nar/gkl176

subject

Has Abstract

pub_date

2006-04-28 00:00:00

pages

2166-72

issue

8

eissn

0305-1048

issn

1362-4962

pii

34/8/2166

journal_volume

34

pub_type

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