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The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands

[Image: see text] Targeting of noncanonical DNA structures, such as hairpin loops, may have significant diagnostic and therapeutic potential. Oligonucleotides can be used for binding to mRNA, forming a DNA/RNA hybrid duplex that inhibits translation. This kind of modulation of gene expression is cal...

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Autores principales: Prislan, Iztok, Lee, Hui-Ting, Lee, Cynthia, Marky, Luis A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4291056/
https://www.ncbi.nlm.nih.gov/pubmed/25486129
http://dx.doi.org/10.1021/jp510131c
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author Prislan, Iztok
Lee, Hui-Ting
Lee, Cynthia
Marky, Luis A.
author_facet Prislan, Iztok
Lee, Hui-Ting
Lee, Cynthia
Marky, Luis A.
author_sort Prislan, Iztok
collection PubMed
description [Image: see text] Targeting of noncanonical DNA structures, such as hairpin loops, may have significant diagnostic and therapeutic potential. Oligonucleotides can be used for binding to mRNA, forming a DNA/RNA hybrid duplex that inhibits translation. This kind of modulation of gene expression is called the antisense approach. In order to determine the best strategy to target a common structural motif in mRNA, we have designed a set of stem-loop DNA molecules with sequence: d(GCGCT(n)GTAAT(5)GTTACT(n)GCGC), where n = 1, 3, or 5, “T(5)” is an end loop of five thymines. We used a combination of calorimetric and spectroscopy techniques to determine the thermodynamics for the reaction of a set of hairpins containing internal loops with their respective partially complementary strands. Our aim was to determine if internal- and end-loops are promising regions for targeting with their corresponding complementary strands. Indeed, all targeting reactions were accompanied by negative changes in free energy, indicating that reactions proceed spontaneously. Further investigation showed that these negative free energy terms result from a net balance of unfavorable entropy and favorable enthalpy contributions. In particular, unfolding of hairpins and duplexes is accompanied by positive changes in heat capacity, which may be a result of exposure of hydrophobic groups to the solvent. This study provides a new method for the targeting of mRNA in order to control gene expression.
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spelling pubmed-42910562015-12-08 The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands Prislan, Iztok Lee, Hui-Ting Lee, Cynthia Marky, Luis A. J Phys Chem B [Image: see text] Targeting of noncanonical DNA structures, such as hairpin loops, may have significant diagnostic and therapeutic potential. Oligonucleotides can be used for binding to mRNA, forming a DNA/RNA hybrid duplex that inhibits translation. This kind of modulation of gene expression is called the antisense approach. In order to determine the best strategy to target a common structural motif in mRNA, we have designed a set of stem-loop DNA molecules with sequence: d(GCGCT(n)GTAAT(5)GTTACT(n)GCGC), where n = 1, 3, or 5, “T(5)” is an end loop of five thymines. We used a combination of calorimetric and spectroscopy techniques to determine the thermodynamics for the reaction of a set of hairpins containing internal loops with their respective partially complementary strands. Our aim was to determine if internal- and end-loops are promising regions for targeting with their corresponding complementary strands. Indeed, all targeting reactions were accompanied by negative changes in free energy, indicating that reactions proceed spontaneously. Further investigation showed that these negative free energy terms result from a net balance of unfavorable entropy and favorable enthalpy contributions. In particular, unfolding of hairpins and duplexes is accompanied by positive changes in heat capacity, which may be a result of exposure of hydrophobic groups to the solvent. This study provides a new method for the targeting of mRNA in order to control gene expression. American Chemical Society 2014-12-08 2015-01-08 /pmc/articles/PMC4291056/ /pubmed/25486129 http://dx.doi.org/10.1021/jp510131c Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Prislan, Iztok
Lee, Hui-Ting
Lee, Cynthia
Marky, Luis A.
The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands
title The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands
title_full The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands
title_fullStr The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands
title_full_unstemmed The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands
title_short The Size of the Internal Loop in DNA Hairpins Influences Their Targeting with Partially Complementary Strands
title_sort size of the internal loop in dna hairpins influences their targeting with partially complementary strands
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4291056/
https://www.ncbi.nlm.nih.gov/pubmed/25486129
http://dx.doi.org/10.1021/jp510131c
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