The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure

Stretches of cytosine-rich DNA are capable of adopting a dynamic secondary structure, the i-motif. When within promoter regions, the i-motif has the potential to act as a molecular switch for controlling gene expression. However, i-motif structures in genomic areas of repetitive nucleotide sequences...

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Main Authors: Susie L. Brown, Samantha Kendrick
Format: Article
Language:English
Published: MDPI AG 2021-01-01
Series:Pharmaceuticals
Subjects:
Online Access:https://www.mdpi.com/1424-8247/14/2/96
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spelling doaj-024f86d45e184cf18b33c0f006865d552021-01-28T00:01:44ZengMDPI AGPharmaceuticals1424-82472021-01-0114969610.3390/ph14020096The i-Motif as a Molecular Target: More than a Complementary DNA Secondary StructureSusie L. Brown0Samantha Kendrick1Biochemistry and Molecular Biology Department, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USABiochemistry and Molecular Biology Department, University of Arkansas for Medical Sciences, Little Rock, AR 72205, USAStretches of cytosine-rich DNA are capable of adopting a dynamic secondary structure, the i-motif. When within promoter regions, the i-motif has the potential to act as a molecular switch for controlling gene expression. However, i-motif structures in genomic areas of repetitive nucleotide sequences may play a role in facilitating or hindering expansion of these DNA elements. Despite research on the i-motif trailing behind the complementary G-quadruplex structure, recent discoveries including the identification of a specific i-motif antibody are pushing this field forward. This perspective reviews initial and current work characterizing the i-motif and providing insight into the biological function of this DNA structure, with a focus on how the i-motif can serve as a molecular target for developing new therapeutic approaches to modulate gene expression and extension of repetitive DNA.https://www.mdpi.com/1424-8247/14/2/96i-motifDNA quadruplex structurestranscription regulationcancer therapeutics
collection DOAJ
language English
format Article
sources DOAJ
author Susie L. Brown
Samantha Kendrick
spellingShingle Susie L. Brown
Samantha Kendrick
The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure
Pharmaceuticals
i-motif
DNA quadruplex structures
transcription regulation
cancer therapeutics
author_facet Susie L. Brown
Samantha Kendrick
author_sort Susie L. Brown
title The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure
title_short The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure
title_full The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure
title_fullStr The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure
title_full_unstemmed The i-Motif as a Molecular Target: More than a Complementary DNA Secondary Structure
title_sort i-motif as a molecular target: more than a complementary dna secondary structure
publisher MDPI AG
series Pharmaceuticals
issn 1424-8247
publishDate 2021-01-01
description Stretches of cytosine-rich DNA are capable of adopting a dynamic secondary structure, the i-motif. When within promoter regions, the i-motif has the potential to act as a molecular switch for controlling gene expression. However, i-motif structures in genomic areas of repetitive nucleotide sequences may play a role in facilitating or hindering expansion of these DNA elements. Despite research on the i-motif trailing behind the complementary G-quadruplex structure, recent discoveries including the identification of a specific i-motif antibody are pushing this field forward. This perspective reviews initial and current work characterizing the i-motif and providing insight into the biological function of this DNA structure, with a focus on how the i-motif can serve as a molecular target for developing new therapeutic approaches to modulate gene expression and extension of repetitive DNA.
topic i-motif
DNA quadruplex structures
transcription regulation
cancer therapeutics
url https://www.mdpi.com/1424-8247/14/2/96
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