Journal of the American Chemical Society, volume 136, issue 11, pages 4161-4171

The Dynamic Character of the BCL2 Promoter i-Motif Provides a Mechanism for Modulation of Gene Expression by Compounds That Bind Selectively to the Alternative DNA Hairpin Structure

Hyun Jin Kang 2
Varghese John 3
Manikandadas M Madathil 3
Prashansa Agrawal 2
Vijay Gokhale 4
Danzhou Yang 1
Sidney M. Hecht 5
Laurence H. Hurley 1
Publication typeJournal Article
Publication date2014-03-07
Quartile SCImago
Q1
Quartile WOS
Q1
Impact factor15
ISSN00027863, 15205126
PubMed ID:  24559410
General Chemistry
Catalysis
Biochemistry
Colloid and Surface Chemistry
Abstract
It is generally accepted that DNA predominantly exists in duplex form in cells. However, under torsional stress imposed by active transcription, DNA can assume nonduplex structures. The BCL2 promoter region forms two different secondary DNA structures on opposite strands called the G-quadruplex and the i-motif. The i-motif is a highly dynamic structure that exists in equilibrium with a flexible hairpin species. Here we identify a pregnanol derivative and a class of piperidine derivatives that differentially modulate gene expression by stabilizing either the i-motif or the flexible hairpin species. Stabilization of the i-motif structure results in significant upregulation of the BCL2 gene and associated protein expression; in contrast, stabilization of the flexible hairpin species lowers BCL2 levels. The BCL2 levels reduced by the hairpin-binding compound led to chemosensitization to etoposide in both in vitro and in vivo models. Furthermore, we show antagonism between the two classes of compounds in solution and in cells. For the first time, our results demonstrate the principle of small molecule targeting of i-motif structures in vitro and in vivo to modulate gene expression.

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GOST Copy
Kendrick S. et al. The Dynamic Character of the BCL2 Promoter i-Motif Provides a Mechanism for Modulation of Gene Expression by Compounds That Bind Selectively to the Alternative DNA Hairpin Structure // Journal of the American Chemical Society. 2014. Vol. 136. No. 11. pp. 4161-4171.
GOST all authors (up to 50) Copy
Kendrick S., Kang H. J., John V., Madathil M. M., Agrawal P., Gokhale V., Yang D., Hecht S. M., Hurley L. H. The Dynamic Character of the BCL2 Promoter i-Motif Provides a Mechanism for Modulation of Gene Expression by Compounds That Bind Selectively to the Alternative DNA Hairpin Structure // Journal of the American Chemical Society. 2014. Vol. 136. No. 11. pp. 4161-4171.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.1021/ja410934b
UR - https://doi.org/10.1021/ja410934b
TI - The Dynamic Character of the BCL2 Promoter i-Motif Provides a Mechanism for Modulation of Gene Expression by Compounds That Bind Selectively to the Alternative DNA Hairpin Structure
T2 - Journal of the American Chemical Society
AU - Kang, Hyun Jin
AU - Madathil, Manikandadas M
AU - Agrawal, Prashansa
AU - Kendrick, Samantha
AU - John, Varghese
AU - Gokhale, Vijay
AU - Yang, Danzhou
AU - Hecht, Sidney M.
AU - Hurley, Laurence H.
PY - 2014
DA - 2014/03/07
PB - American Chemical Society (ACS)
SP - 4161-4171
IS - 11
VL - 136
PMID - 24559410
SN - 0002-7863
SN - 1520-5126
ER -
BibTex |
Cite this
BibTex Copy
@article{2014_Kendrick,
author = {Hyun Jin Kang and Manikandadas M Madathil and Prashansa Agrawal and Samantha Kendrick and Varghese John and Vijay Gokhale and Danzhou Yang and Sidney M. Hecht and Laurence H. Hurley},
title = {The Dynamic Character of the BCL2 Promoter i-Motif Provides a Mechanism for Modulation of Gene Expression by Compounds That Bind Selectively to the Alternative DNA Hairpin Structure},
journal = {Journal of the American Chemical Society},
year = {2014},
volume = {136},
publisher = {American Chemical Society (ACS)},
month = {mar},
url = {https://doi.org/10.1021/ja410934b},
number = {11},
pages = {4161--4171},
doi = {10.1021/ja410934b}
}
MLA
Cite this
MLA Copy
Kendrick, Samantha, et al. “The Dynamic Character of the BCL2 Promoter i-Motif Provides a Mechanism for Modulation of Gene Expression by Compounds That Bind Selectively to the Alternative DNA Hairpin Structure.” Journal of the American Chemical Society, vol. 136, no. 11, Mar. 2014, pp. 4161-4171. https://doi.org/10.1021/ja410934b.
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