Please use this identifier to cite or link to this item:
https://dspace.iiti.ac.in/handle/123456789/3995
Title: | Restoration of miRNA-149 Expression by TmPyP4 Induced Unfolding of Quadruplex within Its Precursor |
Authors: | Kumar, Amit |
Keywords: | Cell proliferation;Circular dichroism spectroscopy;Cytology;Dichroism;Diseases;Gene expression;Nuclear magnetic resonance spectroscopy;Polymerase chain reaction;Proteins;Thulium compounds;Ultraviolet visible spectroscopy;Cellular microenvironment;Concentration-dependent;G-quadruplex structure;Isothermal titration calorimetry;MCF-7 breast cancer cells;Nucleotide sequences;Post-transcriptional;UV visible spectroscopy;RNA;complementary DNA;guanine quadruplex;microRNA;microRNA 149;porphyrin;regulator protein;RNA precursor;unclassified drug;ZBTB2 protein;guanine quadruplex;microRNA;MIRN149 microRNA, human;photosensitizing agent;porphyrin;repressor protein;tetra(4-N-methylpyridyl)porphine;ZBTB2 protein, human;Article;cell assay;cell proliferation;chemical binding;circular dichroism;colony formation assay;concentration (parameter);controlled study;flow cytometry;gene expression;gene expression regulation;gene function;human;human cell;isothermal titration calorimetry;MCF-7 cell line;nuclear magnetic resonance spectroscopy;priority journal;reverse transcription polymerase chain reaction;RNA isolation;RNA structure;ultraviolet spectroscopy;upregulation;Western blotting;chemistry;conformation;drug effect;genetics;metabolism;tumor stem cell assay;Cell Proliferation;G-Quadruplexes;Gene Expression Regulation, Neoplastic;Humans;MCF-7 Cells;MicroRNAs;Nucleic Acid Conformation;Photosensitizing Agents;Porphyrins;Repressor Proteins;Tumor Stem Cell Assay |
Issue Date: | 2019 |
Publisher: | American Chemical Society |
Citation: | Ghosh, A., Ekka, M. K., Tawani, A., Kumar, A., Chakraborty, D., & Maiti, S. (2019). Restoration of miRNA-149 expression by TmPyP4 induced unfolding of quadruplex within its precursor. Biochemistry, 58(6), 514-525. doi:10.1021/acs.biochem.8b00880 |
Abstract: | Noncoding RNAs are functional RNA molecules that get transcribed from DNA but are not translated into proteins; yet, they can regulate gene expression at transcriptional and post-transcriptional levels. Secondary structures present within these RNAs play a major role in determining their nature of function. In the case of miRNAs, the precursor miRNA have a hairpin stem loop structure which is required for Dicer recognition and further maturation. Alternately, it might assume a G-quadruplex structure. The transition from hairpin to G-quadruplex depends upon the nucleotide sequence as well as the cellular microenvironment, and this might affect the miRNA maturation and other downstream activity. Formation of the G-quadruplex within precursor miRNA-149 has been shown to inhibit Dicer processing activity followed by suppression of miRNA-149 maturation in cancer cells. In this report, we show that suppression of cell proliferation by the upregulated miRNA-149 could be rescued by unfolding the G-quadruplex present in pre-miRNA-149 by TmPyP4 (Porphyrin) treatment. Using UV-visible spectroscopy, circular dichroism, and isothermal titration calorimetry, we observed that TmPyP4 binds strongly to G-quadruplex and unfolds it, which was further verified by NMR spectroscopy. In cellulo, qRT-PCR measurements of miRNA-149 in MCF-7 breast cancer cells showed concentration dependent enhancement of mature miRNA-149 upon treatment of TmPyP4. As a consequence of enhanced miRNA-149 activity, we also observe the reduction in miRNA-149 target protein ZBTB2 that eventually leads to reduced cell proliferation. Copyright © 2018 American Chemical Society. |
URI: | https://doi.org/10.1021/acs.biochem.8b00880 https://dspace.iiti.ac.in/handle/123456789/3995 |
ISSN: | 0006-2960 |
Type of Material: | Journal Article |
Appears in Collections: | Department of Biosciences and Biomedical Engineering |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.
Altmetric Badge: