Detection of DNA methylation profile changes using FTIR micro-spectroscopy: a method for possible implementation as a diagnostic tool in diabetes, ALBA Synchrotron, BL01 – MIRAS, Project No.: 2018093034

Link to this page

Detection of DNA methylation profile changes using FTIR micro-spectroscopy: a method for possible implementation as a diagnostic tool in diabetes, ALBA Synchrotron, BL01 – MIRAS, Project No.: 2018093034

Authors

Publications

Detection of DNA methylation profiles in mouse embryonic fibroblasts using Fourier transform-infrared spectroscopy

Sarić, Ana; Tolić, Anja; Grdović, Nevena; Dinić, Svetlana; Rajić, Jovana; Đorđević, Miloš; Đorđević, Marija; Arambašić Jovanović, Jelena; Mihailović, Mirjana; Poznanović, Goran; Uskoković, Aleksandra; Vidaković, Melita; Dučić, Tanja

(Belgrade: Serbian Genetic Society, 2019)

TY  - CONF
AU  - Sarić, Ana
AU  - Tolić, Anja
AU  - Grdović, Nevena
AU  - Dinić, Svetlana
AU  - Rajić, Jovana
AU  - Đorđević, Miloš
AU  - Đorđević, Marija
AU  - Arambašić Jovanović, Jelena
AU  - Mihailović, Mirjana
AU  - Poznanović, Goran
AU  - Uskoković, Aleksandra
AU  - Vidaković, Melita
AU  - Dučić, Tanja
PY  - 2019
UR  - http://radar.ibiss.bg.ac.rs/handle/123456789/5694
AB  - Epigenetic processes orchestrate the cell type-specific use of the genetic information
essential for normal development and for maintaining the overall integrity of the genome.
DNA methylation is probably the most extensively studied epigenetic mark and represents
the covalent attachment of a methyl group to cytosine that is located next to guanine within
the genomic DNA. The alteration of DNA methylation patterns by hyperglycaemia, oxidative
stress and inflammation may have potential epigenetic impacts on gene regulation in diabetic
individuals. Further research devoted to improve the steps that could be undertaken in the
early diagnosis, prevention and treatment of diabetes and its complications is a scientifically
and socially significant task. We used the Fourier transform-infrared (FTIR) spectroscopy
(ALBA synchrotron, Cerdanyola del valles, Spain) for qualitative spectral analysis of
normomethylated DNA from mouse fibroblast cells (NIH3T3) and hypomethylated DNA
from PARP-1 knockout mouse fibroblast cells (PARP-/-). We obtained the global information
regarding the DNA methylation profiles in mouse fibroblast cells by FTIR spectroscopy that
was visualised by immune-fluorescent staining using anti-methyl cytosine (5mC) antibody.
Some differences in DNA methylation profiles between examined cell lines were observed
in spectral region significant for cytosine (990-1250 nm). The most interesting picks were
observed approximately at wavelength: 1240 nm, 1150 nm, 1110 nm and 1010 nm. These
results are in the same time a verification of the proof of principle for FTIR based analysis of
the differences between normomethylated and hypomethylated genomic DNA which could
be set as a potential predictive and diagnostic tool in future. To our knowledge this is a first
time that synchrotron-based FTIR micro-spectroscopy is used for detection of the presence
of 5mC and changes in the DNA methylation profile in cells.
PB  - Belgrade: Serbian Genetic Society
C3  - 6th Congress of the Serbian genetic society: Book of abstracts; 2019 Oct 13-17; Vrnjačka Banja, Serbia
T1  - Detection of DNA methylation profiles in mouse embryonic fibroblasts using Fourier transform-infrared spectroscopy
SP  - 75
UR  - https://hdl.handle.net/21.15107/rcub_ibiss_5694
ER  - 
@conference{
author = "Sarić, Ana and Tolić, Anja and Grdović, Nevena and Dinić, Svetlana and Rajić, Jovana and Đorđević, Miloš and Đorđević, Marija and Arambašić Jovanović, Jelena and Mihailović, Mirjana and Poznanović, Goran and Uskoković, Aleksandra and Vidaković, Melita and Dučić, Tanja",
year = "2019",
abstract = "Epigenetic processes orchestrate the cell type-specific use of the genetic information
essential for normal development and for maintaining the overall integrity of the genome.
DNA methylation is probably the most extensively studied epigenetic mark and represents
the covalent attachment of a methyl group to cytosine that is located next to guanine within
the genomic DNA. The alteration of DNA methylation patterns by hyperglycaemia, oxidative
stress and inflammation may have potential epigenetic impacts on gene regulation in diabetic
individuals. Further research devoted to improve the steps that could be undertaken in the
early diagnosis, prevention and treatment of diabetes and its complications is a scientifically
and socially significant task. We used the Fourier transform-infrared (FTIR) spectroscopy
(ALBA synchrotron, Cerdanyola del valles, Spain) for qualitative spectral analysis of
normomethylated DNA from mouse fibroblast cells (NIH3T3) and hypomethylated DNA
from PARP-1 knockout mouse fibroblast cells (PARP-/-). We obtained the global information
regarding the DNA methylation profiles in mouse fibroblast cells by FTIR spectroscopy that
was visualised by immune-fluorescent staining using anti-methyl cytosine (5mC) antibody.
Some differences in DNA methylation profiles between examined cell lines were observed
in spectral region significant for cytosine (990-1250 nm). The most interesting picks were
observed approximately at wavelength: 1240 nm, 1150 nm, 1110 nm and 1010 nm. These
results are in the same time a verification of the proof of principle for FTIR based analysis of
the differences between normomethylated and hypomethylated genomic DNA which could
be set as a potential predictive and diagnostic tool in future. To our knowledge this is a first
time that synchrotron-based FTIR micro-spectroscopy is used for detection of the presence
of 5mC and changes in the DNA methylation profile in cells.",
publisher = "Belgrade: Serbian Genetic Society",
journal = "6th Congress of the Serbian genetic society: Book of abstracts; 2019 Oct 13-17; Vrnjačka Banja, Serbia",
title = "Detection of DNA methylation profiles in mouse embryonic fibroblasts using Fourier transform-infrared spectroscopy",
pages = "75",
url = "https://hdl.handle.net/21.15107/rcub_ibiss_5694"
}
Sarić, A., Tolić, A., Grdović, N., Dinić, S., Rajić, J., Đorđević, M., Đorđević, M., Arambašić Jovanović, J., Mihailović, M., Poznanović, G., Uskoković, A., Vidaković, M.,& Dučić, T.. (2019). Detection of DNA methylation profiles in mouse embryonic fibroblasts using Fourier transform-infrared spectroscopy. in 6th Congress of the Serbian genetic society: Book of abstracts; 2019 Oct 13-17; Vrnjačka Banja, Serbia
Belgrade: Serbian Genetic Society., 75.
https://hdl.handle.net/21.15107/rcub_ibiss_5694
Sarić A, Tolić A, Grdović N, Dinić S, Rajić J, Đorđević M, Đorđević M, Arambašić Jovanović J, Mihailović M, Poznanović G, Uskoković A, Vidaković M, Dučić T. Detection of DNA methylation profiles in mouse embryonic fibroblasts using Fourier transform-infrared spectroscopy. in 6th Congress of the Serbian genetic society: Book of abstracts; 2019 Oct 13-17; Vrnjačka Banja, Serbia. 2019;:75.
https://hdl.handle.net/21.15107/rcub_ibiss_5694 .
Sarić, Ana, Tolić, Anja, Grdović, Nevena, Dinić, Svetlana, Rajić, Jovana, Đorđević, Miloš, Đorđević, Marija, Arambašić Jovanović, Jelena, Mihailović, Mirjana, Poznanović, Goran, Uskoković, Aleksandra, Vidaković, Melita, Dučić, Tanja, "Detection of DNA methylation profiles in mouse embryonic fibroblasts using Fourier transform-infrared spectroscopy" in 6th Congress of the Serbian genetic society: Book of abstracts; 2019 Oct 13-17; Vrnjačka Banja, Serbia (2019):75,
https://hdl.handle.net/21.15107/rcub_ibiss_5694 .