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Candidate SNP markers of changes in the expression levels of the human SCN9A gene as a hub gene for pain generation, perception, response and anesthesia. / Dotsenko, P. A.; Zolotareva, K. A.; Ivanov, R. A. и др.

в: Vavilovskii Zhurnal Genetiki i Selektsii, Том 28, № 8, 12.2024, стр. 808-821.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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APA

Vancouver

Dotsenko PA, Zolotareva KA, Ivanov RA, Chadaeva IV, Podkolodnyy NL, Ivanisenko VA и др. Candidate SNP markers of changes in the expression levels of the human SCN9A gene as a hub gene for pain generation, perception, response and anesthesia. Vavilovskii Zhurnal Genetiki i Selektsii. 2024 дек.;28(8):808-821. doi: 10.18699/vjgb-24-89

Author

Dotsenko, P. A. ; Zolotareva, K. A. ; Ivanov, R. A. и др. / Candidate SNP markers of changes in the expression levels of the human SCN9A gene as a hub gene for pain generation, perception, response and anesthesia. в: Vavilovskii Zhurnal Genetiki i Selektsii. 2024 ; Том 28, № 8. стр. 808-821.

BibTeX

@article{2b5e3740aa884b319991b0326e0f30df,
title = "Candidate SNP markers of changes in the expression levels of the human SCN9A gene as a hub gene for pain generation, perception, response and anesthesia",
abstract = "In this work, we for the first time performed a comprehensive bioinformatics analysis of 568 human genes that, according to the NCBI Gene database as on September 15, 2024, were associated with pain generation, perception and anesthesia. The SCN9A gene encoding the sodium voltage-gated channel α subunit 9 and expressed in sensory neurons for transferring signals to the central nervous system about tissue damage was the only one involved in all the processes of interest at once as a hub gene. First, with our tool called OrthoWeb, we estimated the phylostratigraphic age indices (PAIs) for each of the genes, that is, identified the taxon of the most recent common ancestor of the organisms for which that gene has been sequenced. The mean PAI for all genes under study, including SCN9A as a hub gene for pain generation, perception, response and anesthesia, was {\textquoteleft}4{\textquoteright}. On the evolutionary scale by the Kyoto Encyclopedia of Genes and Genomes (KEGG), the ancestor is the phylum Chordata, some of the most ancient of which evolved the central and the peripheral nervous system. Next, with our tool called ANDSystem, we found that phosphorylation of ion channels is a centerpiece in pain generation, perception, response and anesthesia, on which the efficiency of signal transduction from the peripheral to the central system depends. This conclusion was consistent with literature data on a key role an efficient signal transduction from the peripheral to the central system from the peripheral to the central system for adjusting the human circadian rhythm through detection of a change from the dark of night to the light of day and for identification of the direction of the source of sound by auditory brainstem nuclei, for generating the response to cold stress and for physical coordination. 21 candidate SNP marker of significant SCN9A over- and underexpression. Finally, the ratio of SCN9A upregulating to downregulating SNPs was compared to that for all known human genes estimated by the 1000 Genomes Project Consortium. It was found that SCN9A as a hub gene for pain generation, perception, pain response and anesthesia is acted on by natural selection against its downregulation, to keep the nervous system highly informed on the status of the organism and the environment.",
keywords = "SCN9A, SNP, TBP, anesthesia, expression change, hub gene, human, pain generation, pain perception, pain response, promoter",
author = "Dotsenko, {P. A.} and Zolotareva, {K. A.} and Ivanov, {R. A.} and Chadaeva, {I. V.} and Podkolodnyy, {N. L.} and Ivanisenko, {V. A.} and Demenkov, {P. S.} and Lashin, {S. A.} and Ponomarenko, {M. P.}",
note = "This work was funded by the Russian Federal Science and Technology Program for the Development of Genetic Technologies. The authors are grateful to the Shared Center “Bioinformatics” for access to computing resources under Budget Project FWNR-2022-0020.",
year = "2024",
month = dec,
doi = "10.18699/vjgb-24-89",
language = "English",
volume = "28",
pages = "808--821",
journal = "Вавиловский журнал генетики и селекции",
issn = "2500-0462",
publisher = "Institute of Cytology and Genetics of Siberian Branch of the Russian Academy of Sciences",
number = "8",

}

RIS

TY - JOUR

T1 - Candidate SNP markers of changes in the expression levels of the human SCN9A gene as a hub gene for pain generation, perception, response and anesthesia

AU - Dotsenko, P. A.

AU - Zolotareva, K. A.

AU - Ivanov, R. A.

AU - Chadaeva, I. V.

AU - Podkolodnyy, N. L.

AU - Ivanisenko, V. A.

AU - Demenkov, P. S.

AU - Lashin, S. A.

AU - Ponomarenko, M. P.

N1 - This work was funded by the Russian Federal Science and Technology Program for the Development of Genetic Technologies. The authors are grateful to the Shared Center “Bioinformatics” for access to computing resources under Budget Project FWNR-2022-0020.

PY - 2024/12

Y1 - 2024/12

N2 - In this work, we for the first time performed a comprehensive bioinformatics analysis of 568 human genes that, according to the NCBI Gene database as on September 15, 2024, were associated with pain generation, perception and anesthesia. The SCN9A gene encoding the sodium voltage-gated channel α subunit 9 and expressed in sensory neurons for transferring signals to the central nervous system about tissue damage was the only one involved in all the processes of interest at once as a hub gene. First, with our tool called OrthoWeb, we estimated the phylostratigraphic age indices (PAIs) for each of the genes, that is, identified the taxon of the most recent common ancestor of the organisms for which that gene has been sequenced. The mean PAI for all genes under study, including SCN9A as a hub gene for pain generation, perception, response and anesthesia, was ‘4’. On the evolutionary scale by the Kyoto Encyclopedia of Genes and Genomes (KEGG), the ancestor is the phylum Chordata, some of the most ancient of which evolved the central and the peripheral nervous system. Next, with our tool called ANDSystem, we found that phosphorylation of ion channels is a centerpiece in pain generation, perception, response and anesthesia, on which the efficiency of signal transduction from the peripheral to the central system depends. This conclusion was consistent with literature data on a key role an efficient signal transduction from the peripheral to the central system from the peripheral to the central system for adjusting the human circadian rhythm through detection of a change from the dark of night to the light of day and for identification of the direction of the source of sound by auditory brainstem nuclei, for generating the response to cold stress and for physical coordination. 21 candidate SNP marker of significant SCN9A over- and underexpression. Finally, the ratio of SCN9A upregulating to downregulating SNPs was compared to that for all known human genes estimated by the 1000 Genomes Project Consortium. It was found that SCN9A as a hub gene for pain generation, perception, pain response and anesthesia is acted on by natural selection against its downregulation, to keep the nervous system highly informed on the status of the organism and the environment.

AB - In this work, we for the first time performed a comprehensive bioinformatics analysis of 568 human genes that, according to the NCBI Gene database as on September 15, 2024, were associated with pain generation, perception and anesthesia. The SCN9A gene encoding the sodium voltage-gated channel α subunit 9 and expressed in sensory neurons for transferring signals to the central nervous system about tissue damage was the only one involved in all the processes of interest at once as a hub gene. First, with our tool called OrthoWeb, we estimated the phylostratigraphic age indices (PAIs) for each of the genes, that is, identified the taxon of the most recent common ancestor of the organisms for which that gene has been sequenced. The mean PAI for all genes under study, including SCN9A as a hub gene for pain generation, perception, response and anesthesia, was ‘4’. On the evolutionary scale by the Kyoto Encyclopedia of Genes and Genomes (KEGG), the ancestor is the phylum Chordata, some of the most ancient of which evolved the central and the peripheral nervous system. Next, with our tool called ANDSystem, we found that phosphorylation of ion channels is a centerpiece in pain generation, perception, response and anesthesia, on which the efficiency of signal transduction from the peripheral to the central system depends. This conclusion was consistent with literature data on a key role an efficient signal transduction from the peripheral to the central system from the peripheral to the central system for adjusting the human circadian rhythm through detection of a change from the dark of night to the light of day and for identification of the direction of the source of sound by auditory brainstem nuclei, for generating the response to cold stress and for physical coordination. 21 candidate SNP marker of significant SCN9A over- and underexpression. Finally, the ratio of SCN9A upregulating to downregulating SNPs was compared to that for all known human genes estimated by the 1000 Genomes Project Consortium. It was found that SCN9A as a hub gene for pain generation, perception, pain response and anesthesia is acted on by natural selection against its downregulation, to keep the nervous system highly informed on the status of the organism and the environment.

KW - SCN9A

KW - SNP

KW - TBP

KW - anesthesia

KW - expression change

KW - hub gene

KW - human

KW - pain generation

KW - pain perception

KW - pain response

KW - promoter

UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85217108302&origin=inward&txGid=5ecf2199afa85ff30df8080a9c038978

UR - https://www.mendeley.com/catalogue/43d13730-68f6-3c72-817d-3c2f19a50acc/

U2 - 10.18699/vjgb-24-89

DO - 10.18699/vjgb-24-89

M3 - Article

C2 - 39944808

VL - 28

SP - 808

EP - 821

JO - Вавиловский журнал генетики и селекции

JF - Вавиловский журнал генетики и селекции

SN - 2500-0462

IS - 8

ER -

ID: 64715163