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Natural selection equally supports the human tendencies in subordination and domination : A Genome-wide study with in silico confirmation and in vivo validation in mice. / Chadaeva, Irina; Ponomarenko, Petr; Rasskazov, Dmitry et al.

In: Frontiers in Genetics, Vol. 10, No. FEB, 73, 20.02.2019.

Research output: Contribution to journalArticlepeer-review

Harvard

Chadaeva, I, Ponomarenko, P, Rasskazov, D, Sharypova, E, Kashina, E, Kleshchev, M, Ponomarenko, M, Naumenko, V, Savinkova, L, Kolchanov, N, Osadchuk, L & Osadchuk, A 2019, 'Natural selection equally supports the human tendencies in subordination and domination: A Genome-wide study with in silico confirmation and in vivo validation in mice', Frontiers in Genetics, vol. 10, no. FEB, 73. https://doi.org/10.3389/fgene.2019.00073

APA

Chadaeva, I., Ponomarenko, P., Rasskazov, D., Sharypova, E., Kashina, E., Kleshchev, M., Ponomarenko, M., Naumenko, V., Savinkova, L., Kolchanov, N., Osadchuk, L., & Osadchuk, A. (2019). Natural selection equally supports the human tendencies in subordination and domination: A Genome-wide study with in silico confirmation and in vivo validation in mice. Frontiers in Genetics, 10(FEB), [73]. https://doi.org/10.3389/fgene.2019.00073

Vancouver

Chadaeva I, Ponomarenko P, Rasskazov D, Sharypova E, Kashina E, Kleshchev M et al. Natural selection equally supports the human tendencies in subordination and domination: A Genome-wide study with in silico confirmation and in vivo validation in mice. Frontiers in Genetics. 2019 Feb 20;10(FEB):73. doi: 10.3389/fgene.2019.00073

Author

Chadaeva, Irina ; Ponomarenko, Petr ; Rasskazov, Dmitry et al. / Natural selection equally supports the human tendencies in subordination and domination : A Genome-wide study with in silico confirmation and in vivo validation in mice. In: Frontiers in Genetics. 2019 ; Vol. 10, No. FEB.

BibTeX

@article{be466436b1654dae9b1a66738419ddd9,
title = "Natural selection equally supports the human tendencies in subordination and domination: A Genome-wide study with in silico confirmation and in vivo validation in mice",
abstract = "We proposed the following heuristic decision-making rule: {"}IF {an excess of a protein relating to the nervous system is an experimentally known physiological marker of low pain sensitivity, fast postinjury recovery, or aggressive, risk/novelty-seeking, anesthetic-like, or similar agonistic-intolerant behavior} AND IF {a single nucleotide polymorphism (SNP) causes overexpression of the gene encoding this protein} THEN {this SNP can be a SNP marker of the tendency in dominance} WHILE {underexpression corresponds to subordination} AND vice versa.{"} Using this decision-making rule, we analyzed 231 human genes of neuropeptidergic, non-neuropeptidergic, and neurotrophinergic systems that encode neurotrophic and growth factors, interleukins, neurotransmitters, receptors, transporters, and enzymes. These proteins are known as key factors of human social behavior. We analyzed all the 5,052 SNPs within the 70 bp promoter region upstream of the position where the protein-coding transcript starts, which were retrieved from databases Ensembl and dbSNP using our previously created public Web service SNP-TATA-Comparator (http://beehive.bionet.nsc.ru/cgi-bin/mgs/tatascan/start.pl). This definition of the promoter region includes all TATA-binding protein (TBP)-binding sites. A total of 556 and 552 candidate SNP markers contributing to the dominance and the subordination, respectively, were uncovered. On this basis, we determined that 231 human genes under study are subject to natural selection against underexpression (significance p < 0.0005), which equally supports the human tendencies in domination and subordination such as the norm of a reaction (plasticity) of the human social hierarchy. These findings explain vertical transmission of domination and subordination traits previously observed in rodent models. Thus, the results of this study equally support both sides of the century-old unsettled scientific debate on whether both aggressiveness and the social hierarchy among humans are inherited (as suggested by Freud and Lorenz) or are due to non-genetic social education, when the children are influenced by older individuals across generations (as proposed by Berkowitz and Fromm).",
keywords = "Candidate Snp Marker, Expression Change, Gene, Promoter, Snp, Social Hierarchy, Tata-Box, Tbp",
author = "Irina Chadaeva and Petr Ponomarenko and Dmitry Rasskazov and Ekaterina Sharypova and Elena Kashina and Maxim Kleshchev and Mikhail Ponomarenko and Vladimir Naumenko and Ludmila Savinkova and Nikolay Kolchanov and Ludmila Osadchuk and Alexandr Osadchuk",
year = "2019",
month = feb,
day = "20",
doi = "10.3389/fgene.2019.00073",
language = "English",
volume = "10",
journal = "Frontiers in Genetics",
issn = "1664-8021",
publisher = "Frontiers Media S.A.",
number = "FEB",

}

RIS

TY - JOUR

T1 - Natural selection equally supports the human tendencies in subordination and domination

T2 - A Genome-wide study with in silico confirmation and in vivo validation in mice

AU - Chadaeva, Irina

AU - Ponomarenko, Petr

AU - Rasskazov, Dmitry

AU - Sharypova, Ekaterina

AU - Kashina, Elena

AU - Kleshchev, Maxim

AU - Ponomarenko, Mikhail

AU - Naumenko, Vladimir

AU - Savinkova, Ludmila

AU - Kolchanov, Nikolay

AU - Osadchuk, Ludmila

AU - Osadchuk, Alexandr

PY - 2019/2/20

Y1 - 2019/2/20

N2 - We proposed the following heuristic decision-making rule: "IF {an excess of a protein relating to the nervous system is an experimentally known physiological marker of low pain sensitivity, fast postinjury recovery, or aggressive, risk/novelty-seeking, anesthetic-like, or similar agonistic-intolerant behavior} AND IF {a single nucleotide polymorphism (SNP) causes overexpression of the gene encoding this protein} THEN {this SNP can be a SNP marker of the tendency in dominance} WHILE {underexpression corresponds to subordination} AND vice versa." Using this decision-making rule, we analyzed 231 human genes of neuropeptidergic, non-neuropeptidergic, and neurotrophinergic systems that encode neurotrophic and growth factors, interleukins, neurotransmitters, receptors, transporters, and enzymes. These proteins are known as key factors of human social behavior. We analyzed all the 5,052 SNPs within the 70 bp promoter region upstream of the position where the protein-coding transcript starts, which were retrieved from databases Ensembl and dbSNP using our previously created public Web service SNP-TATA-Comparator (http://beehive.bionet.nsc.ru/cgi-bin/mgs/tatascan/start.pl). This definition of the promoter region includes all TATA-binding protein (TBP)-binding sites. A total of 556 and 552 candidate SNP markers contributing to the dominance and the subordination, respectively, were uncovered. On this basis, we determined that 231 human genes under study are subject to natural selection against underexpression (significance p < 0.0005), which equally supports the human tendencies in domination and subordination such as the norm of a reaction (plasticity) of the human social hierarchy. These findings explain vertical transmission of domination and subordination traits previously observed in rodent models. Thus, the results of this study equally support both sides of the century-old unsettled scientific debate on whether both aggressiveness and the social hierarchy among humans are inherited (as suggested by Freud and Lorenz) or are due to non-genetic social education, when the children are influenced by older individuals across generations (as proposed by Berkowitz and Fromm).

AB - We proposed the following heuristic decision-making rule: "IF {an excess of a protein relating to the nervous system is an experimentally known physiological marker of low pain sensitivity, fast postinjury recovery, or aggressive, risk/novelty-seeking, anesthetic-like, or similar agonistic-intolerant behavior} AND IF {a single nucleotide polymorphism (SNP) causes overexpression of the gene encoding this protein} THEN {this SNP can be a SNP marker of the tendency in dominance} WHILE {underexpression corresponds to subordination} AND vice versa." Using this decision-making rule, we analyzed 231 human genes of neuropeptidergic, non-neuropeptidergic, and neurotrophinergic systems that encode neurotrophic and growth factors, interleukins, neurotransmitters, receptors, transporters, and enzymes. These proteins are known as key factors of human social behavior. We analyzed all the 5,052 SNPs within the 70 bp promoter region upstream of the position where the protein-coding transcript starts, which were retrieved from databases Ensembl and dbSNP using our previously created public Web service SNP-TATA-Comparator (http://beehive.bionet.nsc.ru/cgi-bin/mgs/tatascan/start.pl). This definition of the promoter region includes all TATA-binding protein (TBP)-binding sites. A total of 556 and 552 candidate SNP markers contributing to the dominance and the subordination, respectively, were uncovered. On this basis, we determined that 231 human genes under study are subject to natural selection against underexpression (significance p < 0.0005), which equally supports the human tendencies in domination and subordination such as the norm of a reaction (plasticity) of the human social hierarchy. These findings explain vertical transmission of domination and subordination traits previously observed in rodent models. Thus, the results of this study equally support both sides of the century-old unsettled scientific debate on whether both aggressiveness and the social hierarchy among humans are inherited (as suggested by Freud and Lorenz) or are due to non-genetic social education, when the children are influenced by older individuals across generations (as proposed by Berkowitz and Fromm).

KW - Candidate Snp Marker

KW - Expression Change

KW - Gene

KW - Promoter

KW - Snp

KW - Social Hierarchy

KW - Tata-Box

KW - Tbp

UR - http://www.scopus.com/inward/record.url?scp=85065980355&partnerID=8YFLogxK

U2 - 10.3389/fgene.2019.00073

DO - 10.3389/fgene.2019.00073

M3 - Article

C2 - 30873204

AN - SCOPUS:85065980355

VL - 10

JO - Frontiers in Genetics

JF - Frontiers in Genetics

SN - 1664-8021

IS - FEB

M1 - 73

ER -

ID: 23544733