Emotion recognition associated with polymorphism in oxytocinergic pathway gene ARNT2

被引:15
|
作者
Hovey, Daniel [1 ]
Henningsson, Susanne [1 ]
Cortes, Diana S. [2 ]
Banziger, Tanja [3 ]
Zettergren, Anna [1 ,4 ]
Melke, Jonas [1 ]
Fischer, Hakan [2 ]
Laukka, Petri [2 ]
Westberg, Lars [1 ]
机构
[1] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Pharmacol, Box 431, S-40530 Gothenburg, Sweden
[2] Stockholm Univ, Dept Psychol, Stockholm, Sweden
[3] Mid Sweden Univ, Dept Psychol, Ostersund, Sweden
[4] Univ Gothenburg, Sahlgrenska Acad, Inst Neurosci & Physiol, Dept Psychiat & Neurochem, Gothenburg, Sweden
基金
瑞典研究理事会;
关键词
oxytocin; vasopressin; ARNT2; emotion recognition; social cognition; AUTISM SPECTRUM DISORDER; TORONTO-ALEXITHYMIA-SCALE; RECEPTOR OXTR GENE; SEX-DIFFERENCES; INDIVIDUAL-DIFFERENCES; AGGRESSIVE-BEHAVIOR; BRAIN ACTIVATION; CROSS-VALIDATION; FACIAL MIMICRY; AVPR1A GENE;
D O I
10.1093/scan/nsx141
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ability to correctly understand the emotional expression of another person is essential for social relationships and appears to be a partly inherited trait. The neuropeptides oxytocin and vasopressin have been shown to influence this ability as well as face processing in humans. Here, recognition of the emotional content of faces and voices, separately and combined, was investigated in 492 subjects, genotyped for 25 single nucleotide polymorphisms (SNPs) in eight genes encoding proteins important for oxytocin and vasopressin neurotransmission. The SNP rs4778599 in the gene encoding aryl hydrocarbon receptor nuclear translocator 2 (ARNT2), a transcription factor that participates in the development of hypothalamic oxytocin and vasopressin neurons, showed an association that survived correction for multiple testing with emotion recognition of audio-visual stimuli in women (). This study demonstrates evidence for an association that further expands previous findings of oxytocin and vasopressin involvement in emotion recognition.
引用
收藏
页码:173 / 181
页数:9
相关论文
共 50 条
  • [1] Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
    Di Napoli, Agnese
    Warrier, Varun
    Baron-Cohen, Simon
    Chakrabarti, Bhismadev
    MOLECULAR AUTISM, 2015, 6
  • [2] Genetic variant rs17225178 in the ARNT2 gene is associated with Asperger Syndrome
    Agnese Di Napoli
    Varun Warrier
    Simon Baron-Cohen
    Bhismadev Chakrabarti
    Molecular Autism, 6
  • [3] ARNT gene multiplicity in amphibians: Characterization of ARNT2 from the frog Xenopus laevis
    Rowatt, AJ
    Depowell, JJ
    Powell, WH
    JOURNAL OF EXPERIMENTAL ZOOLOGY PART B-MOLECULAR AND DEVELOPMENTAL EVOLUTION, 2003, 300B (01) : 48 - 57
  • [5] Targeted mutation of the murine arylhydrocarbon receptor nuclear translocator 2 (Arnt2) gene reveals partial redundancy with Arnt
    Keith, B
    Adelman, DM
    Simon, MC
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (12) : 6692 - 6697
  • [6] Overexpression of ARNT2 is associated with decreased cell proliferation and better prognosis in gastric cancer
    Jia, Yanfei
    Hao, Shuhua
    Jin, Guangchao
    Li, Hongyu
    Ma, Xiaoli
    Zheng, Yan
    Xiao, Dongjie
    Wang, Yunshan
    MOLECULAR AND CELLULAR BIOCHEMISTRY, 2019, 450 (1-2) : 97 - 103
  • [7] Overexpression of ARNT2 is associated with decreased cell proliferation and better prognosis in gastric cancer
    Yanfei Jia
    Shuhua Hao
    Guangchao Jin
    Hongyu Li
    Xiaoli Ma
    Yan Zheng
    Dongjie Xiao
    Yunshan Wang
    Molecular and Cellular Biochemistry, 2019, 450 : 97 - 103
  • [8] ARNT2 is downregulated and serves as a potential tumor suppressor gene in non-small cell lung cancer
    Yang, Bo
    Yang, Ende
    Liao, Hehe
    Wang, Zhouquan
    Den, Zhiping
    Ren, Hong
    TUMOR BIOLOGY, 2015, 36 (03) : 2111 - 2119
  • [9] Webb-Dattani Syndrome: Report of a Saudi Arabian Family with a Novel Homozygous Mutation in the ARNT2 Gene
    Al-Sannaa, Nouriya Abbas
    Pepler, Alexander
    Al-Abdulwahed, Hind Y.
    Al-Majed, Sami I.
    Abdi, Rifat F.
    Menzel, Moritz
    Biskup, Saskia
    JOURNAL OF PEDIATRIC NEUROLOGY, 2019, 17 (02) : 71 - 76
  • [10] Polymorphisms within the ARNT2 and CX3CR1 Genes Are Associated with the Risk of Developing Invasive Aspergillosis
    Lupianez, C. B.
    Martinez-Bueno, M.
    Sanchez-Maldonado, J. M.
    Badiola, J.
    Cunha, C.
    Springer, J.
    Lackner, M.
    Segura-Catena, J.
    Canet, L. M.
    Alcazar-Fuoli, L.
    Lopez-Nevot, M. A.
    Fianchi, L.
    Aguado, J. M.
    Pagano, L.
    Lopez-Fernandez, E.
    Alarcon-Riquelme, M.
    Potenza, L.
    Goncalves, S. M.
    Luppi, M.
    Moratalla, L.
    Solano, C.
    Sampedro, A.
    Gonzalez-Sierra, P.
    Cuenca-Estrella, M.
    Lagrou, K.
    Maertens, J. A.
    Lass-Floerl, C.
    Einsele, H.
    Vazquez, L.
    Loeffler, J.
    Rios-Tamayo, R.
    Carvalho, A.
    Jurado, M.
    Sainz, J.
    INFECTION AND IMMUNITY, 2020, 88 (04)