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Born for fairness: evidence of genetic contribution to a neural basis of fairness intuition.

ABSTRACT: Human beings often curb self-interest to develop and enforce social norms, such as fairness, as exemplified in the ultimatum game (UG). Inspired by the dual-system account for the responder's choice during the UG, we investigated whether the neural basis of psychological process induced by fairness is under genetic control using a twin fMRI study (62 monozygotic, 48 dizygotic; mean age: 19.32?±?1.38 years). We found a moderate genetic contribution to the rejection rate of unfair proposals (24%-35%), independent of stake size or proposer type, during the UG. Using a voxel-level analysis, we found that genetic factors moderately contributed to unfairness-evoked activation in the bilateral anterior insula (AI), regions representing the intuition of fairness norm violations (mean heritability: left 37%, right 40%). No genetic contributions were found in regions related to deliberate, controlled processes in the UG. This study provides the first evidence that evoked brain activity by unfairness in the bilateral AI is influenced by genes and sheds light on the genetic basis of brain processes underlying costly punishment.

SUBMITTER: Wang Y

PROVIDER: S-EPMC6545531 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

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Born for fairness: evidence of genetic contribution to a neural basis of fairness intuition.

Wang Yun Y Zheng Dang D Chen Jie J Rao Li-Lin LL Li Shu S Zhou Yuan Y

Social cognitive and affective neuroscience 20190501 5

Human beings often curb self-interest to develop and enforce social norms, such as fairness, as exemplified in the ultimatum game (UG). Inspired by the dual-system account for the responder's choice during the UG, we investigated whether the neural basis of psychological process induced by fairness is under genetic control using a twin fMRI study (62 monozygotic, 48 dizygotic; mean age: 19.32 ± 1.38 years). We found a moderate genetic contribution to the rejection rate of unfair proposals (24%-3 ...[more]

PMID: 31034055

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Project description:OBJECTIVE:Recombinant inbred mouse strains generated from an LG/J and SM/J intercross offer a unique resource to study complex genetic traits such as osteoarthritis (OA). We undertook this study to determine the susceptibility of 14 strains to various phenotypes characteristic of posttraumatic OA. We hypothesized that phenotypic variability is associated with genetic variability. METHODS:Ten-week-old male mice underwent surgical destabilization of the medial meniscus (DMM) to induce posttraumatic OA. Mice were killed 8 weeks after surgery, and knee joints were processed for histology to score cartilage degeneration and synovitis. Micro-computed tomography was used to analyze trabecular bone parameters including subchondral bone plate thickness and synovial ectopic calcifications. Gene expression in the knees was assessed using a QuantiGene Plex assay. RESULTS:Broad-sense heritability ranged from 0.18 to 0.58, which suggested that the responses to surgery were moderately heritable. The LGXSM-33, LGXSM-5, LGXSM-46, and SM/J strains were highly susceptible to OA, while the LGXSM-131b, LGXSM-163, LGXSM-35, LGXSM-128a, LGXSM-6, and LG/J strains were relatively OA resistant. This study was the first to accomplish measurement of genetic correlations of phenotypes that are characteristic of posttraumatic OA. Cartilage degeneration was significantly positively associated with synovitis (r = 0.83-0.92), and subchondral bone plate thickness was negatively correlated with ectopic calcifications (r = -0.59). Moreover, we showed that 40 of the 78 genes tested were significantly correlated with various OA phenotypes. However, unlike the OA phenotypes, there was no evidence for genetic variation in differences in gene expression levels between DMM-operated and sham-operated knees. CONCLUSION:For these mouse strains, various characteristics of posttraumatic OA varied with genetic composition, which demonstrated a genetic basis for susceptibility to posttraumatic OA. The heritability of posttraumatic OA was established. Phenotypes exhibited various degrees of correlations; cartilage degeneration was positively correlated with synovitis, but not with the formation of ectopic calcifications. Further investigation of the genome regions that contain genes implicated in OA, as well as further investigation of gene expression data, will be useful for studying mechanisms of OA and identifying therapeutic targets.

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Born for fairness: evidence of genetic contribution to a neural basis of fairness intuition.

Publications

Born for fairness: evidence of genetic contribution to a neural basis of fairness intuition.

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