4.6 Article

Integrative Analyses Followed by Functional Characterization Reveal TMEM180 as a Schizophrenia Risk Gene

Journal

SCHIZOPHRENIA BULLETIN
Volume 47, Issue 5, Pages 1364-1374

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/schbul/sbab032

Keywords

schizophrenia; TMEM180; integrative analysis gene expression; TWAS; eQTL

Categories

Funding

  1. National Nature Science Foundation of China [31722029, 31970561]
  2. Innovative Research Team of Science and Technology Department of Yunnan Province [2019HC004]
  3. Distinguished Young Scientists grant of the Yunnan Province [202001AV070006]

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Recent integrative analyses identified TMEM180 as a gene associated with schizophrenia risk through TWAS and SMR in East Asian populations. TMEM180 mRNA expression was significantly decreased in schizophrenia cases compared to controls, and its role in neurodevelopment and brain function was highlighted. Integration and sharing of resources in biomedical research are essential in the big data era.
Recent large-scale integrative analyses (including Transcriptome-Wide Association Study [TWAS] and Summary-data-based Mendelian Randomization [SMR]) have identified multiple genes whose cis-regulated expression changes may confer risk of schizophrenia. Nevertheless, expression quantitative trait loci (eQTL) data and genome-wide associations used for integrative analyses were mainly from populations of European ancestry, resulting in potential missing of pivotal biological insights in other continental populations due to population heterogeneity. Here we conducted TWAS and SMR integrative analyses using blood eQTL (from 162 subjects) and GWAS data (22 778 cases and 35 362 controls) of schizophrenia in East Asian (EAS) populations. Both TWAS (P = 2.89 x 10(-14)) and SMR (P = 6.04 x 10(-5)) analyses showed that decreased TMEM180 mRNA expression was significantly associated with risk of schizophrenia. We further found that TMEM180 was significantly down-regulated in the peripheral blood of schizophrenia cases compared with controls (P = 8.63 x 10(-4) in EAS sample), and its expression was also significantly lower in the brain tissues of schizophrenia cases compared with controls (P = 1.87 x 10(-5) in European sample from PsychENCODE). Functional explorations suggested that Tmem180 knockdown affected neurodevelopment, ie, proliferation and differentiation of neural stem cells. RNA sequencing showed that pathways regulated by Tmem180 were significantly enriched in brain development and synaptic transmission. In conclusion, our study provides convergent lines of evidence for the involvement of TMEM180 in schizophrenia, and highlights the potential and importance of resource integration and sharing at this big data era in bio-medical research.

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