Summary: Researchers have identified a number of variable locations in the genome that influence hippocampal gene activity and may contribute to brain disorders.
Source: University of Basel.
New findings will help to identify the genetic causes of brain disorders: researchers at the Universities of Basel, Bonn and Cologne have presented a systematic catalog of specific variable locations in the genome that influence gene activity in the human hippocampus, as they report in the journal Nature Communications.
Individual differences in gene regulation contribute to the development of numerous multifactorial disorders. Researchers are therefore attempting to clarify the influence of genetic variants (single-nucleotide polymorphisms, or SNPs) on gene expression and on the epigenetic modification of regulatory sections of the genome (DNA methylation). The German–Swiss team has now studied the genetic determinants of gene expression, as well as the process of DNA methylation in the human hippocampus.
Three million genomic locations analyzed
The researchers have presented an extensive catalog of variable locations in the genome – that is, of SNPs – that affect the activity of genes in the human hippocampus. Specifically, they have analyzed the influence of more than three million SNPs, spread throughout the genome, on activity in nearby genes and the methylation of adjacent DNA sections.
The special thing about their work is that the researchers used freshly frozen hippocampus tissue obtained during surgery on 110 treatment-resistant epilepsy patients. They extracted DNA and RNA from the hippocampus tissue and, for all of the obtained samples, used microchips to determine several hundred thousand SNPs, as well as the degree of methylation at several hundred thousand locations (known as CpG dinucleotides) in the genome. Among other analyses, they measured the gene expression of over 15,000 genes using RNA microchips.
Development of schizophrenia
The researchers also demonstrated the preferred areas in which variably methylated CpG dinucleotides appear in the genome, and they were able to assign these to specific regulatory elements, revealing a link to brain disorders: a significant proportion of the identified SNPs that individually influence DNA methylation and gene expression in the hippocampus also contribute to the development of schizophrenia. This underlines the potentially significant role played by SNPs with a regulatory effect in the development of brain disorders.
The study’s findings will make it considerably easier to interpret evidence of genetic associations with brain disorders in the future. Of the SNPs involved in the development of brain disorders, many of those identified in recent years are located in the non-coding part of the genome. Their functional effect in cells is therefore largely unclear.
About this neuroscience research article
Funding: An important factor in the project’s success was the close cooperation between the Universities of Basel, Bonn and Cologne. This collaboration is supported by the IntegraMent Consortium, which is sponsored by Germany’s Federal Ministry of Education and Research and coordinated by Professor Markus Nöthen of the University of Bonn.
Source: Sven Cichon – University of Basel
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Full open access research for “Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus” by Herbert Schulz, Ann-Kathrin Ruppert, Stefan Herms, Christiane Wolf, Nazanin Mirza-Schreiber, Oliver Stegle, Darina Czamara, Andreas J. Forstner, Sugirthan Sivalingam, Susanne Schoch, Susanne Moebus, Benno Pütz, Axel Hillmer, Nadine Fricker, Hartmut Vatter, Bertram Müller-Myhsok, Markus M. Nöthen, Albert J. Becker, Per Hoffmann, Thomas Sander & Sven Cichon in Nature Communications. Published online November 15 2017 doi:10.1038/s41467-017-01818-4
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University of Basel “Tracking Down Genetic Influences on Brain Disorders.” NeuroscienceNews. NeuroscienceNews, 27 November 2017.
University of Basel (2017, November 27). Tracking Down Genetic Influences on Brain Disorders. NeuroscienceNews. Retrieved November 27, 2017 from http://neurosciencenews.com/genetics-brain-disorders-8036/
University of Basel “Tracking Down Genetic Influences on Brain Disorders.” http://neurosciencenews.com/genetics-brain-disorders-8036/ (accessed November 27, 2017).
Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus
Emerging evidence emphasizes the strong impact of regulatory genomic elements in neurodevelopmental processes and the complex pathways of brain disorders. The present genome-wide quantitative trait loci analyses explore the cis-regulatory effects of single-nucleotide polymorphisms (SNPs) on DNA methylation (meQTL) and gene expression (eQTL) in 110 human hippocampal biopsies. We identify cis-meQTLs at 14,118 CpG methylation sites and cis-eQTLs for 302 3′-mRNA transcripts of 288 genes. Hippocampal cis-meQTL-CpGs are enriched in flanking regions of active promoters, CpG island shores, binding sites of the transcription factor CTCF and brain eQTLs. Cis-acting SNPs of hippocampal meQTLs and eQTLs significantly overlap schizophrenia-associated SNPs. Correlations of CpG methylation and RNA expression are found for 34 genes. Our comprehensive maps of cis-acting hippocampal meQTLs and eQTLs provide a link between disease-associated SNPs and the regulatory genome that will improve the functional interpretation of non-coding genetic variants in the molecular genetic dissection of brain disorders.
“Genome-wide mapping of genetic determinants influencing DNA methylation and gene expression in human hippocampus” by Herbert Schulz, Ann-Kathrin Ruppert, Stefan Herms, Christiane Wolf, Nazanin Mirza-Schreiber, Oliver Stegle, Darina Czamara, Andreas J. Forstner, Sugirthan Sivalingam, Susanne Schoch, Susanne Moebus, Benno Pütz, Axel Hillmer, Nadine Fricker, Hartmut Vatter, Bertram Müller-Myhsok, Markus M. Nöthen, Albert J. Becker, Per Hoffmann, Thomas Sander & Sven Cichon in Nature Communications. Published online November 15 2017 doi:10.1038/s41467-017-01818-4
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