Assessment of glucocorticoid-induced enhancer activity of eSNP regions using STARR-seq reveals novel molecular mechanisms in psychiatric disorders
Abstract Exposure to stressful events increases risk for psychiatric disorders. Mechanistic insight into genetic factors moderating the impact of stress can increase our understanding of disease processes. Here, we test 3662 SNPs from preselected expression quantitative trait loci in massively parallel reporter assays to identify genetic variants that modulate the activity of regulatory elements sensitive to glucocorticoids, important mediators of the stress response. Of the tested SNP sequences, 547 were located in glucocorticoid-responsive regulatory elements of which 233 showed allele-dependent activity. Transcripts regulated by these variants were enriched for those differentially expressed in psychiatric disorders in postmortem brain. Phenome-wide Mendelian randomization analysis in 4,439 phenotypes revealed potentially causal associations specifically in neuro-behavioral traits, including psychiatric disorders. Finally, functional gene scores derived from these variants were significantly associated with differences in physiological stress measures, suggesting that these may alter disease risk by moderating the individual set point of the stress response..
Medienart: |
Preprint |
---|
Erscheinungsjahr: |
2022 |
---|---|
Erschienen: |
2022 |
Enthalten in: |
bioRxiv.org - (2022) vom: 23. Mai Zur Gesamtaufnahme - year:2022 |
---|
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Penner-Goeke, Signe [VerfasserIn] |
---|
Links: |
Volltext [kostenfrei] |
---|
doi: |
10.1101/2022.05.18.22275090 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
XBI036081728 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | XBI036081728 | ||
003 | DE-627 | ||
005 | 20230429081141.0 | ||
007 | cr uuu---uuuuu | ||
008 | 220525s2022 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1101/2022.05.18.22275090 |2 doi | |
035 | |a (DE-627)XBI036081728 | ||
035 | |a (biorXiv)10.1101/2022.05.18.22275090 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | |a 570 |q DE-84 | |
100 | 1 | |a Penner-Goeke, Signe |e verfasserin |4 aut | |
245 | 1 | 0 | |a Assessment of glucocorticoid-induced enhancer activity of eSNP regions using STARR-seq reveals novel molecular mechanisms in psychiatric disorders |
264 | 1 | |c 2022 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a Computermedien |b c |2 rdamedia | ||
338 | |a Online-Ressource |b cr |2 rdacarrier | ||
520 | |a Abstract Exposure to stressful events increases risk for psychiatric disorders. Mechanistic insight into genetic factors moderating the impact of stress can increase our understanding of disease processes. Here, we test 3662 SNPs from preselected expression quantitative trait loci in massively parallel reporter assays to identify genetic variants that modulate the activity of regulatory elements sensitive to glucocorticoids, important mediators of the stress response. Of the tested SNP sequences, 547 were located in glucocorticoid-responsive regulatory elements of which 233 showed allele-dependent activity. Transcripts regulated by these variants were enriched for those differentially expressed in psychiatric disorders in postmortem brain. Phenome-wide Mendelian randomization analysis in 4,439 phenotypes revealed potentially causal associations specifically in neuro-behavioral traits, including psychiatric disorders. Finally, functional gene scores derived from these variants were significantly associated with differences in physiological stress measures, suggesting that these may alter disease risk by moderating the individual set point of the stress response. | ||
700 | 1 | |a Bothe, Melissa |e verfasserin |4 aut | |
700 | 1 | |a Kappelmann, Nils |e verfasserin |4 aut | |
700 | 1 | |a Kreitmaier, Peter |e verfasserin |4 aut | |
700 | 1 | |a Kaya, Ezgi |e verfasserin |4 aut | |
700 | 1 | |a Pöhlchen, Dorothee |e verfasserin |4 aut | |
700 | 1 | |a Kühnel, Anne |e verfasserin |4 aut | |
700 | 1 | |a Czamara, Darina |e verfasserin |4 aut | |
700 | 1 | |a Glaser, Laura V. |e verfasserin |4 aut | |
700 | 1 | |a Roeh, Simone |e verfasserin |4 aut | |
700 | 1 | |a Ködel, Maik |e verfasserin |4 aut | |
700 | 1 | |a Monteserin-Garcia, Jose |e verfasserin |4 aut | |
700 | 1 | |a Rummel, Christine |e verfasserin |4 aut | |
700 | 1 | |a Arloth-Knauer, Janine |e verfasserin |4 aut | |
700 | 1 | |a Diener-Hölzl, Laura |e verfasserin |4 aut | |
700 | 1 | |a Woelfel, Barbara |e verfasserin |4 aut | |
700 | 1 | |a Sauer, Susann |e verfasserin |4 aut | |
700 | 1 | |a Riesenberg, Stephan |e verfasserin |4 aut | |
700 | 1 | |a Ziller, Michael J. |e verfasserin |4 aut | |
700 | 1 | |a Labeur, Marta |e verfasserin |4 aut | |
700 | 1 | |a Meijsing, Sebastiaan H. |e verfasserin |4 aut | |
700 | 1 | |a Binder, Elisabeth B. |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t bioRxiv.org |g (2022) vom: 23. Mai |
773 | 1 | 8 | |g year:2022 |g day:23 |g month:05 |
856 | 4 | 0 | |u http://dx.doi.org/10.1101/2022.05.18.22275090 |z kostenfrei |3 Volltext |
912 | |a GBV_XBI | ||
912 | |a SSG-OLC-PHA | ||
951 | |a AR | ||
952 | |j 2022 |b 23 |c 05 | ||
953 | |2 045F |a 570 |