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Brown, M. R.

Publications and source records attributed to Brown, M. R..

21 records · Page 2Linked to original sources

Multi-ancestry analysis of gene-sleep interactions in 126,926 individuals identifies multiple novel blood lipid loci that contribute to our understanding of sleep-associated adverse blood lipid profile

Both short and long sleep are associated with an adverse lipid profile, likely through different biological pathways. To provide new insights in the biology of sleep-associated adverse lipid profile, we conducted multi-ancestry genome-wide sleep-SNP interaction analyses on three lipid traits (HDL-c, LDL-c and triglycerides). In the total study sample (discovery + replication) of 126,926 individuals from 5 different ancestry groups, when considering either long or short total sleep time interactions in joint analyses, we identified 49 novel lipid loci, and 10 additional novel lipid loci in a restricted sample of European-ancestry cohorts. In addition, we identified new gene-sleep interactions for known lipid loci such as LPL and PCSK9. The novel gene-sleep interactions had a modest explained variance in lipid levels: most notable, gene-short-sleep interactions explained 4.25% of the variance in triglyceride concentration. Collectively, these findings contribute to our understanding of the biological mechanisms involved in sleep-associated adverse lipid profiles.

genomics↗

Genome-wide association and functional studies identify 46 novel loci for alcohol consumption and suggest common genetic mechanisms with neuropsychiatric disorders

Excessive alcohol consumption is one of the main causes of death and disability worldwide. Alcohol consumption is a heritable complex trait. We conducted a genome-wide association study (GWAS) of alcohol use in ~480,000 people of European descent to decipher the genetic architecture of alcohol intake. We identified 46 novel, common loci, and investigated their potential functional significance using magnetic resonance imaging data, gene expression and behavioral studies in Drosophila. Our results identify new genetic pathways associated with alcohol consumption and suggest common genetic mechanisms with several neuropsychiatric disorders including schizophrenia.

genetics↗

Life history evolution and phenotypic plasticity in parasitic eyebrights (Euphrasia, Orobanchaceae)

Premise of the studyParasite lifetime reproductive success is determined by both genetic variation and phenotypically plastic life history traits that respond to host quality and external environment. Here, we use the generalist parasitic plant genus Euphrasia to investigate life history trait variation, in particular whether there is a trade-off between growth and reproduction, and how life history traits are affected by host quality.\n\nMethodsWe perform a common garden experiment to evaluate life history trait differences between eleven Euphrasia taxa grown on a common host, document phenotypic plasticity when a single Euphrasia species is grown on eight different hosts, and relate our observations to trait differences recorded in the wild.\n\nKey resultsEuphrasia exhibit a range of life history strategies that differ between species that transition rapidly to flower at the expense of early season growth, and those that invest in vegetative growth and delay flowering. Many life history traits show extensive phenotypic plasticity in response to host quality and demonstrate the costs of attaching to a low-quality host.\n\nConclusionsCommon garden experiments reveal trait differences between taxonomically complex Euphrasia species that are characterised by postglacial speciation and hybridisation. Our experiments suggest life history strategies in this generalist parasitic plant genus are the product of natural selection on traits related to growth and flowering. However, host quality may be a primary determinant of lifetime reproductive success.

evolutionary biology↗