bioRxiv ScienceSearch

bioRxiv · 10.1101/044917

The Opposing Effects of Hedonic and Eudaimonic Happiness on Gene Expression is Correlated Noise

Abstract

BackgroundThis paper presents a re-analysis of the gene set data from Fredrickson et al. 2013 and Fredrickson et al. 2015 which purportedly showed opposing effects of hedonic and eudaimonic happiness on the expression levels of a set of genes that have been correlated with social adversity. Fredrickson et al. 2015 used a linear model of fixed effects with correlated error (using GLS) to estimate the partial regression coefficients.\n\nMethodsThe standardized effects of hedonic and eudaimonic happiness on CTRA gene set expression estimated by GLS was compared to estimates using multivariate (OLS) linear models and generalized estimating equation (GEE) models. The OLS estimates were tested using a bootstrap t-test, OBriens OLS test, a permutation t test, and the rotation z-test. The GEE estimates were tested using a Wald test with robust standard errors. The performance (type I, type II, and type M error) of all tests was investigated using a Monte Carlo simulation of data modeled after the 2015 dataset.\n\nResultsStandardized OLS effects (mean partial regression coefficients) of Hedonia and Eudaimonia on gene expression levels are very small in both the 2013 and 2015 data, as well as the combined data.The p-values from all tests fail to reject any of the null models. The GEE estimates and tests are nearly identical to the OLS estimates and tests. By contrast, the GLS estimates are inconsistent between data sets, but in each dataset, at least one coefficient is large and highly statistically significant. The Monte Carlo simulation of error rates shows inflated type I error from the GLS test on data with a similar correlation structure to that in the 2015 dataset, and this error rate increases as the number of outcomes increases relative to the number of subjects. Bootstrap and permutation GLS distributions suggest that the GLS model not only results in downward biased standard errors but also inflated coefficients. Both distributions also show the expected, strong, negative correlation between the coefficients for Hedonia and Eudaimonia.\n\nDiscussionThe results fail to support opposing effects, or any detectable effect, of hedonic and eudaimonic well being on the pattern of gene expression. The apparently replicated pattern of hedonic and eudaimonic effects on gene expression is most parsimoniously explained as \"correlated noise\" due to the geometry of multiple regression. A linear mixed model for estimating fixed effects in designs with many repeated measures or outcomes should be used cautiously because of the potentially inflated type 1 and type M error.

Explore related subjects

Keep this discovery

BibTeXRIS

Jeffrey A Walker. 2016-03-20. The Opposing Effects of Hedonic and Eudaimonic Happiness on Gene Expression is Correlated Noise. https://doi.org/10.1101/044917

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Rapid evolution of primate type 2 immune response factors linked to asthma susceptibility

Host immunity pathways evolve rapidly in response to antagonism by pathogens. Microbial infections can also trigger excessive inflammation that contributes to diverse autoimmune disorders including asthma, lupus, diabetes, and arthritis. Definitive links between immune system evolution and human autoimmune disease remain unclear. Here we provide evidence that several components of the type 2 immune response pathway have been subject to recurrent positive selection in the primate lineage. Notably, rapid evolution of the central immune regulator IL13 corresponds to a polymorphism linked to asthma susceptibility in humans. We also find evidence of accelerated amino acid substitutions as well as repeated gene gain and loss events among eosinophil granule proteins, which act as toxic antimicrobial effectors that promote asthma pathology by damaging airway tissues. These results support the hypothesis that evolutionary conflicts with pathogens promote tradeoffs for increasingly robust immune responses during animal evolution. Our findings are also consistent with the view that natural selection has contributed to the spread of autoimmune disease alleles in humans.

Genetics

Single Cell Expression Data Reveal Human Genes that Escape X-Chromosome Inactivation

Sex chromosomes pose an inherent genetic imbalance between genders. In mammals, one of the females X-chromosomes undergoes inactivation (Xi). Indirect measurements estimate that about 20% of Xi genes completely or partially escape inactivation. The identity of these escapee genes and their propensity to escape inactivation remain unsolved. A direct method for identifying escapees was applied by quantifying differential allelic expression from single cells. RNA-Seq fragments were assigned to informative SNPs which were labeled by the appropriate parental haplotype. This method was applied for measuring allelic specific expression from Chromosome-X (ChrX) and an autosomal chromosome as a control. We applied the protocol for measuring biallelic expression from ChrX to 104 primary fibroblasts. Out of 215 genes that were considered, only 13 genes (6%) were associated with biallelic expression. The sensitivity of escapees' identification was increased by combining SNP mapping for parental diploid genomes together with RNA-Seq from clonal single cells (25 lymphoblasts). Using complementary protocols, referred to as strict and relaxed, we confidently identified 25 and 31escapee genes, respectively. When pooled versions of 30 and 100 cells were used, <50% of these genes were revealed. We assessed the generality of our protocols in view of an escapee catalog compiled from indirect methods. The overlap between the escapee catalog and the genes list from this study is statistically significant (P-value of E-07). We conclude that single cells expression data are instrumental for studying X-inactivation with an improved sensitivity. Finally, our results support the emerging notion of the non-deterministic nature of genes that escape X-chromosome inactivation.

Genetics

Frequency of mosaicism points towards mutation-prone early cleavage cell divisions.

It has recently become possible to directly estimate the germ-line de novo mutation (dnm) rate by sequencing the whole genome of father-mother-offspring trios, and this has been conducted in human1-5, chimpanzee6, mice7, birds8 and fish9. In these studies dnms are typically defined as variants that are heterozygous in the offspring while being absent in both parents. They are assumed to have occurred in the germ-line of one of the parents and to have been transmitted to the offspring via the sperm cell or oocyte. This definition assumes that detectable mosaicism in the parent in which the mutation occurred is negligible. However, instances of detectable mosaicism or premeiotic clusters are well documented in humans and other organisms, including ruminants10-12. We herein take advantage of cattle pedigrees to show that as much as [~]30% to [~]50% of dnms present in a gamete may occur during the early cleavage cell divisions in males and females, respectively, resulting in frequent detectable mosaicism and a high rate of sharing of multiple dnms between siblings. This should be taken into account to accurately estimate the mutation rate in cattle and other species.

Genetics