Sunday, December 23, 2018

Biological Processes Modulating Longevity across Primates: A Phylogenetic Genome-Phenome Analysis

Biological Processes Modulating Longevity across Primates: A Phylogenetic Genome-Phenome Analysis. Gerard MuntanĂ© et al. Molecular Biology and Evolution, Volume 35, Issue 8, 1 August 2018, Pages 1990–2004, https://doi.org/10.1093/molbev/msy105

Abstract: Aging is a complex process affecting different species and individuals in different ways. Comparing genetic variation across species with their aging phenotypes will help understanding the molecular basis of aging and longevity. Although most studies on aging have so far focused on short-lived model organisms, recent comparisons of genomic, transcriptomic, and metabolomic data across lineages with different lifespans are unveiling molecular signatures associated with longevity. Here, we examine the relationship between genomic variation and maximum lifespan across primate species. We used two different approaches. First, we searched for parallel amino-acid mutations that co-occur with increases in longevity across the primate linage. Twenty-five such amino-acid variants were identified, several of which have been previously reported by studies with different experimental setups and in different model organisms. The genes harboring these mutations are mainly enriched in functional categories such as wound healing, blood coagulation, and cardiovascular disorders. We demonstrate that these pathways are highly enriched for pleiotropic effects, as predicted by the antagonistic pleiotropy theory of aging. A second approach was focused on changes in rates of protein evolution across the primate phylogeny. Using the phylogenetic generalized least squares, we show that some genes exhibit strong correlations between their evolutionary rates and longevity-associated traits. These include genes in the Sphingosine 1-phosphate pathway, PI3K signaling, and the Thrombin/protease-activated receptor pathway, among other cardiovascular processes. Together, these results shed light into human senescence patterns and underscore the power of comparative genomics to identify pathways related to aging and longevity.

Keywords: evolution, longevity, primates, genotype-phenotype, aging

Kay and Ross (2003) priming findings not replicable, despite counting on higher power

Testing the effect of cooperative/competitive priming on the Prisoner’s Dilemma. A replication study. Anabel Belaus, Cecilia Reyna, Esteban Freidin. PLOS, Dec 20, https://doi.org/10.1371/journal.pone.0209263

Abstract: The replicability crisis in psychology demands direct replications to test the reliability of relevant phenomena. Prime-to-behavior effects have been an area under intense scrutiny given its surprising results. However, intuitive unsurprising effects have been mostly neglected, while they may lack robustness as well. In the present study, we focused on an intuitive prime-to-behavior effect in which Kay and Ross (2003) used a 2x2 design to test cooperation/competition priming crossed with an explicit/non-explicit construal of a Prisoner’s Dilemma (PD). They found a stronger assimilation effect of priming when the situational construal anteceded the decision, but we could not reproduce their findings in the present close replication, despite counting on higher power. Even with limitations due to the unavailability of original materials, this replication presents evidence that questions the existence of the original finding, and highlights the need for further replications to get a deeper understanding of the hypothesized effect. The complete project is available at: https://osf.io/dhfns/.