Interacting selection diversifies warning signals in a polytypic frog: an examination with the strawberry poison frog

Abstract Aposematic signals represent one of the most accessible traits to evaluate the interaction of natural and sexual selection on signal evolution. Here we investigate the contributions of these two selective forces on the aposematic signal evolution of the highly polytypic strawberry poison frog, Oophaga pumilio, of Bocas del Toro, Panama. Previous research has shown that the brightness of O. pumilio warning coloration can inform predators of the toxicity levels associated with different populations of the archipelago. Other studies suggest that sexual selection may be influencing warning signal brightness within populations via female mate choice (Isla Solarte, Isla Bastimentos, and Aquacate Peninsula populations) and male-male competition (Isla Solarte). Here we present two non-exclusive scenarios for how natural and sexual selection interact to drive phenotypic variation across this archipelago: (1) predators impose a selective regime whereby populations above a toxicity-brightness threshold are at liberty to diversify via sexual selection and below which populations are constrained to maintain a stricter resemblance to a more cryptic population mean, and (2) synergistic/additive effects of inter-and intrasexual selection drive the evolution of brighter males within populations above this toxicity threshold. We investigate whether aposematic patterns of divergence across the archipelago relative to the common mainland phenotype meet these predictions using existing data on O. pumilio morph toxicity measures and overall conspicuousness estimates to an avian predator. Using standardized z-scores to evaluate the range of trait values, we find that indeed the population representative of the common mainland phenotype (Almirante) represents an intermediate level of both toxicity and conspicuousness, and that derived Bocas del Toro populations vary in each of those components in directions predicted by the proposed scenarios. Furthermore, we find greater divergence towards conspicuousness than crypsis, 123 Evol Ecol (2013) 27:693-710 DOI 10.1007 a pattern suggestive of sexual and natural selection acting synergistically in morphs with high toxicity

Expression profiling of circulating tumor cells in metastatic breast cancer.

Circulating tumor cells (CTCs) are prognostic in all stages of breast cancer. However, since they are extremely rare, little is known about the molecular nature of these cells. We report a novel strategy for the isolation and expression profiling of pure populations of CTCs derived from peripheral blood. We developed a method to isolate CTCs based on immunomagnetic capture followed by fluorescence-activated cell sorting (IE/FACS). After assay validation using the BT474 cell line spiked into blood samples in vitro, RNA from CTCs isolated from the blood of five metastatic breast cancer (MBC) patients was linearly amplified and subjected to gene expression profiling via cDNA microarrays. We isolated a range of 9-993 captured CTCs from five MBC patients' blood and profiled their RNA in comparison to a diverse panel of primary breast tumors (n = 55). Unsupervised hierarchical clustering revealed that CTC profiles clustered with more aggressive subtypes of primary breast tumors and were readily distinguishable from peripheral blood (PB) and normal epithelium. Differential expression analysis revealed CTCs to have downregulated apoptosis, and they were distinguishable from PB by the relative absence of immune-related signals. As expected, CTCs from MBC had significantly higher risk of recurrence scores than primary tumors (p = 0.0073). This study demonstrates that it is feasible to isolate CTCs from PB with high purity through IE/FACS and profile them via gene expression analysis. Our approach may inform the discovery of therapeutic predictors and be useful for real-time identification of emerging resistance mechanisms in MBC patients