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Costello, R.

Publications and source records attributed to Costello, R..

3 recordsLinked to original sources

Hunger modulates behavioral responses to olfactory and chemotactile cues in the specialist predator of dangerous prey, Berghia stephanieae

Animals continuously evaluate environmental cues to guide approach-avoidance decisions, with internal states like hunger dynamically shaping how stimuli are acted upon. While most studies examine the valence-switching of stimuli from appetitive to aversive using simplified or ambiguous stimuli, we leveraged a system in which a single prey contains both appetitive and aversive features. The nudibranch Berghia stephanieae, is a specialist predator of the sea anemone, Exaiptasia diaphana. These nudibranchs must resolve conflicting signals where chemical cues signal food, while contact can result in injury or death. The danger posed by Exaiptasia was described and quantified through direct counts of nematocysts fired into Berghia and multiple instances where the Berghia was captured and consumed by its prey. To test how internal state influenced the perception of stimuli from prey we recorded predatory behavior of Berghia after different periods of food deprivation. We found that the olfactory cues from prey were attractive to Berghia, even when animals were sated, and usually led to a contact-mediated investigation of prey. Hunger independently modulated olfactory and contact cue valence at different internal states and time scales of food deprivation. Hunger specifically altered the threshold for avoidance following contact with prey, indicating that somatosensory and chemotactile cues are modulated by hunger unlike olfactory cues. Our results highlight how internal state and sensory modality interact to shape decision making in a biologically relevant, high-risk predation context.

animal behavior and cognition↗

Autocrine Signaling by Receptor Tyrosine Kinases in Urothelial Carcinoma of the Bladder

Comprehensive characterizations of bladder cancer (BCa) have established molecular phenotype classes with distinct alterations and survival trends. Extending these studies within the tyrosine kinase (TK) family to identify disease drivers could improve our use of TK inhibitors to treat specific patient groups or individuals. We examined the expression distribution of TKs as a class (n = 89) in The Cancer Genome Atlas (TCGA) muscle invasive BCa data set (n >400). Patient profiles of potentially oncogenic alterations (overexpression and/or amplification) clustered TKs into 3 groups; alterations of group 1 and 3 TKs were associated with significantly worse patient survival relative to those without alterations. Many TK pathways induce epithelial-to-mesenchymal transition (EMT), which promotes tumor invasiveness and metastasis. Overexpression and/or amplification among 9 EMT transcriptional activators occurred in 43% of TCGA cases. Co-occurring alterations of TKs and EMT transcriptional activators involved most group 1 TKs; 24% of these events were associated with significantly worse patient survival. Co-occurring alterations of receptor TKs and their cognate ligands occurred in 16% of TCGA cases and several BCa-derived cell lines. Suppression of GAS6, MST1 or CSF1, or their respective receptors (AXL, MST1R and CSF1R), in BCa cell lines was associated with decreased receptor activation, cell migration, cell proliferation and anchorage independent cell growth. These studies reveal the patterns and prevalence of potentially oncogenic TK pathway-related alterations in BCa and identify specific alterations associated with reduced BCa patient survival. Detection of these features in BCa patients could better inform TK inhibitor use and improve clinical outcomes.

cancer biology↗

Gene duplication accelerates the pace of protein gain and loss from plant organelles.

Introductory paragraphA hallmark of eukaryotic cells is the compartmentalisation of intracellular processes into specialised membrane-bound compartments known as organelles. Plant cells contain several such organelles including the nucleus, chloroplast, mitochondrion, peroxisome, golgi, endoplasmic reticulum and vacuole. Organelle biogenesis and function is dependent on the concerted action of numerous nuclear-encoded proteins which must be imported from the cytosol (or endoplasmic reticulum) where they are made. Using phylogenomic approaches coupled to ancestral state estimation we show that the rate of change in plant organellar proteome content is proportional to the rate of molecular sequence evolution such that the proteomes of chloroplasts and mitochondria lose or gain ~3.2 proteins per million years. We show that these changes in protein targeting have predominantly occurred in genes with regulatory rather than metabolic functions, and thus altered regulatory capacity rather than metabolic function has been the major theme of plant organellar evolution. Finally we show gain and loss of protein targeting occurs at a higher rate following gene duplication events, revealing that gene and genome duplication are a key facilitator of organelle evolution.

evolutionary biology↗