Significance Snake venoms are toxic protein cocktails used for prey capture. To investigate the evolution of these complex biological weapon systems, we sequenced the genome of a venomous snake, the king cobra, and assessed the composition of venom gland expressed genes, small RNAs, and secreted venom proteins. We show that regulatory components of the venom secretory system may have evolved from a pancreatic origin and that venom toxin genes were co-opted by distinct genomic mechanisms. After co-option, toxin genes important for prey capture have massively expanded by gene duplication and evolved under positive selection, resulting in protein neofunctionalization. This diverse and dramatic venom-related genomic response seemingly occurs in response to a coevolutionary arms race between venomous snakes and their prey.

Frontal contributions to cognitive decline in aging were explored using functional MRI. Frontal regions active in younger adults during self-initiated (intentional) memory encoding were under-recruited in older adults. Older adults showed less activity in anterior-ventral regions associated with controlled use of semantic information. Under-recruitment was reversed by requiring semantic elaboration suggesting it stemmed from difficulty in spontaneous recruitment of available frontal resources. In addition, older adults recruited multiple frontal regions in a nonselective manner for both verbal and nonverbal materials. Lack of selectivity was not reversed during semantically directed encoding even when under-recruitment was diminished. These findings suggest two separate forms of age-associated change in frontal cortex: under-recruitment and nonselective recruitment. The former is reversible and potentially amenable to cognitive training; the latter may reflect a less malleable change associated with cognitive decline in advanced aging.

Memory for the experiences of one's life, autobiographical memory (AM), is one of the most human types of memory, yet comparatively little is known of its neurobiology. A positron emission tomography (PET) study of AM retrieval revealed that the left frontal cortex was significantly active during retrieval (compared to memory control tasks), together with activation in the inferior temporal and occipital lobes in the left hemisphere. We propose that this left frontal lobe activation reflects the operation of control processes that modulate the construction of AMs in posterior neocortical networks.

The authors examined the degree to which aging and Alzheimer's disease (AD) influence the ability to control attention when conflict is presented in terms of incongruent mapping between a stimulus and the appropriate response. In a variant of the Simon task, healthy older adults and older adults with mild or very mild AD showed disproportionately larger reaction time (RT) costs when the stimulus and response were in conflict relative to RT costs of healthy younger adults. Analyses of RT distributions provide support for a 2-process model of the Simon effect in which there is a short-lived transient effect of the irrelevant dimension in younger adults and a more sustained influence across the RT distribution in older adults. An analysis of error rates showed that the older adults with mild and very mild AD made more errors on incongruent trials, suggesting that AD leads to increased likelihood of selecting the prepotent pathway. The findings are discussed in terms of the special nature of the response requirements of the Simon task to better illuminate the attentional decrements in both healthy aging and early stage AD.

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