Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.10.25.761398

Loss of PEA-15 Alters ERK/MAPK Signaling and Circadian Function in the Suprachiasmatic Nucleus

Abstract

Circadian rhythms are a fundamental biological process that coordinates physiological functions, behavior, and metabolism with an approximately 24-hour periodicity. At the center of the mammalian circadian timing system is the suprachiasmatic nucleus (SCN) of the hypothalamus, which generates robust, clock-gated neuronal output that establishes the temporal organization of cellular and physiological processes throughout the body. Our previous work demonstrated that the scaffold protein PEA-15 (phosphoprotein enriched in astrocytes 15) is highly expressed in the SCN and dynamically interacts with ERK, a key effector kinase of the MAPK pathway, to regulate its subcellular localization. Given the important role of ERK/MAPK signaling in circadian timing and photic entrainment, we extended this work using PEA-15 knockout (PEA-15-/-) mice to determine how loss of PEA-15 affects circadian timing, entrainment, and ERK signaling within the SCN. At the cellular level, both clock-gated and light-evoked ERK activation were significantly reduced in PEA-15-/- mice compared with wild-type controls. Under constant darkness, PEA-15-/- mice exhibited a significantly shorter free-running period and reduced locomotor activity relative to wild-type animals. Assessment of circadian entrainment using jet-lag resetting and Aschoff type I light-pulse paradigms revealed a blunted phase-delay response to light and an accelerated rate of entrainment to a phase-advancing light stimulus. Thus, loss of PEA-15 alters multiple properties of the SCN clock, including its intrinsic period and its responsiveness to photic input, with effects that depend on the direction of phase resetting. Collectively, these findings identify PEA-15 as an important regulator of SCN circadian function and implicate ERK/MAPK signaling as one mechanism through which PEA-15 modulates clock timing and photic entrainment.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Wheaton, K., Halloy, N., Formanowicz, M., Ramos, J. W., Hoyt, K. R., Obrietan, K.. 2026-10-27. Loss of PEA-15 Alters ERK/MAPK Signaling and Circadian Function in the Suprachiasmatic Nucleus. https://doi.org/10.64898/2026.10.25.761398

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

KEEP EXPLORING

Related preprints

Brain representations of visual short-term memories during healthy human aging: occipital decline and frontoparietal compensation

Visual short-term memory declines steeply with age, but the link to neural representations of memory content remains unknown. We used fMRI decoding to relate remembered motion-direction representations in visual and frontoparietal cortex to age and performance, in 115 adults, aged 25-87, from the Cambridge Centre for Ageing and Neuroscience (Cam-CAN) cohort. Decoding was strongest in visual cortex, but also significant in frontoparietal regions, with different profiles. Visual representations weakened with memory load and age, and statistically mediated age-related performance decline, especially during recall. This coupling, however, weakened with age: some older adults retained stronger visual representations than performance implied, suggesting impaired access to a partially preserved memory trace. Frontoparietal representations, instead, were largely insensitive to load and strengthened with age during maintenance, partially offsetting performance decline. Therefore, interventions to boost VSTM in older adults might target compensatory frontoparietal representations during memory maintenance, and readout of untapped visual representations at recall.

neuroscience↗

Lexical surprisal drives pupil dilation during continuous story listening

The pupil famously adjusts its dilation in response to light, but its role extends far beyond this basic sensory function. Its fluctuations index arousal and mental effort, beyond luminance-related dynamics, making it a sensitive marker of internal cognitive states. A growing body of work shows that these pupil-linked signals extend beyond the visual domain. However, which processes drive pupil responses in more naturalistic settings remains unclear as most evidence comes from tightly controlled paradigms that strip away the richness of real-world experience. Language offers a uniquely powerful window into this question, as it can allow us to create rich paradigms without having any visual, i.e. luminance, confounds. Moreover, language comprehension hinges on continuous prediction: listeners constantly generate expectations about upcoming input, and the discrepancy between expectation and actual input - contextual prediction error, or surprisal - carries measurable cognitive costs. Here, we tested the hypothesis that pupil-linked arousal indexes these linguistic surprisal signals during naturalistic listening. We recorded pupil responses while volunteers listened to naturalistic spoken stories in darkness, which were either intact or reversed. Reversed speech preserves the acoustics of the signal while destroying its intelligibility. Pupil dilation selectively tracked lexical surprisal within a late window of 1,700 to 2,350 milliseconds following word onset, in forward, but not control, backward speech. These findings indicate that pupil-linked arousal is tuned to global, context-dependent processing, tracking the cognitive cost of updating a predictive model during naturalistic listening.

neuroscience↗

Disrupting SORL1-retromer endosomal recycling in mice drives the age-dependent neurodegenerative signature of Alzheimer's disease

MRI studies have mapped the atrophic signature that distinguishes Alzheimer's disease (AD), isolating regions differentially vulnerable to its age-dependent neurodegenerative process. We test the hypothesis that an endosomal recycling pathway regulated by the interaction of SORL1 with retromer, which is pathogenically disrupted in AD, might drive the neurodegenerative process via multiple yearlong studies in over 140 wildtype and SORL1 deficient mice, modeling AD's causative mutations. MRI studies revealed that SORL1 deficiency induced an age-dependent AD-pattern of atrophy, centered on the trans-entorhinal cortex, and that atrophy was prevented by SORL1 restoration, secondary to overexpressing the retromer protein VPS26b. Postmortem studies validated that the atrophy reflects neuronal loss. Proteomic profiling revealed that the atrophy is associated with reductions in cell death suppressors, one of which was then found deficient in the trans-entorhinal cortex of AD patients. Besides supporting the hypothesis, taken together with other findings, the results suggest that SORL1-retromer disruptions represent a therapeutically-amenable common 'neurodegeneration pathway' in AD.

neuroscience↗