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Miller, B. R.

Publications and source records attributed to Miller, B. R..

2 recordsLinked to original sources

Methyl-Metabolite Depletion Elicits Adaptive Responses to Support Heterochromatin Stability and Epigenetic Persistence

S-adenosylmethionine (SAM) is the methyl-donor substrate for DNA and histone methyltransferases that regulate cellular epigenetic states. This metabolism-epigenome link enables the sensitization of chromatin methylation to altered SAM abundance. However, a chromatin-wide understanding of the adaptive/responsive mechanisms that allow cells to actively protect epigenetic information during life-experienced fluctuations in SAM availability are unknown. We identified a robust response to SAM depletion that is highlighted by preferential cytoplasmic and nuclear de novo mono-methylation of H3 Lys 9 (H3K9) at the expense of global losses in histone di- and tri-methylation. Under SAM-depleted conditions, de novo H3K9 mono-methylation preserves heterochromatin stability and supports global epigenetic persistence upon metabolic recovery. This unique chromatin response was robust across the mouse lifespan and correlated with improved metabolic health, supporting a significant role for epigenetic adaptation to SAM depletion in vivo. Together, these studies provide the first evidence for active epigenetic adaptation and persistence to metabolic stress.

biochemistry

An increase in spontaneous activity mediates visual habituation

The cerebral cortex is spontaneously active1,2, but the function of this ongoing activity remains unclear3, 4. One possibility is that spontaneous activity provides contextual information in cortical computations, replaying previously learned patterns of activity5-8 that conditions the cortex to respond more efficiently, based on past experience. To test this, we measured the response of neuronal populations in mouse primary visual cortex with chronic two-photon calcium imaging during a visual habituation to a specific oriented stimulus. We unexpectedly found that, during habituation, spontaneous activity increased in neurons across the full range of orientation selectivity, eventually matching that of evoked levels. The increase in spontaneous activity strongly correlated with the degree of habituation. In fact, boosting spontaneous activity with two-photon optogenetic stimulation to the levels of stimulus-evoked activity induced habituation in naive animals. Our study shows that cortical spontaneous activity is causally linked to habituation, which unfolds by minimizing the difference between spontaneous and stimulus-evoked activity levels, rendering the cortex less responsive. We also show how manipulating spontaneous activity can accelerate this type of learning. We hypothesize that spontaneous activity in visual cortex gates incoming sensory information.

neuroscience