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Sherrard, R.

Publications and source records attributed to Sherrard, R..

2 recordsLinked to original sources

Oscillatory impact of Transcranial Magnetic Stimulation at very weak-intensity on the primary motor cortex: A TMS-EEG study in the human brain

Transcranial Magnetic Stimulation is widely used to probe and modulate human brain function, yet the neural effects of stimulation delivered at very low intensities remain unclear. Here, we show that very low intensity magnetic pulses can alter ongoing oscillatory activity in the human primary motor cortex. In healthy participants, we combined transcranial magnetic stimulation with electroencephalography to assess neural responses to single pulses and rhythmic stimulation in the motor cortex. Conventional high intensity stimulation produced robust evoked responses and synchronized beta-frequency oscillations. Low-intensity rhythmic stimulation, despite generating much weaker direct responses, modified local oscillatory activity in a manner consistent with phase-dependent enhancement of ongoing rhythms. These findings suggest that cortical oscillations can be influenced by magnetic fields substantially weaker than those typically used in human studies. Low-intensity stimulation may therefore offer a route towards portable, energy-efficient technologies for investigating and modulating brain networks.

neuroscience↗

The replicative helicase CMG is required for the divergence of cell fates during asymmetric cell division in vivo

The mechanisms that enable differential gene expression in daughter cells produced by asymmetric cell divisions are not well understood. We discovered that the eukaryotic replicative helicase CMG (Cdc45-MCM-GINS) is required for this process in C. elegans. During C. elegans development, some dividing cells give rise to a daughter that survives and a daughter that dies. We found that PSF-2 GINS2, a component of C. elegans CMG, is necessary for the transcriptional burst of the pro-apoptotic gene egl-1 BH3-only, which occurs in the daughter that dies immediately following mother cell division. We present evidence that this requirement is independent of the function of CMG in DNA unwinding. We propose that the recently described histone chaperone activity of CMG causes epigenetic changes at the egl-1 locus during replication in mother cells, and that these changes are required for the increase in egl-1 transcription in the daughter that dies. We also find that PSF-2 is required for the divergence of other cell fates during C. elegans development, suggesting that this function is not restricted to the regulation of egl-1 expression. Our work uncovers a new and unexpected role of CMG in cell fate and a novel intrinsic mechanism for gene expression plasticity in the context of asymmetric cell division.

cell biology↗