TY - JOUR AB - The execution of cognitive functions requires coordinated circuit activity across different brain areas that involves the associated firing of neuronal assemblies. Here, we tested the circuit mechanism behind assembly interactions between the hippocampus and the medial prefrontal cortex (mPFC) of adult rats by recording neuronal populations during a rule-switching task. We identified functionally coupled CA1-mPFC cells that synchronized their activity beyond that expected from common spatial coding or oscillatory firing. When such cell pairs fired together, the mPFC cell strongly phase locked to CA1 theta oscillations and maintained consistent theta firing phases, independent of the theta timing of their CA1 counterpart. These functionally connected CA1-mPFC cells formed interconnected assemblies. While firing together with their CA1 assembly partners, mPFC cells fired along specific theta sequences. Our results suggest that upregulated theta oscillatory firing of mPFC cells can signal transient interactions with specific CA1 assemblies, thus enabling distributed computations. AU - Nardin, Michele AU - Käfer, Karola AU - Stella, Federico AU - Csicsvari, Jozsef L ID - 14314 IS - 9 JF - Cell Reports TI - Theta oscillations as a substrate for medial prefrontal-hippocampal assembly interactions VL - 42 ER - TY - JOUR AB - Cytosine methylation within CG dinucleotides (mCG) can be epigenetically inherited over many generations. Such inheritance is thought to be mediated by a semiconservative mechanism that produces binary present/absent methylation patterns. However, we show here that in Arabidopsis thaliana h1ddm1 mutants, intermediate heterochromatic mCG is stably inherited across many generations and is quantitatively associated with transposon expression. We develop a mathematical model that estimates the rates of semiconservative maintenance failure and de novo methylation at each transposon, demonstrating that mCG can be stably inherited at any level via a dynamic balance of these activities. We find that DRM2 – the core methyltransferase of the RNA-directed DNA methylation pathway – catalyzes most of the heterochromatic de novo mCG, with de novo rates orders of magnitude higher than previously thought, whereas chromomethylases make smaller contributions. Our results demonstrate that stable epigenetic inheritance of mCG in plant heterochromatin is enabled by extensive de novo methylation. AU - Lyons, David B. AU - Briffa, Amy AU - He, Shengbo AU - Choi, Jaemyung AU - Hollwey, Elizabeth AU - Colicchio, Jack AU - Anderson, Ian AU - Feng, Xiaoqi AU - Howard, Martin AU - Zilberman, Daniel ID - 12672 IS - 3 JF - Cell Reports TI - Extensive de novo activity stabilizes epigenetic inheritance of CG methylation in Arabidopsis transposons VL - 42 ER - TY - JOUR AB - Alpha oscillations are a distinctive feature of the awake resting state of the human brain. However, their functional role in resting-state neuronal dynamics remains poorly understood. Here we show that, during resting wakefulness, alpha oscillations drive an alternation of attenuation and amplification bouts in neural activity. Our analysis indicates that inhibition is activated in pulses that last for a single alpha cycle and gradually suppress neural activity, while excitation is successively enhanced over a few alpha cycles to amplify neural activity. Furthermore, we show that long-term alpha amplitude fluctuations—the “waxing and waning” phenomenon—are an attenuation-amplification mechanism described by a power-law decay of the activity rate in the “waning” phase. Importantly, we do not observe such dynamics during non-rapid eye movement (NREM) sleep with marginal alpha oscillations. The results suggest that alpha oscillations modulate neural activity not only through pulses of inhibition (pulsed inhibition hypothesis) but also by timely enhancement of excitation (or disinhibition). AU - Lombardi, Fabrizio AU - Herrmann, Hans J. AU - Parrino, Liborio AU - Plenz, Dietmar AU - Scarpetta, Silvia AU - Vaudano, Anna Elisabetta AU - De Arcangelis, Lucilla AU - Shriki, Oren ID - 14402 IS - 10 JF - Cell Reports TI - Beyond pulsed inhibition: Alpha oscillations modulate attenuation and amplification of neural activity in the awake resting state VL - 42 ER - TY - JOUR AB - Dravet syndrome is a neurodevelopmental disorder characterized by epilepsy, intellectual disability, and sudden death due to pathogenic variants in SCN1A with loss of function of the sodium channel subunit Nav1.1. Nav1.1-expressing parvalbumin GABAergic interneurons (PV-INs) from young Scn1a+/− mice show impaired action potential generation. An approach assessing PV-IN function in the same mice at two time points shows impaired spike generation in all Scn1a+/− mice at postnatal days (P) 16–21, whether deceased prior or surviving to P35, with normalization by P35 in surviving mice. However, PV-IN synaptic transmission is dysfunctional in young Scn1a+/− mice that did not survive and in Scn1a+/− mice ≥ P35. Modeling confirms that PV-IN axonal propagation is more sensitive to decreased sodium conductance than spike generation. These results demonstrate dynamic dysfunction in Dravet syndrome: combined abnormalities of PV-IN spike generation and propagation drives early disease severity, while ongoing dysfunction of synaptic transmission contributes to chronic pathology. AU - Kaneko, Keisuke AU - Currin, Christopher AU - Goff, Kevin M. AU - Wengert, Eric R. AU - Somarowthu, Ala AU - Vogels, Tim P AU - Goldberg, Ethan M. ID - 11143 IS - 13 JF - Cell Reports TI - Developmentally regulated impairment of parvalbumin interneuron synaptic transmission in an experimental model of Dravet syndrome VL - 38 ER -