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Weaver, K. E.

Publications and source records attributed to Weaver, K. E..

2 recordsLinked to original sources

Developmental relationships between the human alpha rhythm and intrinsic neural timescales are dependent on neural hierarchy

Maturation of human brain structure has been well-studied, but developmental changes to brain physiology are not as well understood. One consistent finding is that the peak alpha rhythm frequency (PAF) increases throughout childhood. Another is that resting-state functional connectivity shifts from sensorimotor regions in children to association regions in adolescents, a reorganization along a hierarchy called the sensorimotor-to-association (S-A) axis. In mature brains, the S-A axis has been parcellated physiologically using the duration of persistent neural activity, known as the intrinsic neural timescale (INT), which increases along the hierarchy. Here we studied the development of PAF and INT in a cohort of epilepsy patients 3 - 33 years of age undergoing intracranial electrocorticographic (ECoG) monitoring. Given the well-known developmental trajectory of PAF, and the ability to delineate hierarchy using INT, we hypothesized that changes to PAF and INT would correlate across development, but that their relationship may be influenced by hierarchy. Consequently, we predicted that age-dependent PAF increases would accompany INT decreases, and we tested whether their relationship varied between sensorimotor and association regions. We found that PAF increased significantly with age in both sensorimotor and association regions, while age-dependent INT decreases were only significant in association regions. Supporting this finding, we found a strong negative relationship between PAF and INT that was specific to association regions. Together, our results suggest that developmental divisions across the S-A axis manifest in the relationships between neurophysiological measures, providing further evidence that asynchronous development along the S-A axis depends on maturation of brain function. New & NoteworthyWe report a novel developmental relationship between the human resting-state alpha rhythm frequency and the duration of intrinsic neural timescales. Using resting-state electrocorticography, we found that alpha frequency increased with age at either end of the sensorimotor-to-association cortical hierarchy, while intrinsic neural timescales only decreased with age in association regions. This negative correlation between alpha frequency and intrinsic timescale was only evident in association regions, further linking functional maturation and cortical hierarchy. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=154 SRC="FIGDIR/small/671637v1_ufig1.gif" ALT="Figure 1"> View larger version (54K): org.highwire.dtl.DTLVardef@151bd4dorg.highwire.dtl.DTLVardef@163403forg.highwire.dtl.DTLVardef@10f244eorg.highwire.dtl.DTLVardef@118a154_HPS_FORMAT_FIGEXP M_FIG C_FIG

neuroscience↗

Regulation of mannitol metabolism in Enterococcus faecalis and association with parEF0409 toxin-antitoxin locus function.

The parEF0409 type I toxin-antitoxin locus is situated between genes for two paralogous mannitol-family phosphoenolpyruvate phosphotransferase systems (PTS). In order to address the possibility that parEF0409 function was associated with sugar metabolism, genetic and phenotypic analyses were performed on the flanking genes. It was found that the genes were transcribed as two operons; the downstream operon essential for mannitol transport and metabolism and the upstream operon performing a regulatory function. In addition to genes for the PTS components, the upstream operon encodes a gene similar to mtlR, the key regulator of mannitol metabolism in other Gram-positive bacteria. We confirmed that this gene is essential for regulation of the downstream operon and identified putative phosphorylation sites required for carbon catabolite repression and mannitol-specific regulation. Genomic comparisons revealed that this dual operon organization of mannitol utilization genes is uncommon in enterococci and that association with a toxin-antitoxin system is unique to E. faecalis. Finally, we consider possible links between parEF0409 function and mannitol utilization. ImportanceEnterococcus faecalis is both a common member of the human gut microbiota and an opportunistic pathogen. Its evolutionary success is partially due to its metabolic flexibility: in particular, its ability to import and metabolize a wide variety of sugars. While a large number of phosphoenolpyruvate phosphotransferase sugar transport systems have been identified in the E. faecalis genome bioinformatically, the specificity and regulation of most of these systems remains undetermined. Here we characterize a complex system of two operons flanking a type I toxin-antitoxin system required for the transport and metabolism of the common dietary sugar mannitol. We also determine the phylogenetic distribution of mannitol utilization genes in the enterococcal genus and discuss the significance of association with toxin-antitoxin systems.

microbiology↗