Editors' ChoiceNeuroscience

Papers of note in Nature 551 (7679)

See allHide authors and affiliations

Sci. Signal.  14 Nov 2017:
Vol. 10, Issue 505, eaar4560
DOI: 10.1126/scisignal.aar4560

This week’s articles highlight interactions between astrocytes and neurons that influence both cell types’ form and function; a genetic basis for individual variation in aging; and the mechanism by which an E3 ubiquitin ligase adaptor affects synaptic transmission.

NEUROSCIENCE

Astrocyte-neuron contacts

Stogsdill et al. show that the interaction between astrocyte neuroligins and neuronal neurexins controls both astrocyte morphology and synaptogenesis.

Natural variation and aging

Yin et al. report that polymorphisms in a neuropeptide-encoding gene underlie differences in aging between individual nematodes (see also McGrath).

Degrading RhoA for synaptic transmission

Escamilla et al. demonstrate that loss of the E3 ubiquitin ligase adaptor KCTD13 reduces synaptic transmission by increasing the accumulation of the small GTPase RhoA. Copy number variations in Kctd13 have been linked to neuropsychiatric and neurodevelopmental disorders, suggesting RhoA as a potential therapeutic target for treating disorders in which Kctd13 is deleted.

Highlighted Articles

View Abstract

Navigate This Article