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Fechner, J.

Publications and source records attributed to Fechner, J..

2 recordsLinked to original sources

Juvenile rat's sleep enables schema memory across episodes before expression of memory for individual episodes

Schema memory refers to generalized knowledge extracted from multiple related episodes. According to systems consolidation theory, such representations emerge during sleep through the transformation of hippocampus-dependent episodic memories into neocortical schema representations. Whether this process requires mature episodic memory expression during early development remains unclear. Here, we examined schema formation in infant rats with an immature hippocampus. At postnatal day (PD) 25, pups (n=24) were tested in an adapted object-place paradigm enabling abstraction of a spatial regularity across eight consecutive episodes. Following encoding, pups either slept or remained awake for two hours, and schema memory was tested 22 hours later. Control groups were exposed to pseudorandomized object configurations. Schema memory was expressed only after exposure to spatial regularities and only when sleep followed encoding. To directly assess episodic memory under comparable conditions, an additional group of pups (n=12) was tested in a standard single-episode object-place recognition (OPR) task with post-encoding sleep. At a 4-hours test, these pups did not show episodic object-place memory. These findings indicate that sleep supports schema memory formation during early life under conditions in which the expression of robust single-episode memory is not yet evident, suggesting that schema abstraction in infancy does not depend on fully developed hippocampal episodic representations.

neuroscience↗

Inhibition of Notch activity by phosphorylation of CSL in response to parasitization in Drosophila

Notch signalling activity regulates hematopoiesis in Drosophila and vertebrates alike. Parasitoid wasp infestation of Drosophila larvae, however, requires a timely downregulation of Notch activity to allow the formation of encapsulation-active blood cells. Here we show that the Drosophila CSL transcription factor Suppressor of Hairless [Su(H)] is phosphorylated at Serine 269 in response to parasitoid wasp infestation. As this phosphorylation interferes with the DNA-binding of Su(H), it reversibly precludes its activity. Accordingly, phospho-deficient Su(H)S269A mutants are immune compromised. A screen for kinases involved in Su(H) phosphorylation identified Pkc53E, required for normal hematopoiesis as well as for parasitoid immune response. Genetic and molecular interactions support the specificity of the Su(H)-Pkc53E relationship. Moreover, phorbol ester treatment inhibits Su(H) activity in vivo and in human cell culture. We conclude that Pkc53E targets Su(H) during parasitic wasp infestation, thereby remodeling the blood cell population required for wasp egg encapsulation.

developmental biology↗