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Cano, D. A.

Publications and source records attributed to Cano, D. A..

2 recordsLinked to original sources

PKMζ-KIBRA interactions, molecular turnover, and memory

How can the molecules that strengthen synaptic connections maintain memory in the face of molecular turnover? Our previous work showed that persistent interaction between the postsynaptic scaffolding protein, KIBRA, and the autonomously active PKC isoform, PKM{zeta}, is crucial for maintaining synaptic long-term potentiation (LTP) and memory for at least a month. This duration is longer than the lifespans of individual KIBRA and PKM{zeta} molecules. Biophysical modeling of the interaction suggests oligomers of KIBRA-PKM{zeta} dimers, but not individual dimers or monomers, can overcome molecular turnover by continually incorporating newly synthesized KIBRA and PKM{zeta}, replacing those that have degraded. Here we used AlphaFold 3 to predict the structures of KIBRA-PKM{zeta} heterodimers and heterohexamers and to examine the sites of action of two structurally distinct inhibitors of KIBRA-PKM{zeta} interaction that disrupt established late-LTP and long-term memory. The structures predict that the peptide K-ZAP blocks formation of heterodimers, whereas the small molecule {zeta}-stat prevents PKM{zeta} of one heterodimer from binding a second KIBRA and PKM{zeta}, essential for forming larger oligomeric structures. We show that {zeta}-stat, like K-ZAP, disrupts 1-month-old spatial memory. Thus, continual formation of KIBRA-PKM{zeta} oligomers can be a core molecular mechanism driving the persistence of long-term memory in the face of molecular turnover.

neuroscience↗

PKMζ-PKC{iota}/{lambda} double-knockout reveals the atypical PKCs are crucial for hippocampal late-LTP and spatial long-term memory

PKM{zeta}, a persistently active atypical PKC (aPKC) isoform, is thought to maintain late-phase long-term potentiation (late-LTP) and long-term memory. However, PKM{zeta}-knockout mice still exhibit hippocampal LTP and spatial memory while lacking neocortical LTP, questioning whether this kinase is fundamental to enduring synaptic potentiation and memory. Tsokas et al. (2016) showed the other aPKC, PKC{iota}/{lambda}, likely compensates for PKM{zeta} during maintenance in the hippocampus of PKM{zeta}-null mice. In wild-type mice, PKC{iota}/{lambda} drives early-LTP and short-term memory, while PKM{zeta} compensates for PKC{iota}/{lambda} knockout by supporting both early- and late-phase processes. Here we show PKC{iota}/{lambda} persistently increases during maintenance in two mouse models: PKM{zeta}-conditional knockout (cKO) mice, and double-knockout mice carrying both conditional deletion of PKC{iota}/{lambda} and constitutive loss of PKM{zeta}. In the double-knockout mice, PKC{iota}/{lambda} was measured while the kinase was still present, prior to its inducible ablation, to characterize its compensatory upregulation in late-LTP before removal. To test whether this compensation was functional, we ablated PKC{iota}/{lambda} in the hippocampus of the double-knockout mice. The double-knockout eliminated late-LTP, whereas individual knockout of either aPKC alone showed normal-appearing LTP. Double-knockout also abolished spatial long-term memory without affecting short-term memory. Thus, when PKM{zeta} is absent, PKC{iota}/{lambda} persists to maintain hippocampal late-LTP and long-term memory.

neuroscience↗