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zhou, j.

Publications and source records attributed to zhou, j..

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Global and cross-omics feature aggregation improves single-cell multi-omics integration and clustering

Sequencing technology advancements enable the simultaneous measurement of multiple omics within single cells, thereby facilitating single-cell multi-omics analysis. Most existing deep multi-omics integration methods learn shared or omics-specific representations from multiple omics by omics-wise aggregation. However, these approaches often fail to account for the structural relationships among all cells. Here, we introduce scCODI, an innovative cross-omics deep learning model to integrate single-cell multi-omics data for cell clustering. This model processes paired omics datasets, combining single-cell transcriptomics with either epigenomics or proteomics data to facilitate a more comprehensive exploration of cellular heterogeneity. Specifically, the shared representation of two omics is derived through cross-omics feature aggregation, fully leveraging the complementarity of different omics within the same cell. Additionally, we align the omic-specific and shared representations of each cell using a global relationship-guided contrastive learning module, which enhances the similarity between the shared and omic-specific representations of the same cell. Extensive experiments demonstrate that scCODI outperforms previous methods in single-cell multi-omics data integration and cell clustering, as evidenced by its performance across nine paired multi-omics datasets. This makes it a promising tool for decoding complex biological mechanisms. The code is available at https://github.com/SXUI-BDSI/scCODI

bioinformatics↗

CaMKII autophosphorylation but not downstream kinase activity is required for synaptic memory

CaMKII plays a critical role in long-term potentiation (LTP), a well-established model for learning and memory through the enhancement of synaptic transmission. Biochemical studies indicate that CaMKII catalyzes a phosphotransferase (kinase) reaction of both itself (autophosphorylation) and of multiple downstream target proteins. However, whether either type of phosphorylation plays any role in the synaptic enhancing action of CaMKII remains hotly contested. We have designed a series of experiments to define the minimal requirements for the synaptic enhancement by CaMKII. We find that autophosphorylation of T286 and further binding of CaMKII to the GluN2B subunit are required both for initiating LTP and for its maintenance (synaptic memory). Once bound to the NMDA receptor, the synaptic action of CaMKII occurs in the absence of kinase activity. Thus, autophosphorylation, together with binding to the GluN2B subunit, are the only two requirements for CaMKII in synaptic memory.

neuroscience↗