Literature DB >> 32181667

Quantitative Proteomics Reveals Distinct Molecular Signatures of Different Cerebellum-Dependent Learning Paradigms.

Yong Gyu Kim1,2, Jongmin Woo1,3, Joonho Park4, Sooyong Kim1,2, Yong-Seok Lee1,2,5, Youngsoo Kim1,4, Sang Jeong Kim1,2,5.   

Abstract

The cerebellum improves motor performance by adjusting motor gain appropriately. As de novo protein synthesis is essential for the formation and retention of memories, we hypothesized that motor learning in the opposite direction would induce a distinct pattern of protein expression in the cerebellum. We conducted quantitative proteomic profiling to compare the level of protein expression in the cerebellum at 1 and 24 h after training from mice that underwent different paradigms of cerebellum-dependent oculomotor learning from specific directional changes in motor gain. We quantified a total of 43 proteins that were significantly regulated in each of the three learning paradigms in the cerebellum at 1 and 24 h after learning. In addition, functional enrichment analysis identified protein groups that were differentially enriched or depleted in the cerebellum at 24 h after the three oculomotor learnings, suggesting that distinct biological pathways may be engaged in the formation of three oculomotor memories. Weighted correlation network analysis discovered groups of proteins significantly correlated with oculomotor memory. Finally, four proteins (Snca, Sncb, Cttn, and Stmn1) from the protein group correlated with the learning amount after oculomotor training were validated by Western blot. This study provides a comprehensive and unbiased list of proteins related to three cerebellum-dependent motor learning paradigms, suggesting the distinct nature of protein expression in the cerebellum for each learning paradigm. The proteomics data have been deposited to the ProteomeXchange Consortium with identifiers <PXD008433>.

Entities:  

Keywords:  Cerebellum; Motor memory; Optokinetic response (OKR); Proteome; TMT-labeled mass spectrometry; Vestibulo-ocular reflex (VOR)

Mesh:

Year:  2020        PMID: 32181667     DOI: 10.1021/acs.jproteome.9b00826

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  2 in total

1.  Decreased intrinsic excitability of cerebellar Purkinje cells following optokinetic learning in mice.

Authors:  Yong Gyu Kim; Sang Jeong Kim
Journal:  Mol Brain       Date:  2020-10-07       Impact factor: 4.041

2.  Kdm3b haploinsufficiency impairs the consolidation of cerebellum-dependent motor memory in mice.

Authors:  Yong Gyu Kim; Myeong Seong Bak; Ahbin Kim; Yujin Kim; Yun-Cheol Chae; Ye Lee Kim; Yang-Sook Chun; Joon-Yong An; Sang-Beom Seo; Sang Jeong Kim; Yong-Seok Lee
Journal:  Mol Brain       Date:  2021-07-03       Impact factor: 4.041

  2 in total

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