Proteomics

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Identification of the methyl-CpG binding protein 2 (MeCP2) interacting proteins in the high molecular weight (HMW) extract prepared from the human HEK293T cells by immunoprecipitation coupled with mass spectrometry analysis


ABSTRACT: Identification of MeCP2 interacting proteins in HMW extract of HEK293T cells

ORGANISM(S): Homo Sapiens

SUBMITTER: Jingyi Hui  

PROVIDER: PXD021650 | iProX | Mon Aug 30 00:00:00 BST 2021

REPOSITORIES: iProX

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Publications

Rett syndrome linked to defects in forming the MeCP2/Rbfox/LASR complex in mouse models.

Jiang Yan Y   Fu Xing X   Zhang Yuhan Y   Wang Shen-Fei SF   Zhu Hong H   Wang Wei-Kang WK   Zhang Lin L   Wu Ping P   Wong Catherine C L CCL   Li Jinsong J   Ma Jinbiao J   Guan Ji-Song JS   Huang Ying Y   Hui Jingyi J  

Nature communications 20211001 1


Rett syndrome (RTT) is a severe neurological disorder and a leading cause of intellectual disability in young females. RTT is mainly caused by mutations found in the X-linked gene encoding methyl-CpG binding protein 2 (MeCP2). Despite extensive studies, the molecular mechanism underlying RTT pathogenesis is still poorly understood. Here, we report MeCP2 as a key subunit of a higher-order multiunit protein complex Rbfox/LASR. Defective MeCP2 in RTT mouse models disrupts the assembly of the MeCP2/  ...[more]

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