期刊论文详细信息
FEBS Letters
DNA binding protein dbpA binds Cdk5 and inhibits its activity
Zumstein-Mecker, Sabine1  Chaudhuri, Bhabatosh1  Moorthamer, Mark1 
[1] Oncology Research, Novartis Pharma AG, K-125.13.17, Basel, Switzerland
关键词: Cyclin dependant kinase 5;    DNA binding protein A;    Kinase inhibitor;    Yeast two-hybrid system;    β-gal;    β-galactosidase;    Cdk;    human cyclin dependent kinase;    CSD;    cold shock domain;    DBD;    DNA binding domain;    GSH-Sepharose;    glutathione Sepharose;    GST;    glutathione S-transferase;    p35;    35 kDa protein which activates Cdk5;    PCR;    polymerase chain reaction;    pRb;    human retinoblastoma protein;    RT;    room temperature;    SDS-PAGE;    sodium dodecyl sulfate-polyacrylamide gel electrophoresis;    TAD;    transcriptional activation domain;   
DOI  :  10.1016/S0014-5793(99)00248-3
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

Progress in the cell cycle is governed by the activity of cyclin dependent kinases (Cdks). Unlike other Cdks, the Cdk5 catalytic subunit is found mostly in differentiated neurons. Interestingly, the only known protein that activates Cdk5 (i.e. p35) is expressed solely in the brain. It has been suggested that, besides its requirement in neuronal differentiation, Cdk5 activity is induced during myogenesis. However, it is not clear how this activity is regulated in the pathway that leads proliferative cells to differentiation. In order to find if there exists any Cdk5-interacting protein, the yeast two-hybrid system was used to screen a HeLa cDNA library. We have determined that a C-terminal 172 amino acid domain of the DNA binding protein, dbpA, binds to Cdk5. Biochemical analyses reveal that this fragment (dbpA(CΔ)) strongly inhibits p35-activated Cdk5 kinase. The protein also interacts with Cdk4 and inhibits the Cdk4/cyclin D1 enzyme. Surprisingly, dbpA(CΔ) does not bind Cdk2 in the two-hybrid assay nor does it inhibit Cdk2 activated by cyclin A. It could be that dbpA's ability to inhibit Cdk5 and Cdk4 reflects an apparent cross-talk between distinct signal transduction pathways controlled by dbpA on the one hand and Cdk5 or Cdk4 on the other.

【 授权许可】

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