Identification of murine cdk10: Association with Ets2 transcription factor and effects on the cell cycle

被引:15
作者
Bagella, Luigi
Giacinti, Cristina
Simone, Cristiano
Giordano, Antonio
机构
[1] Temple Univ, Sbarro Inst Canc Res & Mol Med, Coll Sci & Technol, Philadelphia, PA 19122 USA
[2] Univ Siena, Nuovo Policlin Le Scotte, Dept Human Pathol & Oncol, I-53100 Siena, Italy
[3] Univ Bari, Div Med Genet, Dept Biomed Childhood, I-70121 Bari, Italy
[4] Univ Sassari, Div Biochem, Dept Biomed Sci, I-07100 Sassari, Italy
关键词
cdk10; splice variant; cell cycle; cdks;
D O I
10.1002/jcb.20981
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cyclin-dependent kinases (cdks) are the catalytic subunits of a large family of serine/threonine protein kinases whose best-characterized members are key regulators of eukaryotic cell cycle progression. They are activated by binding to regulatory subunits generally termed as cyclins. Cdk10 is a cdc2-related kinase that contains the canonical regulatory Tyr and Thr residues present in all protein kinases and a PSTAIRE-like motif named PISSLRE. Although little is known about this protein, human cdk10 has been shown to encode two different isoforms, each having a distinct function. They differ at both the carboxy- and amino-terminals, although most of the amino acid sequence is predicted to be identical for the two isoforms. A role at the G2/M transition has been suggested for an isoform of cdk10, while the alternative splicing form interacts with the N-terminus of the Ets2 transcription factor. Here we report the cloning and the functional characterization of a cDNA encoding the murine homologue of cdk10. Unlike its human counterpart, only one murine cdk10 protein has been identified, and this unique murine cdk10 cDNA encodes a putative protein of 360 amino acids. Comparison of the amino acid sequences of murine and human cdk10 shows high homology. Murine cdk10 binds Ets2 transcription factors in vitro, does not show a direct involvement in the G2/M transition and, therefore, does not affect the proliferation rate of the cell lines analyzed.
引用
收藏
页码:978 / 985
页数:8
相关论文
共 36 条
[1]  
Bagella L, 1998, J CELL PHYSIOL, V177, P206, DOI 10.1002/(SICI)1097-4652(199811)177:2<206::AID-JCP2>3.0.CO
[2]  
2-R
[3]   Mechanisms of alternative pre-messenger RNA splicing [J].
Black, DL .
ANNUAL REVIEW OF BIOCHEMISTRY, 2003, 72 :291-336
[4]  
BRAMBILLA R, 1994, ONCOGENE, V9, P3037
[5]   Exon scrambling of MLL transcripts occur commonly and mimic partial genomic duplication of the gene [J].
Caldas, C ;
So, CW ;
MacGregor, A ;
Ford, AM ;
McDonald, B ;
Chan, LC ;
Wiedemann, LM .
GENE, 1998, 208 (02) :167-176
[6]   Identification and characterization of the CDK12/cyclin L1 complex involved in alternative splicing regulation [J].
Chen, HH ;
Wang, YC ;
Fann, MJ .
MOLECULAR AND CELLULAR BIOLOGY, 2006, 26 (07) :2736-2745
[7]   SPLICING WITH INVERTED ORDER OF EXONS OCCURS PROXIMAL TO LARGE INTRONS [J].
COCQUERELLE, C ;
DAUBERSIES, P ;
MAJERUS, MA ;
KERCKAERT, JP ;
BAILLEUL, B .
EMBO JOURNAL, 1992, 11 (03) :1095-1098
[8]   The PISSLRE gene:: Structure, exon skipping, and exclusion as tumor suppressor in breast cancer [J].
Crawford, J ;
Ianzano, L ;
Savino, M ;
Whitmore, S ;
Cleton-Jansen, AM ;
Settasatian, C ;
d'Apolito, M ;
Seshadri, R ;
Pronk, JC ;
Auerbach, AD ;
Verlander, PC ;
Mathew, CG ;
Tipping, AJ ;
Doggett, NA ;
Zelante, L ;
Callen, DF ;
Savoia, A .
GENOMICS, 1999, 56 (01) :90-97
[9]   A unique domain of pRb2/p130 acts as an inhibitor of Cdk2 kinase activity [J].
DeLuca, A ;
MacLachlan, TK ;
Bagella, L ;
Dean, C ;
Howard, CM ;
Claudio, PP ;
Baldi, A ;
Khalili, K ;
Giordano, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (34) :20971-20974
[10]   IDENTIFICATION OF P34 AND P13, HUMAN HOMOLOGS OF THE CELL-CYCLE REGULATORS OF FISSION YEAST ENCODED BY CDC2+ AND SUC1+ [J].
DRAETTA, G ;
BRIZUELA, L ;
POTASHKIN, J ;
BEACH, D .
CELL, 1987, 50 (02) :319-325