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Embryonic Expression and Function of the Xenopus Ink4d Cyclin D-Dependent Kinase Inhibitor.
Doherty, Joanne R; Nilsson, Lisa M; Kuliyev, Emin; Zhu, Haiqing; Matthew, Rose; Cleveland, John L; Mead, Paul E; Roussel, Martine F.
Afiliação
  • Doherty JR; Department of Pathology, St. Jude Children's Research Hospital, TN, USA.
  • Nilsson LM; Department of Biochemistry St. Jude Children's Research Hospital, TN, USA.
  • Kuliyev E; Department of Tumor Cell Biology, St. Jude Children's Research Hospital, TN, USA.
  • Zhu H; Department of Cancer Biology, The Scripps Research Institute, Scripps Florida, FL, USA.
  • Matthew R; Sahlgrenska Cancer Center, University of Gothenburg, Gothenburg, Sweden.
Cell Dev Biol ; 3(1)2014 Feb 15.
Article em En | MEDLINE | ID: mdl-25309971
ABSTRACT
Here we report the cloning and functional characterization of the cyclin D-dependent kinase 4 and 6 (Cdk4/6) inhibitory protein Cdkn2d/p19Ink4d of Xenopuslaevis (Xl-Ink4d). Xl-Ink4d is the only Ink4 family gene highly expressed during Xenopus development and its transcripts were detected maternally and during neurulation. The Xl-Ink4d protein has 63% identity to mouse and human Cdkn2d/p19Ink4d and its function as a negative regulator of cell cycle traverse is evolutionary conserved. Indeed, Xl-lnk4d can functionally substitute for mouse Cdkn2d in binding to mouse Cdk4 and inhibiting cyclin-D1-dependent CDK4 kinase activity. Further, enforced expression of Xl-lnk4d arrests mouse fibroblasts in the G1 phase of the cell cycle. These findings indicate that CDKN2d/p19Ink4d is conserved through vertebrate evolution and suggest Xl-lnk4d may contribute to the development of Xenopuslaevis.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cell Dev Biol Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Cell Dev Biol Ano de publicação: 2014 Tipo de documento: Article