Literature DB >> 10607900

Sak kinase gene structure and transcriptional regulation.

J W Hudson1, L Chen, C Fode, C Binkert, J W Dennis.   

Abstract

The Sak gene encodes a serine/threonine kinase, which is a member of the Polo family of mitotic regulators. Sak transcripts are present in S/G2/M phase cells, and in proliferating cell layers of the mouse embryo and adult tissues. In this report, we have characterized the murine Sak gene structure, the Sak chromosomal location, and identified the promoter. The murine Sak gene is located on the proximal arm of mouse chromosome 13, as determined by RFLP analysis. The murine gene comprises 15 coding exons spanning 16kb of genomic sequence, and encodes two alternately spliced transcripts. Sak-a, the predominant transcript, is encoded by 15 exons, while early termination of transcription and alternative splicing at exons 5 and 6 results in Sak-b. This truncated transcript encodes the complete kinase domain and a carboxyl end translated from 147bp of sequence contiguous with exon 5. Human Sak-a (Stk18) cDNA is reported to contain an insertion of sequence corresponding to the mouse Sak-b tail. Primer extension analysis of murine Sak revealed one major transcription start site at position -303bp relative to the start of translation. A genomic fragment of 3.5kb located 5' of the Sak transcriptional start drives expression of a luciferase-reporter gene in CHO and GC1-SPG cells in an orientation-dependent fashion. Using various Sak promoter/luciferase constructs, the core promoter region required for expression was located within 400bp of the message Cap site, and sequence further 5' strongly suppressed transcription.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10607900     DOI: 10.1016/s0378-1119(99)00467-9

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  6 in total

1.  SAK, a new polo-like kinase, is transcriptionally repressed by p53 and induces apoptosis upon RNAi silencing.

Authors:  Jun Li; Mingjia Tan; Ling Li; Deepika Pamarthy; Theodore S Lawrence; Yi Sun
Journal:  Neoplasia       Date:  2005-04       Impact factor: 5.715

Review 2.  Multifaceted polo-like kinases: drug targets and antitargets for cancer therapy.

Authors:  Klaus Strebhardt
Journal:  Nat Rev Drug Discov       Date:  2010-08       Impact factor: 84.694

3.  Reovirus-induced alterations in gene expression related to cell cycle regulation.

Authors:  George J Poggioli; Roberta L DeBiasi; Ryan Bickel; Robert Jotte; Aaron Spalding; Gary L Johnson; Kenneth L Tyler
Journal:  J Virol       Date:  2002-03       Impact factor: 5.103

4.  BCL2 translocation defines a unique tumor subset within the germinal center B-cell-like diffuse large B-cell lymphoma.

Authors:  Javeed Iqbal; Warren G Sanger; Douglas E Horsman; Andreas Rosenwald; Diane L Pickering; Bhavana Dave; Sandeep Dave; Li Xiao; Kajia Cao; Quiming Zhu; Simon Sherman; Christine P Hans; Dennis D Weisenburger; Timothy C Greiner; Randy D Gascoyne; German Ott; H Konrad Müller-Hermelink; Jan Delabie; Rita M Braziel; Elaine S Jaffe; Elias Campo; James C Lynch; Joseph M Connors; Julie M Vose; James O Armitage; Thomas M Grogan; Louis M Staudt; Wing C Chan
Journal:  Am J Pathol       Date:  2004-07       Impact factor: 4.307

5.  The novel mouse Polo-like kinase 5 responds to DNA damage and localizes in the nucleolus.

Authors:  Zdenek Andrysik; William Z Bernstein; Li Deng; David L Myer; Ya-Qin Li; Jay A Tischfield; Peter J Stambrook; El Mustapha Bahassi
Journal:  Nucleic Acids Res       Date:  2010-01-25       Impact factor: 16.971

6.  SmSak, the second Polo-like kinase of the helminth parasite Schistosoma mansoni: conserved and unexpected roles in meiosis.

Authors:  Thavy Long; Mathieu Vanderstraete; Katia Cailliau; Marion Morel; Arlette Lescuyer; Nadege Gouignard; Christoph G Grevelding; Edith Browaeys; Colette Dissous
Journal:  PLoS One       Date:  2012-06-29       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.