SMRT as a T3SF-binding protein

  • Authors:
    • Kotaro Onishi
    • Mitsuo V. Kato
    • Fulu Bai
    • Toshiyuki Sakai
  • View Affiliations

  • Published online on: May 1, 2001     https://doi.org/10.3892/ijo.18.5.985
  • Pages: 985-989
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Abstract

p53-binding consensus-like sequence (T3SF) is located in the murine promoter region of tissue inhibitor of metalloproteinase 3 gene. To identify the genes that encode proteins that bind to T3SF DNA sequence, we screened a cDNA library using the Southwestern technique. The SMRT gene was cloned as one of the candidates. Addition of antibody against SMRT reduced the intensity of a band that is supposed to contain SMRT in electrophoresis mobility shift assay, although antibody against p53 had no effect. Ultraviolet (UV)-irradiation reduced the intensity of the SMRT complex whereas p53 complex was stabilized by UV-irradiation. These results suggest that SMRT may bind to T3SF sequence in p53-independent manner and dissociate from the sequence by UV irradiation.

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May 2001
Volume 18 Issue 5

Print ISSN: 1019-6439
Online ISSN:1791-2423

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Spandidos Publications style
Onishi K, Kato MV, Bai F and Sakai T: SMRT as a T3SF-binding protein. Int J Oncol 18: 985-989, 2001
APA
Onishi, K., Kato, M.V., Bai, F., & Sakai, T. (2001). SMRT as a T3SF-binding protein. International Journal of Oncology, 18, 985-989. https://doi.org/10.3892/ijo.18.5.985
MLA
Onishi, K., Kato, M. V., Bai, F., Sakai, T."SMRT as a T3SF-binding protein". International Journal of Oncology 18.5 (2001): 985-989.
Chicago
Onishi, K., Kato, M. V., Bai, F., Sakai, T."SMRT as a T3SF-binding protein". International Journal of Oncology 18, no. 5 (2001): 985-989. https://doi.org/10.3892/ijo.18.5.985