Zebrafish Thymidylate Synthase Binds to Its Own mRNA in vitro and in vivo
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This work was supported by grant from The National Natural Science Foundation of China (40506031, 30472043) and Natural Science Foundation of Shandong Province (Q2005C06).

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    Abstract:

    Thymidylate synthase (TS), an essential enzyme for DNA de novo synthesis, is a critical therapeutic target in cancer therapy. Previous study has shown that TS was able to bind to its own mRNA in human and E.coli, resulting in translational repression. Zebrafish is the best animal model for vertebrate study. In order to study the regulatory mechanism of zebrafish TS, the enzyme were expressed in E. coli BL21 (DE3) and it was purified to homogeneity. Electrophoretic mobility shift assay (EMSA) was used to detect the interaction of zebrafish TS protein and its own TS transcript in vitro and the results showed that zebrafish TS could bound with its own mRNA specifically. Further study revealed that zebrafish TS was able to interact with its own mRNA in vivo using immunoprecipitation : RT-PCR technique. The results provide evidence that zebrafish may be developed as an useful model for studying the anti-metabolism agents.

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SONG Chun-Xia, NIU Rong-Li, DU Chang-Qing, YANG Shao-Li, LIN Xiu-Kun. Zebrafish Thymidylate Synthase Binds to Its Own mRNA in vitro and in vivo[J]. Progress in Biochemistry and Biophysics,2007,34(12):1321-1326

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History
  • Received:May 22,2007
  • Revised:August 30,2007
  • Accepted:
  • Online: September 04,2007
  • Published: