Transcriptional Regulation of the Schizosaccharomyces pombe Gene Encoding Glutathione S-Transferase I by a Transcription Factor Pap1

  • Kim Hong-Gyum (Division of Life Sciences. College of Natural Sciences. Kangwon National University) ;
  • Kim Byung-Chul (Division of Life Sciences. College of Natural Sciences. Kangwon National University) ;
  • Kim Kyunghoon (Division of Life Sciences. College of Natural Sciences. Kangwon National University) ;
  • Park Eun-Hee (College of Pharmacy, Sookmyung Women`s University) ;
  • Lim Chang-Jin (Division of Life Sciences. College of Natural Sciences. Kangwon National University)
  • Published : 2004.12.01

Abstract

In a previous study, a gst gene was isolated from the fission yeast Schizosaccharomyces pombe. This gene was dubbed gstI, and was characterized using the gstI -lacZ fusion plasmid pYSH2000. In this work, four additional fusion plasmids, pYSHSDl, pYSHSD2, pYSHSD3 and pYSHSD4, were constructed, in order to carry (respectively) 770, 551, 358 and 151 bp upstream regions from the translational initiation point. The sequence responsible for induction by aluminum, mercury and hydrogen peroxide was located in the range between -1,088 and -770 bp upstream of the S. pombe gstI gene. The same region was identified to contain the nucleotide sequence responsible for regulation by Papl, and has one puta­tive Papl binding site, TTACGTAT, located in the range between $-954\~-947$ bp upstream of the gstI gene. Negatively acting sequences are located between -1,088 and -151 bp. These findings imply that the Papl protein is involved in basal and inducible transcription of the gstI gene in the fission yeast S. pombe.

Keywords

References

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