AI Article Synopsis

  • - A probe based on rat glutathione S-transferase P (GST-P) cDNA was used to identify a human GST-pi clone in a complementary DNA library, revealing a complete coding sequence of 630 base pairs.
  • - The study determined the amino acid sequence of GST-pi, which is made up of 209 amino acids and has a molecular weight of about 23,224, showing significant similarity to the rat GST-P subunit.
  • - Differences in amino acids between GST-pi and GST-P contributed to variations in their isoelectric points and expression patterns in various human tissues compared to rats, particularly indicating distinct expression in cancerous tissues.

Article Abstract

We have used a rat glutathione S-transferase P (GST-P) complementary DNA as a probe to screen a human placenta complementary DNA library constructed in the lambda gt11 vector. One of the positive clones contained the complete coding region (630 base pair) and the entire 3'-noncoding region (78 base pair) of the putative human glutathione S-transferase pi (GST-pi) subunit mRNA. From the nucleotide sequence we deduced the complete amino acid sequence of the GST-pi subunit. It contained 209 amino acids with the relative molecular mass of Mr 23,224. Comparison of the amino acid sequences between GST-pi and GST-P subunits suggests that they are the corresponding enzymes in these species. GST-pi and GST-P both consist of 209 amino acids and differ in only 30 amino acids (85.6% homology). The difference in amino acid composition can explain the large difference in isoelectric point between GST-pi subunit (pI 5.5) and GST-P subunit (pI 6.9). The expression of GST-pi mRNA in some normal and cancerous tissues, including some hepatoma cell lines, hepatoma, and colon carcinoma specimens was determined using complementary DNA as a probe. The results indicate that the mode of the expression of GST-pi in humans is different from that of GST-P in rats.

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