Complementary DNA cloning, protein expression, and characterization of alpha-class GSTs from Macaca fascicularis

Charles Wang1, Theo K Bammler, David L Eaton

  • 1Cedars Sinai Medical Center, Davis Building G150, 8700 Beverly Blvd, Los Angeles, California 90048, USA.

Insights

Nonhuman primate alpha-class GSTs (mfaGSTA1-3) lack aflatoxin B(1)-8,9-epoxide detoxifying activity, similar to humans. This explains their resistance to aflatoxin B(1)-induced liver cancer, unlike rodents.

Area of Science:

  • Biochemistry
  • Toxicology
  • Genetics

Background:

  • Species-specific sensitivity to aflatoxin B(1) (AFB(1))-induced liver cancer is linked to glutathione S-transferase (GST) activity.
  • Mice are resistant due to high activity of alpha-class mGSTA3-3 towards AFB(1)-8,9-epoxide (AFBO), while rats are sensitive due to low levels of rGSTA5-5.

Purpose of the Study:

  • To investigate the AFBO-detoxifying activity of alpha-class GSTs in the nonhuman primate Macaca fascicularis (Mf).
  • To determine if Mf alpha-class GSTs possess the critical residues for high AFBO activity found in mouse GSTs.

Main Methods:

  • Constructed a cDNA library from Mf liver and screened it using human alpha-class GstA1 cDNA.
  • Identified and sequenced three full-length alpha-class GST clones (mfaGSTA1, mfaGSTA2, mfaGSTA3).
  • Expressed and characterized recombinant mfaGSTA1-1 protein for activity against GST substrates and AFBO.

Main Results:

  • Mf alpha-class GSTs (mfaGSTA1-3) showed high homology to each other and moderate identity to human GSTA1.
  • Recombinant mfaGSTA1-1 exhibited GST activity but lacked AFBO conjugating activity, similar to human GSTA1-1.
  • Mf alpha-class GSTs lacked the six critical residues associated with high AFBO activity in mouse GSTA3-3.

Conclusions:

  • Alpha-class GSTs from Macaca fascicularis have minimal AFBO conjugating activity, mirroring human GSTs.
  • This lack of activity contributes to the resistance of Mf to AFB(1)-induced hepatocarcinogenesis.
  • Findings highlight significant differences in AFB(1) metabolism and carcinogenicity between primates and rodents.

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