TY - JOUR
T1 - Significant induction of a 54-kDa protein in rat liver with homologous alignment to mouse selenium binding protein by a coplanar polychlorinated biphenyl, 3,4,5,3',4'pentachlorobiphenyl and 3-methylcholanthrene
AU - Ishii, Yuji
AU - Hatsumura, Megumu
AU - Ishida, Takumi
AU - Ariyoshi, Noritaka
AU - Oguri, Kazuta
PY - 1996/9
Y1 - 1996/9
N2 - A 54-kDa protein in rat liver cytosol was significantly induced by treatment with 3,4,5,3',4' -pentachlorobiphenyl (25 mg/kg, single i.p.) and 3-methylcholanthrene (20 mg/kg, once a day for 3 days, i.p.). The protein exhibited pI of 6.8 on two-dimensional gel electrophoresis. The amino acid sequences of peptide fragments from the protein digested in situ were highly similar to a selenium binding protein in mice and to the isoform acetaminophen binding protein in mice. The present result clearly demonstrates that a coplanar polychlorinated biphenyl and 3-methylcholanthrene are responsible for induction of selenium binding protein homologues. The physiological role of the mouse proteins, however, is not yet elucidated.
AB - A 54-kDa protein in rat liver cytosol was significantly induced by treatment with 3,4,5,3',4' -pentachlorobiphenyl (25 mg/kg, single i.p.) and 3-methylcholanthrene (20 mg/kg, once a day for 3 days, i.p.). The protein exhibited pI of 6.8 on two-dimensional gel electrophoresis. The amino acid sequences of peptide fragments from the protein digested in situ were highly similar to a selenium binding protein in mice and to the isoform acetaminophen binding protein in mice. The present result clearly demonstrates that a coplanar polychlorinated biphenyl and 3-methylcholanthrene are responsible for induction of selenium binding protein homologues. The physiological role of the mouse proteins, however, is not yet elucidated.
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U2 - 10.1016/0378-4274(96)03668-5
DO - 10.1016/0378-4274(96)03668-5
M3 - Article
C2 - 8701438
AN - SCOPUS:0030246985
SN - 0378-4274
VL - 87
SP - 1
EP - 9
JO - Toxicology Letters
JF - Toxicology Letters
IS - 1
ER -