首页> 外文OA文献 >Preferential over-expression of the class alpha rat Ya2 glutathione S-transferase subunit in livers bearing aflatoxin-induced pre-neoplastic nodules. Comparison of the primary structures of Ya1 and Ya2 with cloned class alpha glutathione S-transferase cDNA sequences.
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Preferential over-expression of the class alpha rat Ya2 glutathione S-transferase subunit in livers bearing aflatoxin-induced pre-neoplastic nodules. Comparison of the primary structures of Ya1 and Ya2 with cloned class alpha glutathione S-transferase cDNA sequences.

机译:在患有黄曲霉毒素诱导的肿瘤前结节的肝脏中,α类大鼠Ya2谷胱甘肽S-转移酶亚基的优先过表达。 Ya1和Ya2的一级结构与克隆的α型谷胱甘肽S-转移酶cDNA序列的比较。

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摘要

Normal rat liver expresses Ya (Mr 25,500), Yc (Mr 27,500) and Yk (Mr 25,000) Class Alpha glutathione S-transferase (GST) subunits. The Ya-type subunit can be resolved into two separate polypeptides, designated Ya1 and Ya2, by reverse-phase h.p.l.c. In rat livers that possess aflatoxin B1-induced pre-neoplastic nodules, a marked increase is observed in the expression of Ya1, Ya2, Yc and Yk; of these subunits, Ya2 exhibited the greatest increase in concentration. The Ya1 and Ya2 subunits isolated from nodule-bearing livers were cleaved with CNBr, and the purified peptides were subjected to automated amino-acid-sequence analysis. Differences in the primary structures of the two Ya GST subunits were found at positions 31, 34, 107 and 117. These data demonstrate that Ya1 and Ya2 are distinct polypeptides and are the products of separate genes. The amino acid sequences obtained from Ya1 and Ya2 were compared with the cloned cDNAs pGTB 38 [Pickett, Telakowski-Hopkins, Ding, Argenbright & Lu (1984) J. Biol. Chem. 259, 4112-4115] and pGTR 261 [Lai, Li, Weiss, Reddy & Tu (1984) J. Biol. Chem. 259, 5182-5188], which encode rat Ya-type subunits. From these comparisons it appears probable that Ya1 represents the GST subunit encoded by pGTR 261, whereas Ya2 represents the subunit encoded by pGTB 38. It is likely that the over-expression of Ya1 and Ya2 in nodule-bearing livers is of major significance in the acquired resistance of nodules to aflatoxin B1, since previous work [Coles, Meyer, Ketterer, Stanton & Garner (1985) Carcinogenesis 6, 693-697] has shown that the Ya-type GST subunit has high activity towards aflatoxin B1 8,9-epoxide.
机译:正常大鼠肝脏表达Ya(Mr 25,500),Yc(Mr 27,500)和Yk(Mr 25,000)类Alpha谷胱甘肽S-转移酶(GST)亚基。通过反相h.p.l.c,可以将Ya型亚基分解为两个分开的多肽,命名为Ya1和Ya2。在具有黄曲霉毒素B1诱导的肿瘤前结节的大鼠肝脏中,观察到Ya1,Ya2,Yc和Yk的表达明显增加;在这些亚基中,Ya2的浓度增加最大。从结节性肝中分离的Ya1和Ya2亚基用CNBr裂解,并对纯化的肽进行自动氨基酸序列分析。在位置31、34、107和117处发现了两个Ya GST亚基的一级结构的差异。这些数据表明Ya1和Ya2是不同的多肽,并且是不同基因的产物。将从Ya1和Ya2获得的氨基酸序列与克隆的cDNA pGTB 38进行比较[Pickett,Telakowski-Hopkins,Ding,Argenbright&Lu(1984)J.Biol.Chem。化学259,4112-4115]和pGTR 261 [Lai,Li,Weiss,Reddy&Tu(1984)J.化学259,5182-5188],其编码大鼠Ya型亚基。从这些比较看来,Ya1可能代表由pGTR 261编码的GST亚基,而Ya2代表由pGTB 38编码的亚基。自从以前的工作[Coles,Meyer,Ketterer,Stanton&Garner(1985)Carcinogenesis 6,693-697]以来,Ya型结节对黄曲霉毒素B1产生了抗药性,显示Ya型GST亚基对黄曲霉毒素B1 8,9-具有很高的活性。环氧。

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