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Transcription inhibition of the somatic-type phosphoglycerate kinase 1 gene in vitro by a testis-specific factor that recognizes a sequence similar to the binding site for Ets oncoproteins.

机译:睾丸特异性因子在体外抑制体细胞型磷酸甘油酸激酶1基因的转录,该因子识别与Ets癌蛋白结合位点相似的序列。

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摘要

To elucidate the mechanism by which transcription of the somatic-type phosphoglycerate kinase 1 gene is inactivated during mammalian spermatogenesis, we examined the presence of specific transcription inhibitor(s) in the testis by a cell-free transcription system. Transcription of the mouse phosphoglycerate kinase 1 gene using nuclear extracts of the rat liver was significantly inhibited by the addition of testis extracts, whereas brain extracts had little effect. Transcription inhibition required the binding of a testis-specific factor, designated TIN-1, to the region between positions -268 and -259 relative to transcription initiation site at +1. This region had the sequence 5'-AGGAAGTTCC-3' that includes an inverted repeat of the binding motif, 5'-GGAA-3', for the oncoprotein Ets. A UV-crosslinking experiment revealed that 43- and 45-kDa polypeptides present in testis extracts bind to that sequence. These results suggest that a testis-specific transcription inhibitor TIN-1 inactivates the phosphoglycerate kinase 1 gene in the mammalian spermatogenic pathway.
机译:为了阐明哺乳动物精子发生过程中体细胞型磷酸甘油酸激酶1基因转录失活的机制,我们通过无细胞转录系统检查了睾丸中特定转录抑制剂的存在。添加睾丸提取物显着抑制了使用大鼠肝核提取物对小鼠磷酸甘油酸激酶1基因的转录,而脑提取物的作用很小。转录抑制需要睾丸特异性因子TIN-1与相对于转录起始位点+1的-268和-259之间的区域结合。该区域具有序列5'-AGGAAGTTCC-3',该序列包括针对癌蛋白Ets的结合基序5'-GGAA-3'的反向重复。紫外线交联实验表明,睾丸提取物中存在的43 kDa和45 kDa多肽与该序列结合。这些结果表明,睾丸特异性转录抑制剂TIN-1使哺乳动物生精途径中的磷酸甘油酸激酶1基因失活。

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