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首页> 外文期刊>Molecular and Cellular Biology >Evidence for a stem cell-specific repressor of Moloney murine leukemia virus expression in embryonal carcinoma cells.
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Evidence for a stem cell-specific repressor of Moloney murine leukemia virus expression in embryonal carcinoma cells.

机译:莫洛尼鼠白血病病毒在胚胎癌细胞中表达的干细胞特异性阻遏物的证据。

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摘要

A negative regulatory element (NRE) spanning the tRNA primer-binding site (PBS) of Moloney murine leukemia virus (M-MuLV) mediates repression of M-MuLV expression specifically in embryonal carcinoma (EC) cells. We precisely defined the element by base-pair mutagenesis to an 18-base-pair segment of the tRNA PBS and showed that the element also restricted expression when moved upstream of the long terminal repeat. A DNA-binding activity specific for the M-MuLV NRE was detected in vitro by using crude EC nuclear extracts in exonuclease III protection assays. Binding was strongly correlated with repression in EC cells. Mutations within the NRE that relieved repression disrupted binding activity. Also, nuclear extracts prepared from permissive, differentiated EC cell cultures showed reduced binding activity for the NRE. These results indicate the presence of a stem cell-specific repressor that extinguishes M-MuLV expression via the NRE at the tRNA PBS.
机译:横跨莫洛尼氏鼠白血病病毒(M-MuLV)的tRNA引物结合位点(PBS)的负调控元件(NRE)介导了M-MuLV表达的抑制,特别是在胚胎癌细胞(EC)中。我们通过对tRNA PBS的18个碱基对区段的碱基对诱变精确地定义了该元件,并显示了该元件在移至长末端重复序列的上游时也限制了表达。通过在核酸外切酶III保护试验中使用粗制EC核提取物在体外检测到M-MuLV NRE特异的DNA结合活性。结合与EC细胞中的抑制作用密切相关。 NRE中减轻阻抑作用的突变破坏了结合活性。同样,从允许的,分化的EC细胞培养物中制备的核提取物显示出对NRE的结合活性降低。这些结果表明存在干细胞特异性阻遏物,该阻遏物通过tRNA PBS处的NRE消除M-MuLV表达。

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