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首页> 外文期刊>Bulletin of experimental biology and medicine >Induction of Alternative Splicing and Inhibition of Activity of Telomerase Catalytic Subunit by Apoptotic Endonuclease EndoG in Human T, B, and NK Cells
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Induction of Alternative Splicing and Inhibition of Activity of Telomerase Catalytic Subunit by Apoptotic Endonuclease EndoG in Human T, B, and NK Cells

机译:通过凋亡内切核酸酶在人T,B和NK细胞中诱导替代剪接和抑制端粒酶催化亚基活性的抑制作用

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The effect of apoptotic endonuclease EndoG on alternative splicing of mRNA of human telomerase catalytic subunit hTERT (human telomerase reverse transcriptase) and telomerase activity in normal human lymphocytes were studied. Human CD4(+), CD8(+), B, and NK cells were transfected with a plasmid pEndoG-GFP containing EndoG gene or control plasmid pGFP. The levels of mRNA of EndoG or hTERT splicing variants were analyzed by real-time PCR. Protein content was assessed by Western blotting. Telomerase activity was measured by the telomere repeats amplification protocol. EndoG overexpression reduced the expression of active full-length hTERT and increased the expression of inactive splice variant. Shifted balance of hTERT splice variants in cells led to a significant decrease in telomerase activity within 72 h after transfection.
机译:研究了凋亡内切核酸酶的效果在正常人淋巴细胞中,研究了人端粒酶催化亚单元HTERT(人端粒酶逆转录酶)和端粒酶活性的MRNA替代剪接。 用含有engoG基因或对照质粒pGFP的质粒栓蛋白-GFP转染人CD4(+),CD8(+),B和NK细胞。 通过实时PCR分析了NupoG或HTERT剪接变体的mRNA水平。 通过蛋白质印迹评估蛋白质含量。 通过端粒重复扩增方案测量端粒酶活性。 Endog过度表达降低了活性全长HTETT的表达并增加了无活性剪接变体的表达。 HTERT接头变体的移动平衡在转染后72小时内的端粒酶活性显着降低。

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