首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >INHIBITION OF HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 TRANSCRIPTION AND REPLICATION BY DNA SEQUENCE-SELECTIVE PLANT LIGNANS
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INHIBITION OF HUMAN IMMUNODEFICIENCY VIRUS TYPE 1 TRANSCRIPTION AND REPLICATION BY DNA SEQUENCE-SELECTIVE PLANT LIGNANS

机译:DNA序列选择植物木质素的抑制1型人免疫缺陷病毒的转录和复制

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摘要

A plant lignan, 3'-O-methyl nordihydroguaiaretic acid (3'-O-methyl NDGA, denoted Malachi 4:5-6 or Mal.4; molecular weight 316), was isolated from Larrea tridentata and found to be able to inhibit human immunodeficiency virus (HIV) Tat-regulated transactivation in vivo, induce protection of lymphoblastoid CEM-SS cells from HIV (strain IIIB) killing, and suppress the replication of five HIV-1 strains (WM, MN, VS, JR-CSF, and IlI(B)) in mitogen-stimulated peripheral blood mononuclear cells, all in a dose-dependent manner. Mal.4 inhibits both basal transcription and Tat-regulated transactivation in vitro. The target of Mal.4 has been localized to nucleotides -87 to -40 of the HIV long terminal repeat, Mal.4 directly and specifically interferes with the binding of Spl to Spl sites in the HIV long terminal repeat, By inhibiting proviral expression, Mal.4 may be able to interrupt the life cycles of both wild-type and reverse transcriptase or protease mutant viruses in HIV-infected patients. [References: 29]
机译:从Larrea tridentata中分离出一种植物木脂体3'-O-甲基去氢二氢愈创木酸(3'-O-甲基NDGA,表示为Malachi 4:5-6或Mal.4;分子量为316),并且能够抑制人类免疫缺陷病毒(HIV)Tat调节体内反式激活,诱导保护淋巴母细胞CEM-SS细胞免受HIV(IIIB株)杀伤,并抑制五种HIV-1株(WM,MN,VS,JR-CSF,和丝裂原刺激的外周血单核细胞中的III(B)),均呈剂量依赖性。 Mal.4在体外抑制基础转录和Tat调控的反式激活。 Mal.4的靶标已定位到HIV长末端重复序列的核苷酸-87至-40,Mal.4直接特异性地干扰了Spl与HIV长末端重复序列中Spl位点的结合,通过抑制前病毒表达, Mal.4可能能够打断HIV感染患者的野生型和逆转录酶或蛋白酶突变病毒的生命周期。 [参考:29]

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