首页> 美国卫生研究院文献>Journal of Virology >Transcriptional silencing of human immunodeficiency virus type 1 long terminal repeat-driven gene expression by the Krüppel-associated box repressor domain targeted to the transactivating response element.
【2h】

Transcriptional silencing of human immunodeficiency virus type 1 long terminal repeat-driven gene expression by the Krüppel-associated box repressor domain targeted to the transactivating response element.

机译:人类免疫缺陷病毒1型长末端重复驱动基因表达的转录沉默,该转录是通过与反转录激活元件相关的Krüppel相关盒阻遏物域实现的。

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

The evolutionarily conserved protein domain, called the Krüppel-associated box (KRAB), present in the amino termini of a large number of Krüppel-type zinc finger proteins is a strong repressor domain. In order to develop novel strategies to control human immunodeficiency virus type 1 (HIV-1) gene expression, we constructed a series of expression vectors expressing the wild-type Tat or Tat transdominant negative mutants fused to the KRAB repressor domain. We found that the KRAB domain tethered to the transactivating response element is able to suppress both basal and Tat-mediated activity of HIV-1 long terminal repeat-driven gene expression. These results suggest that the KRAB repressor domain fused to the Tat transdominant negative mutants can be successfully employed to control HIV-1 gene expression.
机译:存在于大量Krüppel型锌指蛋白氨基末端的进化上保守的蛋白质结构域称为Krüppel相关盒(KRAB),是一个强大的阻遏域。为了开发新的策略来控制人类免疫缺陷病毒1型(HIV-1)基因表达,我们构建了一系列表达载体,表达与KRAB阻遏物结构域融合的野生型Tat或Tat转化性负突变体。我们发现绑定到反式激活元件的KRAB域能够抑制HIV-1长末端重复驱动基因表达的基础和Tat介导的活性。这些结果表明,融合到Tat显性负突变体上的KRAB阻遏物结构域可以成功地用于控制HIV-1基因的表达。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号