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首页> 外文期刊>Human Molecular Genetics >Primary non-random X inactivation associated with disruption of Xist promoter regulation.
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Primary non-random X inactivation associated with disruption of Xist promoter regulation.

机译:原发性非随机性X失活与Xist启动子调控的破坏有关。

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摘要

In this report we demonstrate primary non-random X chromosome inactivation following targeted mutagenesis of a region immediately upstream of XIST promoter P(1). In heterozygous animals there is a preferential inactivation of the targeted X chromosome in 80--90% of cells. The phenotype correlates with inappropriate activation of XIST in a proportion of the mutant XY embryonic stem cells. Strand-specific analysis revealed increased sense transcription initiating upstream of XIST promoter P(1). There was, however, no discernible effect on transcription from the antisense Tsix gene. We demonstrate that the in vitro and in vivo phenotypes are specifically attributable to the presence of a PGKneo cassette at the targeted locus. These findings are discussed in the context of understanding mechanisms of XIST gene regulation in X inactivation.
机译:在此报告中,我们证明了XIST启动子P(1)上游区域的定向诱变后,主要的非随机X染色体失活。在杂合动物中,目标X染色体在80--90%的细胞中优先失活。该表型与一部分突变的XY胚胎干细胞中XIST的不适当激活相关。链特异性分析显示XIST启动子P(1)上游启动的有义转录增加。然而,对来自反义Tsix基因的转录没有明显的影响。我们证明了体外和体内的表型是具体归因于在目标位置的PGKneo盒的存在。在了解X灭活过程中XIST基因调控机制的背景下讨论了这些发现。

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