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人正常组织和癌细胞系中Tristetraprolin(TTP)家族成员转录本的表达比较

Comparative expression of tristetraprolin (TTP) family member transcripts in normal human tissues and cancer cell lines.

作者信息

Carrick Danielle M, Blackshear Perry J

机构信息

The Office of Clinical Research, National Institute of Environmental Health Sciences, NIEHS MD A2-05, 111 Alexander Drive, Research Triangle Park, NC 27709, USA.

出版信息

Arch Biochem Biophys. 2007 Jun 15;462(2):278-85. doi: 10.1016/j.abb.2007.04.011. Epub 2007 Apr 26.

Abstract

The tristetraprolin (TTP) family of tandem zinc finger proteins comprises three members in man and most other mammals, with a fourth expressed in rodents. In mice, gene disruption of TTP itself leads to a systemic inflammatory syndrome that is mediated in large part by over-expression of tumor necrosis factor alpha (TNF). This increased expression is secondary to stabilization of the TNF mRNA in the TTP KO mice, a finding that led to the characterization of TTP as an mRNA binding protein that can promote the removal of the poly(A) tail from selected mRNAs and facilitate their nucleolytic destruction. The other human family members behave similarly to TTP in over-expression studies of transfected cells, but gene disruption experiments have implicated them in different physiological processes. In the present study, we developed a real-time PCR assay for all three human family members that allowed for comparative measurements of all three family members in the same tissues and cells. We used this assay to quantitate expression levels of all three transcripts in a variety of normal human tissues, as well as in the ;;NCI 60", a well characterized panel of human tumor cell lines. Although studies in fibroblasts and macrophages derived from knockout mice have failed to demonstrate compensatory expression of the family members in terms of transcript levels, it remains possible that the different family members can function as ;;TTP equivalents" in certain physiological or pathological circumstances.

摘要

串联锌指蛋白的Tristetraprolin(TTP)家族在人类和大多数其他哺乳动物中包含三个成员,在啮齿动物中表达第四个成员。在小鼠中,TTP自身的基因破坏会导致一种全身性炎症综合征,这在很大程度上是由肿瘤坏死因子α(TNF)的过度表达介导的。这种表达增加是由于TTP基因敲除小鼠中TNF mRNA的稳定性增加,这一发现导致TTP被鉴定为一种mRNA结合蛋白,它可以促进从选定的mRNA上去除多聚(A)尾巴并促进其核酸酶降解。在转染细胞的过表达研究中,其他人类家族成员的行为与TTP相似,但基因破坏实验表明它们参与了不同的生理过程。在本研究中,我们开发了一种针对所有三个人类家族成员的实时PCR检测方法,该方法允许在同一组织和细胞中对所有三个家族成员进行比较测量。我们使用该检测方法来定量所有三种转录本在各种正常人类组织以及“NCI 60”(一组特征明确的人类肿瘤细胞系)中的表达水平。尽管对来自基因敲除小鼠的成纤维细胞和巨噬细胞的研究未能在转录水平上证明家族成员的代偿性表达,但在某些生理或病理情况下,不同的家族成员仍有可能作为“TTP等效物”发挥作用。

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