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影响mRNA周转和翻译的RNA结合蛋白的组织和年龄依赖性表达。

Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation.

作者信息

Masuda Kiyoshi, Marasa Bernard, Martindale Jennifer L, Halushka Marc K, Gorospe Myriam

机构信息

Laboratory of Cellular and Molecular Biology, NIA-IRP, NIH, Baltimore, MD 21224, USA.

出版信息

Aging (Albany NY). 2009 Jul 26;1(8):681-98. doi: 10.18632/aging.100073.

Abstract

Gene expression patterns vary dramatically in a tissue-specific and age-dependent manner. RNA-binding proteins that regulate mRNA turnover and/or translation (TTR-RBPs) critically affect the subsets of expressed proteins. However, very little is known regarding the tissue- and age-dependent expression of TTR-RBPs in humans. Here, we use human tissue arrays containing a panel of organ biopsies from donors of different ages, to study the distribution and abundance of four TTR-RBPs: HuR, AUF1, TIA-1, and TTP. HuR and AUF1 were expressed with remarkably similar patterns. Both TTR-RBPs were present in high percentages of cells and displayed elevated intensities in many age groups and tissues, most notably in the gastrointestinal and reproductive systems; they were moderately expressed in the urinary and immune systems, and were almost undetectable in muscle and brain. TIA-1 was also abundant in many tissues and age groups; TIA-1 was expressed at high levels in the gastrointestinal, immune, urinary, and reproductive systems, and at low levels in brain and muscle. By contrast, TTP-expressing cells, as well as TTP signal intensities declined with advancing age, particularly in the immune, nervous, and muscular systems; however, TTP levels remained elevated in the gastrointestinal tract. The widespread abundance of HuR, AUF1, and TIA-1 throughout the body and in all age groups was in stark contrast with their declining levels in human diploid fibroblasts (HDFs) undergoing replicative senescence, a cultured-cell model of aging. Conversely, TTP levels increased in senescent HDFs, while TTP levels decreased with advancing age. Our studies provide a framework for the study of human TTR-RBP function in different tissues, throughout the human life span.

摘要

基因表达模式以组织特异性和年龄依赖性的方式显著变化。调节mRNA周转和/或翻译的RNA结合蛋白(TTR-RBP)对所表达蛋白质的亚群有至关重要的影响。然而,关于人类中TTR-RBP的组织和年龄依赖性表达,我们了解得非常少。在这里,我们使用包含来自不同年龄供体的一组器官活检的人体组织阵列,来研究四种TTR-RBP:HuR、AUF1、TIA-1和TTP的分布和丰度。HuR和AUF1以非常相似的模式表达。这两种TTR-RBP在高比例的细胞中存在,并且在许多年龄组和组织中显示出增强的强度,最显著的是在胃肠道和生殖系统中;它们在泌尿系统和免疫系统中适度表达,而在肌肉和大脑中几乎检测不到。TIA-1在许多组织和年龄组中也很丰富;TIA-1在胃肠道、免疫系统、泌尿系统和生殖系统中高水平表达,而在大脑和肌肉中低水平表达。相比之下,随着年龄的增长,表达TTP的细胞以及TTP信号强度下降,特别是在免疫系统、神经系统和肌肉系统中;然而,TTP水平在胃肠道中仍然升高。HuR、AUF1和TIA-1在全身和所有年龄组中的广泛丰富与它们在经历复制性衰老的人类二倍体成纤维细胞(HDF)中的下降水平形成鲜明对比,HDF是一种衰老的培养细胞模型。相反,衰老的HDF中TTP水平增加,而随着年龄的增长TTP水平下降。我们的研究为研究人类整个生命周期中不同组织中TTR-RBP的功能提供了一个框架。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d516/2806049/2428902f3e4b/aging-01-681-g001.jpg

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