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

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 expressi...

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Autores principales: Masuda, Kiyoshi, Marasa, Bernard, Martindale, Jennifer L., Halushka, Marc K., Gorospe, Myriam
Formato: Texto
Lenguaje:English
Publicado: Impact Journals LLC 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806049/
https://www.ncbi.nlm.nih.gov/pubmed/20157551
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author Masuda, Kiyoshi
Marasa, Bernard
Martindale, Jennifer L.
Halushka, Marc K.
Gorospe, Myriam
author_facet Masuda, Kiyoshi
Marasa, Bernard
Martindale, Jennifer L.
Halushka, Marc K.
Gorospe, Myriam
author_sort Masuda, Kiyoshi
collection PubMed
description 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.
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spelling pubmed-28060492010-02-12 Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation Masuda, Kiyoshi Marasa, Bernard Martindale, Jennifer L. Halushka, Marc K. Gorospe, Myriam Aging (Albany NY) Priority Research Paper 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. Impact Journals LLC 2009-07-26 /pmc/articles/PMC2806049/ /pubmed/20157551 Text en Copyright: ©2009 Masuda et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Priority Research Paper
Masuda, Kiyoshi
Marasa, Bernard
Martindale, Jennifer L.
Halushka, Marc K.
Gorospe, Myriam
Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation
title Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation
title_full Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation
title_fullStr Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation
title_full_unstemmed Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation
title_short Tissue- and age-dependent expression of RNA-binding proteins that influence mRNA turnover and translation
title_sort tissue- and age-dependent expression of rna-binding proteins that influence mrna turnover and translation
topic Priority Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806049/
https://www.ncbi.nlm.nih.gov/pubmed/20157551
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