Role of Auf1 in elimination of oxidatively damaged messenger RNA in human cells
In aerobically growing cells, in which reactive oxygen species are produced, the guanine base of RNA is oxidized to 8-oxo-7,8-dihydroguanine, which induces alterations in gene expression. Here we show that the human Auf1 protein, also called HNRNPD, binds specifically to RNA containing this oxidized...
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creator | Ishii, Takashi Hayakawa, Hiroshi Sekiguchi, Takeshi Adachi, Noritaka Sekiguchi, Mutsuo |
description | In aerobically growing cells, in which reactive oxygen species are produced, the guanine base of RNA is oxidized to 8-oxo-7,8-dihydroguanine, which induces alterations in gene expression. Here we show that the human Auf1 protein, also called HNRNPD, binds specifically to RNA containing this oxidized base and may be involved in cellular processes associated with managing the problems caused by RNA oxidation. Auf1-deficient cells were constructed from human HeLa and Nalm-6 lines using two different targeting procedures. Both types of Auf1-deficient cells are viable, but exhibit growth retardation. The stability of messenger RNA for four different housekeeping genes was determined in Auf1-deficient and -proficient cells, treated with or without hydrogen peroxide. The level of oxidized messenger RNA was considerably higher in Auf1-deficient cells than in Auf1-proficient cells. Auf1 may play a role in the elimination of oxidized RNA, which is required for the maintenance of proper gene expression under conditions of oxidative stress.
•The human Auf1 protein binds specifically to RNA carrying 8-oxo-7,8-dihydroguanine.•Oxidized mRNA is more rapidly degraded than is normal mRNA.•The selective degradation of oxidized mRNA is considerably lower in Auf1−/− cells.•Auf1−/− cells are viable, but exhibit growth retardation. |
doi_str_mv | 10.1016/j.freeradbiomed.2014.11.018 |
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•The human Auf1 protein binds specifically to RNA carrying 8-oxo-7,8-dihydroguanine.•Oxidized mRNA is more rapidly degraded than is normal mRNA.•The selective degradation of oxidized mRNA is considerably lower in Auf1−/− cells.•Auf1−/− cells are viable, but exhibit growth retardation.</description><identifier>ISSN: 0891-5849</identifier><identifier>EISSN: 1873-4596</identifier><identifier>DOI: 10.1016/j.freeradbiomed.2014.11.018</identifier><identifier>PMID: 25486179</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>8-Oxo-7,8-dihydroguanine ; Auf1 protein ; Cell Line ; Free radicals ; Heterogeneous-Nuclear Ribonucleoprotein D - physiology ; Humans ; Oxidative Stress ; Oxidized RNA ; RNA degradation ; RNA, Messenger - metabolism</subject><ispartof>Free radical biology & medicine, 2015-02, Vol.79, p.109-116</ispartof><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c449t-9ac24e8276a1f5652618be1c1d0b79fae789751e231f12dc25fb4a1eb8b7cc0c3</citedby><cites>FETCH-LOGICAL-c449t-9ac24e8276a1f5652618be1c1d0b79fae789751e231f12dc25fb4a1eb8b7cc0c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.freeradbiomed.2014.11.018$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25486179$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ishii, Takashi</creatorcontrib><creatorcontrib>Hayakawa, Hiroshi</creatorcontrib><creatorcontrib>Sekiguchi, Takeshi</creatorcontrib><creatorcontrib>Adachi, Noritaka</creatorcontrib><creatorcontrib>Sekiguchi, Mutsuo</creatorcontrib><title>Role of Auf1 in elimination of oxidatively damaged messenger RNA in human cells</title><title>Free radical biology & medicine</title><addtitle>Free Radic Biol Med</addtitle><description>In aerobically growing cells, in which reactive oxygen species are produced, the guanine base of RNA is oxidized to 8-oxo-7,8-dihydroguanine, which induces alterations in gene expression. Here we show that the human Auf1 protein, also called HNRNPD, binds specifically to RNA containing this oxidized base and may be involved in cellular processes associated with managing the problems caused by RNA oxidation. Auf1-deficient cells were constructed from human HeLa and Nalm-6 lines using two different targeting procedures. Both types of Auf1-deficient cells are viable, but exhibit growth retardation. The stability of messenger RNA for four different housekeeping genes was determined in Auf1-deficient and -proficient cells, treated with or without hydrogen peroxide. The level of oxidized messenger RNA was considerably higher in Auf1-deficient cells than in Auf1-proficient cells. Auf1 may play a role in the elimination of oxidized RNA, which is required for the maintenance of proper gene expression under conditions of oxidative stress.
•The human Auf1 protein binds specifically to RNA carrying 8-oxo-7,8-dihydroguanine.•Oxidized mRNA is more rapidly degraded than is normal mRNA.•The selective degradation of oxidized mRNA is considerably lower in Auf1−/− cells.•Auf1−/− cells are viable, but exhibit growth retardation.</description><subject>8-Oxo-7,8-dihydroguanine</subject><subject>Auf1 protein</subject><subject>Cell Line</subject><subject>Free radicals</subject><subject>Heterogeneous-Nuclear Ribonucleoprotein D - physiology</subject><subject>Humans</subject><subject>Oxidative Stress</subject><subject>Oxidized RNA</subject><subject>RNA degradation</subject><subject>RNA, Messenger - metabolism</subject><issn>0891-5849</issn><issn>1873-4596</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE1LxDAQhoMo7rr6F6TgxUtrppu0KZ4W8QsWF0TPIU0mmqVt1mQr-u9tWffgzdMwM-87Hw8hF0AzoFBcrTMbEIMytfMtmiynwDKAjII4IFMQ5TxlvCoOyZSKClIuWDUhJzGuKaWMz8UxmeSciQLKakpWz77BxNtk0VtIXJdg41rXqa3z3Vj2X84MySc234lRrXpDk7QYI3ZvGJLnp8Xoee9b1SUamyaekiOrmohnv3FGXu9uX24e0uXq_vFmsUw1Y9U2rZTOGYq8LBRYXvC8AFEjaDC0LiursBRVyQHzOVjIjc65rZkCrEVdak31fEYud3M3wX_0GLeydXG8QHXo-yihGP6GArgYpNc7qQ4-xoBWboJrVfiWQOVIVK7lH6JyJCoB5EB0cJ__Lurrsbf37hEOgtudAId3Px0GGbXDTqNxAfVWGu_-tegHxSeOyQ</recordid><startdate>20150201</startdate><enddate>20150201</enddate><creator>Ishii, Takashi</creator><creator>Hayakawa, Hiroshi</creator><creator>Sekiguchi, Takeshi</creator><creator>Adachi, Noritaka</creator><creator>Sekiguchi, Mutsuo</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150201</creationdate><title>Role of Auf1 in elimination of oxidatively damaged messenger RNA in human cells</title><author>Ishii, Takashi ; Hayakawa, Hiroshi ; Sekiguchi, Takeshi ; Adachi, Noritaka ; Sekiguchi, Mutsuo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c449t-9ac24e8276a1f5652618be1c1d0b79fae789751e231f12dc25fb4a1eb8b7cc0c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>8-Oxo-7,8-dihydroguanine</topic><topic>Auf1 protein</topic><topic>Cell Line</topic><topic>Free radicals</topic><topic>Heterogeneous-Nuclear Ribonucleoprotein D - physiology</topic><topic>Humans</topic><topic>Oxidative Stress</topic><topic>Oxidized RNA</topic><topic>RNA degradation</topic><topic>RNA, Messenger - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ishii, Takashi</creatorcontrib><creatorcontrib>Hayakawa, Hiroshi</creatorcontrib><creatorcontrib>Sekiguchi, Takeshi</creatorcontrib><creatorcontrib>Adachi, Noritaka</creatorcontrib><creatorcontrib>Sekiguchi, Mutsuo</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Free radical biology & medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ishii, Takashi</au><au>Hayakawa, Hiroshi</au><au>Sekiguchi, Takeshi</au><au>Adachi, Noritaka</au><au>Sekiguchi, Mutsuo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Auf1 in elimination of oxidatively damaged messenger RNA in human cells</atitle><jtitle>Free radical biology & medicine</jtitle><addtitle>Free Radic Biol Med</addtitle><date>2015-02-01</date><risdate>2015</risdate><volume>79</volume><spage>109</spage><epage>116</epage><pages>109-116</pages><issn>0891-5849</issn><eissn>1873-4596</eissn><abstract>In aerobically growing cells, in which reactive oxygen species are produced, the guanine base of RNA is oxidized to 8-oxo-7,8-dihydroguanine, which induces alterations in gene expression. Here we show that the human Auf1 protein, also called HNRNPD, binds specifically to RNA containing this oxidized base and may be involved in cellular processes associated with managing the problems caused by RNA oxidation. Auf1-deficient cells were constructed from human HeLa and Nalm-6 lines using two different targeting procedures. Both types of Auf1-deficient cells are viable, but exhibit growth retardation. The stability of messenger RNA for four different housekeeping genes was determined in Auf1-deficient and -proficient cells, treated with or without hydrogen peroxide. The level of oxidized messenger RNA was considerably higher in Auf1-deficient cells than in Auf1-proficient cells. Auf1 may play a role in the elimination of oxidized RNA, which is required for the maintenance of proper gene expression under conditions of oxidative stress.
•The human Auf1 protein binds specifically to RNA carrying 8-oxo-7,8-dihydroguanine.•Oxidized mRNA is more rapidly degraded than is normal mRNA.•The selective degradation of oxidized mRNA is considerably lower in Auf1−/− cells.•Auf1−/− cells are viable, but exhibit growth retardation.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>25486179</pmid><doi>10.1016/j.freeradbiomed.2014.11.018</doi><tpages>8</tpages></addata></record> |
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subjects | 8-Oxo-7,8-dihydroguanine Auf1 protein Cell Line Free radicals Heterogeneous-Nuclear Ribonucleoprotein D - physiology Humans Oxidative Stress Oxidized RNA RNA degradation RNA, Messenger - metabolism |
title | Role of Auf1 in elimination of oxidatively damaged messenger RNA in human cells |
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