Endonuclease Regnase‐1/Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1) in controlling immune responses and beyond

The activation of inflammatory cells is controlled at transcriptional and posttranscriptional levels. Posttranscriptional regulation modifies mRNA stability and translation, allowing for elaborate control of proteins required for inflammation, such as proinflammatory cytokines, prostaglandin synthas...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Wiley interdisciplinary reviews. RNA 2018-01, Vol.9 (1), p.e1449-n/a
1. Verfasser: Takeuchi, Osamu
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page n/a
container_issue 1
container_start_page e1449
container_title Wiley interdisciplinary reviews. RNA
container_volume 9
creator Takeuchi, Osamu
description The activation of inflammatory cells is controlled at transcriptional and posttranscriptional levels. Posttranscriptional regulation modifies mRNA stability and translation, allowing for elaborate control of proteins required for inflammation, such as proinflammatory cytokines, prostaglandin synthases, cell surface co‐stimulatory molecules, and even transcriptional modifiers. Such regulation is important for coordinating the initiation and resolution of inflammation, and is mediated by a set of RNA‐binding proteins (RBPs), including Regnase‐1, Roquin, Tristetraprolin (TTP), and AU‐rich elements/poly(U)‐binding/degradation factor 1 (AUF1). Among these, Regnase‐1, also known as Zc3h12a and Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1), acts as an endoribonuclease responsible for the degradation of mRNAs involved in inflammatory responses. Conversely, the RBPs Roquin and TTP trigger exonucleolytic degradation of mRNAs by recruiting the CCR4‐NOT deadenylase complex. Regnase‐1 specifically recognizes stem‐loop structures present in 3′‐untranslated regions of cytokine mRNAs, and directly degrades the mRNAs in a translation‐ and ATP‐dependent RNA helicase upframeshift 1 (UPF1)‐dependent manner that is reminiscent of nonsense‐mediated decay. Regnase‐1 regulates the activation of innate and acquired immune cells, and is critical for maintaining immune homeostasis as well as preventing over‐activation of the immune system under inflammatory conditions. Furthermore, recent studies have revealed that Regnase‐1 and its family members are involved not only in immunity but also in various biological processes. In this article, I review molecular mechanisms of Regnase‐1‐mediated mRNA decay and its physiological roles. WIREs RNA 2018, 9:e1449. doi: 10.1002/wrna.1449 This article is categorized under: RNA Interactions with Proteins and Other Molecules > Protein–RNA Interactions: Functional Implications RNA Turnover and Surveillance > Regulation of RNA Stability RNA in Disease and Development > RNA in Disease Regnase‐1/MCPIP1 is an endoribonuclease that degrades a set of mRNAs in a translation dependent manner by interacting with UPF1. Regnase‐1 recognizes mRNAs harboring a stem‐loop structure in the 3' untranslated region, and regulates various biological processes such as innate and adaptive immunity, as well as development, cancer and metabolism.
doi_str_mv 10.1002/wrna.1449
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1941090907</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1941090907</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3499-a010a1eb36afc636e2a05591881a1e2952753497096856253f613331e9b17a623</originalsourceid><addsrcrecordid>eNp10c1KxDAQB_Agiop68AUk4EUP62aStmmOsqwf4BeieCzZdFYjbbI2LbI3wRfwGX0SU1dFBBPChOHHn5AhZBvYATDGh8-N0weQJGqJrINM5UAy4Ms_d5aska0QHllcCeMSYJWs8VxxlXG-Tl7HrvSuMxXqgPQa712s7y9vMDz3zpt5i9Q8YO1bbVpr6KzxLVrXg3isKzuD5e8u3TsfXZ1ewT61jhrv2sZXlXX31NZ155A2GGbeBQxUu5JOcO5duUlWproKuPVVN8jt0fhmdDI4uzw-HR2eDYxIlBpoBkwDTkSmpyYTGXLN0lRBnkNsc5VymUYomcryNOOpmGYghABUE5A642KD7C1y43ufOgxtUdtgsKq0Q9-FAlQCTMUtI939Qx99Fz-66pVUAErkIqr9hTKND6HBaTFrbK2beQGs6IdT9MMp-uFEu_OV2E1qLH_k9ygiGC7As61w_n9ScXd9cfgZ-QEh75uG</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1979119383</pqid></control><display><type>article</type><title>Endonuclease Regnase‐1/Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1) in controlling immune responses and beyond</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Takeuchi, Osamu</creator><creatorcontrib>Takeuchi, Osamu</creatorcontrib><description>The activation of inflammatory cells is controlled at transcriptional and posttranscriptional levels. Posttranscriptional regulation modifies mRNA stability and translation, allowing for elaborate control of proteins required for inflammation, such as proinflammatory cytokines, prostaglandin synthases, cell surface co‐stimulatory molecules, and even transcriptional modifiers. Such regulation is important for coordinating the initiation and resolution of inflammation, and is mediated by a set of RNA‐binding proteins (RBPs), including Regnase‐1, Roquin, Tristetraprolin (TTP), and AU‐rich elements/poly(U)‐binding/degradation factor 1 (AUF1). Among these, Regnase‐1, also known as Zc3h12a and Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1), acts as an endoribonuclease responsible for the degradation of mRNAs involved in inflammatory responses. Conversely, the RBPs Roquin and TTP trigger exonucleolytic degradation of mRNAs by recruiting the CCR4‐NOT deadenylase complex. Regnase‐1 specifically recognizes stem‐loop structures present in 3′‐untranslated regions of cytokine mRNAs, and directly degrades the mRNAs in a translation‐ and ATP‐dependent RNA helicase upframeshift 1 (UPF1)‐dependent manner that is reminiscent of nonsense‐mediated decay. Regnase‐1 regulates the activation of innate and acquired immune cells, and is critical for maintaining immune homeostasis as well as preventing over‐activation of the immune system under inflammatory conditions. Furthermore, recent studies have revealed that Regnase‐1 and its family members are involved not only in immunity but also in various biological processes. In this article, I review molecular mechanisms of Regnase‐1‐mediated mRNA decay and its physiological roles. WIREs RNA 2018, 9:e1449. doi: 10.1002/wrna.1449 This article is categorized under: RNA Interactions with Proteins and Other Molecules &gt; Protein–RNA Interactions: Functional Implications RNA Turnover and Surveillance &gt; Regulation of RNA Stability RNA in Disease and Development &gt; RNA in Disease Regnase‐1/MCPIP1 is an endoribonuclease that degrades a set of mRNAs in a translation dependent manner by interacting with UPF1. Regnase‐1 recognizes mRNAs harboring a stem‐loop structure in the 3' untranslated region, and regulates various biological processes such as innate and adaptive immunity, as well as development, cancer and metabolism.</description><identifier>ISSN: 1757-7004</identifier><identifier>EISSN: 1757-7012</identifier><identifier>DOI: 10.1002/wrna.1449</identifier><identifier>PMID: 28929622</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley &amp; Sons, Inc</publisher><subject>3' Untranslated regions ; Cell surface ; Cytokines ; DNA helicase ; Endonuclease ; Gene regulation ; Homeostasis ; Immune response ; Immune system ; Inflammation ; Molecular modelling ; Monocyte chemoattractant protein 1 ; mRNA stability ; mRNA turnover ; Post-transcription ; Proteins ; RNA helicase ; RNA-binding protein ; Translation</subject><ispartof>Wiley interdisciplinary reviews. RNA, 2018-01, Vol.9 (1), p.e1449-n/a</ispartof><rights>2017 Wiley Periodicals, Inc.</rights><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3499-a010a1eb36afc636e2a05591881a1e2952753497096856253f613331e9b17a623</citedby><cites>FETCH-LOGICAL-c3499-a010a1eb36afc636e2a05591881a1e2952753497096856253f613331e9b17a623</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fwrna.1449$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fwrna.1449$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28929622$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeuchi, Osamu</creatorcontrib><title>Endonuclease Regnase‐1/Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1) in controlling immune responses and beyond</title><title>Wiley interdisciplinary reviews. RNA</title><addtitle>Wiley Interdiscip Rev RNA</addtitle><description>The activation of inflammatory cells is controlled at transcriptional and posttranscriptional levels. Posttranscriptional regulation modifies mRNA stability and translation, allowing for elaborate control of proteins required for inflammation, such as proinflammatory cytokines, prostaglandin synthases, cell surface co‐stimulatory molecules, and even transcriptional modifiers. Such regulation is important for coordinating the initiation and resolution of inflammation, and is mediated by a set of RNA‐binding proteins (RBPs), including Regnase‐1, Roquin, Tristetraprolin (TTP), and AU‐rich elements/poly(U)‐binding/degradation factor 1 (AUF1). Among these, Regnase‐1, also known as Zc3h12a and Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1), acts as an endoribonuclease responsible for the degradation of mRNAs involved in inflammatory responses. Conversely, the RBPs Roquin and TTP trigger exonucleolytic degradation of mRNAs by recruiting the CCR4‐NOT deadenylase complex. Regnase‐1 specifically recognizes stem‐loop structures present in 3′‐untranslated regions of cytokine mRNAs, and directly degrades the mRNAs in a translation‐ and ATP‐dependent RNA helicase upframeshift 1 (UPF1)‐dependent manner that is reminiscent of nonsense‐mediated decay. Regnase‐1 regulates the activation of innate and acquired immune cells, and is critical for maintaining immune homeostasis as well as preventing over‐activation of the immune system under inflammatory conditions. Furthermore, recent studies have revealed that Regnase‐1 and its family members are involved not only in immunity but also in various biological processes. In this article, I review molecular mechanisms of Regnase‐1‐mediated mRNA decay and its physiological roles. WIREs RNA 2018, 9:e1449. doi: 10.1002/wrna.1449 This article is categorized under: RNA Interactions with Proteins and Other Molecules &gt; Protein–RNA Interactions: Functional Implications RNA Turnover and Surveillance &gt; Regulation of RNA Stability RNA in Disease and Development &gt; RNA in Disease Regnase‐1/MCPIP1 is an endoribonuclease that degrades a set of mRNAs in a translation dependent manner by interacting with UPF1. Regnase‐1 recognizes mRNAs harboring a stem‐loop structure in the 3' untranslated region, and regulates various biological processes such as innate and adaptive immunity, as well as development, cancer and metabolism.</description><subject>3' Untranslated regions</subject><subject>Cell surface</subject><subject>Cytokines</subject><subject>DNA helicase</subject><subject>Endonuclease</subject><subject>Gene regulation</subject><subject>Homeostasis</subject><subject>Immune response</subject><subject>Immune system</subject><subject>Inflammation</subject><subject>Molecular modelling</subject><subject>Monocyte chemoattractant protein 1</subject><subject>mRNA stability</subject><subject>mRNA turnover</subject><subject>Post-transcription</subject><subject>Proteins</subject><subject>RNA helicase</subject><subject>RNA-binding protein</subject><subject>Translation</subject><issn>1757-7004</issn><issn>1757-7012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp10c1KxDAQB_Agiop68AUk4EUP62aStmmOsqwf4BeieCzZdFYjbbI2LbI3wRfwGX0SU1dFBBPChOHHn5AhZBvYATDGh8-N0weQJGqJrINM5UAy4Ms_d5aska0QHllcCeMSYJWs8VxxlXG-Tl7HrvSuMxXqgPQa712s7y9vMDz3zpt5i9Q8YO1bbVpr6KzxLVrXg3isKzuD5e8u3TsfXZ1ewT61jhrv2sZXlXX31NZ155A2GGbeBQxUu5JOcO5duUlWproKuPVVN8jt0fhmdDI4uzw-HR2eDYxIlBpoBkwDTkSmpyYTGXLN0lRBnkNsc5VymUYomcryNOOpmGYghABUE5A642KD7C1y43ufOgxtUdtgsKq0Q9-FAlQCTMUtI939Qx99Fz-66pVUAErkIqr9hTKND6HBaTFrbK2beQGs6IdT9MMp-uFEu_OV2E1qLH_k9ygiGC7As61w_n9ScXd9cfgZ-QEh75uG</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Takeuchi, Osamu</creator><general>John Wiley &amp; Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TM</scope><scope>7X8</scope></search><sort><creationdate>201801</creationdate><title>Endonuclease Regnase‐1/Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1) in controlling immune responses and beyond</title><author>Takeuchi, Osamu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3499-a010a1eb36afc636e2a05591881a1e2952753497096856253f613331e9b17a623</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>3' Untranslated regions</topic><topic>Cell surface</topic><topic>Cytokines</topic><topic>DNA helicase</topic><topic>Endonuclease</topic><topic>Gene regulation</topic><topic>Homeostasis</topic><topic>Immune response</topic><topic>Immune system</topic><topic>Inflammation</topic><topic>Molecular modelling</topic><topic>Monocyte chemoattractant protein 1</topic><topic>mRNA stability</topic><topic>mRNA turnover</topic><topic>Post-transcription</topic><topic>Proteins</topic><topic>RNA helicase</topic><topic>RNA-binding protein</topic><topic>Translation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Takeuchi, Osamu</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Wiley interdisciplinary reviews. RNA</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeuchi, Osamu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Endonuclease Regnase‐1/Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1) in controlling immune responses and beyond</atitle><jtitle>Wiley interdisciplinary reviews. RNA</jtitle><addtitle>Wiley Interdiscip Rev RNA</addtitle><date>2018-01</date><risdate>2018</risdate><volume>9</volume><issue>1</issue><spage>e1449</spage><epage>n/a</epage><pages>e1449-n/a</pages><issn>1757-7004</issn><eissn>1757-7012</eissn><abstract>The activation of inflammatory cells is controlled at transcriptional and posttranscriptional levels. Posttranscriptional regulation modifies mRNA stability and translation, allowing for elaborate control of proteins required for inflammation, such as proinflammatory cytokines, prostaglandin synthases, cell surface co‐stimulatory molecules, and even transcriptional modifiers. Such regulation is important for coordinating the initiation and resolution of inflammation, and is mediated by a set of RNA‐binding proteins (RBPs), including Regnase‐1, Roquin, Tristetraprolin (TTP), and AU‐rich elements/poly(U)‐binding/degradation factor 1 (AUF1). Among these, Regnase‐1, also known as Zc3h12a and Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1), acts as an endoribonuclease responsible for the degradation of mRNAs involved in inflammatory responses. Conversely, the RBPs Roquin and TTP trigger exonucleolytic degradation of mRNAs by recruiting the CCR4‐NOT deadenylase complex. Regnase‐1 specifically recognizes stem‐loop structures present in 3′‐untranslated regions of cytokine mRNAs, and directly degrades the mRNAs in a translation‐ and ATP‐dependent RNA helicase upframeshift 1 (UPF1)‐dependent manner that is reminiscent of nonsense‐mediated decay. Regnase‐1 regulates the activation of innate and acquired immune cells, and is critical for maintaining immune homeostasis as well as preventing over‐activation of the immune system under inflammatory conditions. Furthermore, recent studies have revealed that Regnase‐1 and its family members are involved not only in immunity but also in various biological processes. In this article, I review molecular mechanisms of Regnase‐1‐mediated mRNA decay and its physiological roles. WIREs RNA 2018, 9:e1449. doi: 10.1002/wrna.1449 This article is categorized under: RNA Interactions with Proteins and Other Molecules &gt; Protein–RNA Interactions: Functional Implications RNA Turnover and Surveillance &gt; Regulation of RNA Stability RNA in Disease and Development &gt; RNA in Disease Regnase‐1/MCPIP1 is an endoribonuclease that degrades a set of mRNAs in a translation dependent manner by interacting with UPF1. Regnase‐1 recognizes mRNAs harboring a stem‐loop structure in the 3' untranslated region, and regulates various biological processes such as innate and adaptive immunity, as well as development, cancer and metabolism.</abstract><cop>Hoboken, USA</cop><pub>John Wiley &amp; Sons, Inc</pub><pmid>28929622</pmid><doi>10.1002/wrna.1449</doi><tpages>14</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1757-7004
ispartof Wiley interdisciplinary reviews. RNA, 2018-01, Vol.9 (1), p.e1449-n/a
issn 1757-7004
1757-7012
language eng
recordid cdi_proquest_miscellaneous_1941090907
source Wiley Online Library Journals Frontfile Complete
subjects 3' Untranslated regions
Cell surface
Cytokines
DNA helicase
Endonuclease
Gene regulation
Homeostasis
Immune response
Immune system
Inflammation
Molecular modelling
Monocyte chemoattractant protein 1
mRNA stability
mRNA turnover
Post-transcription
Proteins
RNA helicase
RNA-binding protein
Translation
title Endonuclease Regnase‐1/Monocyte chemotactic protein‐1‐induced protein‐1 (MCPIP1) in controlling immune responses and beyond
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-19T04%3A53%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Endonuclease%20Regnase%E2%80%901/Monocyte%20chemotactic%20protein%E2%80%901%E2%80%90induced%20protein%E2%80%901%20(MCPIP1)%20in%20controlling%20immune%20responses%20and%20beyond&rft.jtitle=Wiley%20interdisciplinary%20reviews.%20RNA&rft.au=Takeuchi,%20Osamu&rft.date=2018-01&rft.volume=9&rft.issue=1&rft.spage=e1449&rft.epage=n/a&rft.pages=e1449-n/a&rft.issn=1757-7004&rft.eissn=1757-7012&rft_id=info:doi/10.1002/wrna.1449&rft_dat=%3Cproquest_cross%3E1941090907%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1979119383&rft_id=info:pmid/28929622&rfr_iscdi=true