Ordered structure-forming properties of the intrinsically disordered AB region of hRXRγ and its ability to promote liquid-liquid phase separation
•We describe the biochemical and biophysical properties of AB_hRXG.•AB_hRXG shows the structural and functional characteristics of PMG-like group of IDPs.•AB_hRXG exhibits an ability to promote the formation of LLPS. The retinoid X receptor (RXR) is a member of the nuclear receptor (NR) superfamily...
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Veröffentlicht in: | The Journal of steroid biochemistry and molecular biology 2020-04, Vol.198, p.105571-105571, Article 105571 |
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container_title | The Journal of steroid biochemistry and molecular biology |
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creator | Sołtys, Katarzyna Ożyhar, Andrzej |
description | •We describe the biochemical and biophysical properties of AB_hRXG.•AB_hRXG shows the structural and functional characteristics of PMG-like group of IDPs.•AB_hRXG exhibits an ability to promote the formation of LLPS.
The retinoid X receptor (RXR) is a member of the nuclear receptor (NR) superfamily that occupies the central position among other NRs by forming both homodimers and heterodimers with other representatives of the family. RXR shares similar structural domains with other members of NRs. The major differences in the subtypes and isoforms of RXR are in the AB region. To date, there have been no data concerning the molecular properties of the AB region of hRXRγ (AB_hRXG). Here, we describe the biochemical and biophysical properties of the recombinant AB_hRXG. The results indicate that AB_hRXG shows the structural and functional characteristics of the pre-molten globule-like (PMG-like) group of intrinsically disordered proteins (IDPs) and also has a significant propensity for folding. We also present the first experimental evidence showing that the AB region of NRs promotes the formation of liquid–liquid phase separation (LLPS). |
doi_str_mv | 10.1016/j.jsbmb.2019.105571 |
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The retinoid X receptor (RXR) is a member of the nuclear receptor (NR) superfamily that occupies the central position among other NRs by forming both homodimers and heterodimers with other representatives of the family. RXR shares similar structural domains with other members of NRs. The major differences in the subtypes and isoforms of RXR are in the AB region. To date, there have been no data concerning the molecular properties of the AB region of hRXRγ (AB_hRXG). Here, we describe the biochemical and biophysical properties of the recombinant AB_hRXG. The results indicate that AB_hRXG shows the structural and functional characteristics of the pre-molten globule-like (PMG-like) group of intrinsically disordered proteins (IDPs) and also has a significant propensity for folding. We also present the first experimental evidence showing that the AB region of NRs promotes the formation of liquid–liquid phase separation (LLPS).</description><identifier>ISSN: 0960-0760</identifier><identifier>EISSN: 1879-1220</identifier><identifier>DOI: 10.1016/j.jsbmb.2019.105571</identifier><identifier>PMID: 31881311</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>AB region ; Intrinsically disordered protein/region ; Isoforms ; Liquid-liquid phase separation ; Nuclear receptor ; Retinoid X receptors ; RXR ; Structure-function relationships</subject><ispartof>The Journal of steroid biochemistry and molecular biology, 2020-04, Vol.198, p.105571-105571, Article 105571</ispartof><rights>2019 The Authors</rights><rights>Copyright © 2019 The Authors. Published by Elsevier Ltd.. All rights reserved.</rights><rights>Copyright Elsevier BV Apr 2020</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c432t-c3598d4d94977a1d1b5cab7a258cf401eed0e3cb29ce8f0ad5ca7bfa4a76873f3</citedby><cites>FETCH-LOGICAL-c432t-c3598d4d94977a1d1b5cab7a258cf401eed0e3cb29ce8f0ad5ca7bfa4a76873f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jsbmb.2019.105571$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31881311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sołtys, Katarzyna</creatorcontrib><creatorcontrib>Ożyhar, Andrzej</creatorcontrib><title>Ordered structure-forming properties of the intrinsically disordered AB region of hRXRγ and its ability to promote liquid-liquid phase separation</title><title>The Journal of steroid biochemistry and molecular biology</title><addtitle>J Steroid Biochem Mol Biol</addtitle><description>•We describe the biochemical and biophysical properties of AB_hRXG.•AB_hRXG shows the structural and functional characteristics of PMG-like group of IDPs.•AB_hRXG exhibits an ability to promote the formation of LLPS.
The retinoid X receptor (RXR) is a member of the nuclear receptor (NR) superfamily that occupies the central position among other NRs by forming both homodimers and heterodimers with other representatives of the family. RXR shares similar structural domains with other members of NRs. The major differences in the subtypes and isoforms of RXR are in the AB region. To date, there have been no data concerning the molecular properties of the AB region of hRXRγ (AB_hRXG). Here, we describe the biochemical and biophysical properties of the recombinant AB_hRXG. The results indicate that AB_hRXG shows the structural and functional characteristics of the pre-molten globule-like (PMG-like) group of intrinsically disordered proteins (IDPs) and also has a significant propensity for folding. We also present the first experimental evidence showing that the AB region of NRs promotes the formation of liquid–liquid phase separation (LLPS).</description><subject>AB region</subject><subject>Intrinsically disordered protein/region</subject><subject>Isoforms</subject><subject>Liquid-liquid phase separation</subject><subject>Nuclear receptor</subject><subject>Retinoid X receptors</subject><subject>RXR</subject><subject>Structure-function relationships</subject><issn>0960-0760</issn><issn>1879-1220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kc1q3DAUhUVpaKZpn6BQBN1k44l-bMtadJGG9AcCgdBCd0KWrjMytuVIcmFeI6-S9-gzVVNPu-iiqwtX3zm6nIPQG0q2lND6ot_2sR3bLSNU5k1VCfoMbWgjZEEZI8_RhsiaFETU5BS9jLEnhHBOxQt0ymnTUE7pBj3eBgsBLI4pLCYtAYrOh9FN93gOfoaQHETsO5x2gN2UgpuiM3oY9ti66I_iyw84wL3z04Hc3X2_-_mE9WSxSxHr1g0u7XHyB8fRJ8CDe1icLdaB552OgCPMOuiUPV6hk04PEV4f5xn69vH669Xn4ub205ery5vClJylwvBKNra0spRCaGppWxndCs2qxnQloQCWADctkwaajmibn0Xb6VKLuhG842fofPXNZz0sEJMaXTQwDHoCv0TFclgspyqqjL77B-39EqZ8nWIlr0tOpZCZ4itlgo8xQKfm4EYd9ooSdahM9ep3ZepQmVory6q3R--lHcH-1fzpKAPvVwByGD8cBBWNg8mAdQFMUta7_37wC4PkrGg</recordid><startdate>202004</startdate><enddate>202004</enddate><creator>Sołtys, Katarzyna</creator><creator>Ożyhar, Andrzej</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>202004</creationdate><title>Ordered structure-forming properties of the intrinsically disordered AB region of hRXRγ and its ability to promote liquid-liquid phase separation</title><author>Sołtys, Katarzyna ; Ożyhar, Andrzej</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c432t-c3598d4d94977a1d1b5cab7a258cf401eed0e3cb29ce8f0ad5ca7bfa4a76873f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>AB region</topic><topic>Intrinsically disordered protein/region</topic><topic>Isoforms</topic><topic>Liquid-liquid phase separation</topic><topic>Nuclear receptor</topic><topic>Retinoid X receptors</topic><topic>RXR</topic><topic>Structure-function relationships</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sołtys, Katarzyna</creatorcontrib><creatorcontrib>Ożyhar, Andrzej</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sołtys, Katarzyna</au><au>Ożyhar, Andrzej</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Ordered structure-forming properties of the intrinsically disordered AB region of hRXRγ and its ability to promote liquid-liquid phase separation</atitle><jtitle>The Journal of steroid biochemistry and molecular biology</jtitle><addtitle>J Steroid Biochem Mol Biol</addtitle><date>2020-04</date><risdate>2020</risdate><volume>198</volume><spage>105571</spage><epage>105571</epage><pages>105571-105571</pages><artnum>105571</artnum><issn>0960-0760</issn><eissn>1879-1220</eissn><abstract>•We describe the biochemical and biophysical properties of AB_hRXG.•AB_hRXG shows the structural and functional characteristics of PMG-like group of IDPs.•AB_hRXG exhibits an ability to promote the formation of LLPS.
The retinoid X receptor (RXR) is a member of the nuclear receptor (NR) superfamily that occupies the central position among other NRs by forming both homodimers and heterodimers with other representatives of the family. RXR shares similar structural domains with other members of NRs. The major differences in the subtypes and isoforms of RXR are in the AB region. To date, there have been no data concerning the molecular properties of the AB region of hRXRγ (AB_hRXG). Here, we describe the biochemical and biophysical properties of the recombinant AB_hRXG. The results indicate that AB_hRXG shows the structural and functional characteristics of the pre-molten globule-like (PMG-like) group of intrinsically disordered proteins (IDPs) and also has a significant propensity for folding. We also present the first experimental evidence showing that the AB region of NRs promotes the formation of liquid–liquid phase separation (LLPS).</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31881311</pmid><doi>10.1016/j.jsbmb.2019.105571</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | AB region Intrinsically disordered protein/region Isoforms Liquid-liquid phase separation Nuclear receptor Retinoid X receptors RXR Structure-function relationships |
title | Ordered structure-forming properties of the intrinsically disordered AB region of hRXRγ and its ability to promote liquid-liquid phase separation |
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