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Dityrosine bridge formation and thyroid hormone synthesis are tightly linked and are both dependent on N-glycans
Formation of dityrosine bridges is a ubiquitous process mainly attributed to oxidative stress leading to protein degradation and cellular damages. Here we show that dityrosine formation is involved in a physiological process, thyroid hormone synthesis, and is strictly dependent on structural charact...
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Published in: | FEBS letters 1996-11, Vol.396 (2), p.223-226 |
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creator | Baudry, Nathalie Lejeune, Pierre-Jean Niccoli, Patricia Vinet, Liliane Carayon, Pierre Mallet, Bernard |
description | Formation of dityrosine bridges is a ubiquitous process mainly attributed to oxidative stress leading to protein degradation and cellular damages. Here we show that dityrosine formation is involved in a physiological process, thyroid hormone synthesis, and is strictly dependent on structural characteristics, namely
N-glycans, presented by the protein acting as the prothyroid hormone. We used two isoforms of the N-terminal thyroid hormone forming domain (NTD) of human thyroglobulin: one without
N-glycan (19 kDa isoform) and the other with high mannose type structures (25 kDa isoform). Both isoforms were able to form iodotyrosines after in vitro iodination. However, iodotyrosine coupling to form thyroxine did not occur with the unglycosylated 19 kDa NTD. In contrast, the 25 kDa isoform formed thyroxine. Strikingly, thyroxine synthesis was accompanied by dimerization of the 25 kDa isoform and formation of a dityrosine bridge; none of this was observed with the 19 kDa isoform. Taken as a whole, our results indicate that dimerization through dityrosine bridging accompanies and could have a role in thyroid hormone synthesis. |
doi_str_mv | 10.1016/0014-5793(96)01107-6 |
format | article |
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N-glycans, presented by the protein acting as the prothyroid hormone. We used two isoforms of the N-terminal thyroid hormone forming domain (NTD) of human thyroglobulin: one without
N-glycan (19 kDa isoform) and the other with high mannose type structures (25 kDa isoform). Both isoforms were able to form iodotyrosines after in vitro iodination. However, iodotyrosine coupling to form thyroxine did not occur with the unglycosylated 19 kDa NTD. In contrast, the 25 kDa isoform formed thyroxine. Strikingly, thyroxine synthesis was accompanied by dimerization of the 25 kDa isoform and formation of a dityrosine bridge; none of this was observed with the 19 kDa isoform. Taken as a whole, our results indicate that dimerization through dityrosine bridging accompanies and could have a role in thyroid hormone synthesis.</description><identifier>ISSN: 0014-5793</identifier><identifier>EISSN: 1873-3468</identifier><identifier>DOI: 10.1016/0014-5793(96)01107-6</identifier><identifier>PMID: 8914991</identifier><language>eng</language><publisher>England: Elsevier B.V</publisher><subject>ConA ; concanavalin A ; diiodotyrosine ; Dimerization ; DIT ; Dityrosine ; Glycosylation ; Hormone synthesis ; Humans ; lactoperoxidase ; LPO ; Mannose - chemistry ; MIT ; monoiodotyrosine ; Monoiodotyrosine - analysis ; Polysaccharides - chemistry ; RCA120 ; Ricinus communis agglutinin ; SDS-PAGE ; sodium dodecyl sulfate polyacrylamide gel electrophoresis ; thyroglobulin ; Thyroglobulin - chemistry ; Thyroglobulin - metabolism ; Thyroid ; thyroperoxidase ; thyroxine ; Thyroxine - biosynthesis ; TPO ; triiodothyronine ; Tyrosine - analogs & derivatives ; Tyrosine - chemistry</subject><ispartof>FEBS letters, 1996-11, Vol.396 (2), p.223-226</ispartof><rights>1996</rights><rights>FEBS Letters 396 (1996) 1873-3468 © 2015 Federation of European Biochemical Societies</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4666-108f66efbd98ae034b1277c5b14637ed34c64b59cd3e6c3afa2c370651a864ac3</citedby><cites>FETCH-LOGICAL-c4666-108f66efbd98ae034b1277c5b14637ed34c64b59cd3e6c3afa2c370651a864ac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0014579396011076$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8914991$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baudry, Nathalie</creatorcontrib><creatorcontrib>Lejeune, Pierre-Jean</creatorcontrib><creatorcontrib>Niccoli, Patricia</creatorcontrib><creatorcontrib>Vinet, Liliane</creatorcontrib><creatorcontrib>Carayon, Pierre</creatorcontrib><creatorcontrib>Mallet, Bernard</creatorcontrib><title>Dityrosine bridge formation and thyroid hormone synthesis are tightly linked and are both dependent on N-glycans</title><title>FEBS letters</title><addtitle>FEBS Lett</addtitle><description>Formation of dityrosine bridges is a ubiquitous process mainly attributed to oxidative stress leading to protein degradation and cellular damages. Here we show that dityrosine formation is involved in a physiological process, thyroid hormone synthesis, and is strictly dependent on structural characteristics, namely
N-glycans, presented by the protein acting as the prothyroid hormone. We used two isoforms of the N-terminal thyroid hormone forming domain (NTD) of human thyroglobulin: one without
N-glycan (19 kDa isoform) and the other with high mannose type structures (25 kDa isoform). Both isoforms were able to form iodotyrosines after in vitro iodination. However, iodotyrosine coupling to form thyroxine did not occur with the unglycosylated 19 kDa NTD. In contrast, the 25 kDa isoform formed thyroxine. Strikingly, thyroxine synthesis was accompanied by dimerization of the 25 kDa isoform and formation of a dityrosine bridge; none of this was observed with the 19 kDa isoform. Taken as a whole, our results indicate that dimerization through dityrosine bridging accompanies and could have a role in thyroid hormone synthesis.</description><subject>ConA</subject><subject>concanavalin A</subject><subject>diiodotyrosine</subject><subject>Dimerization</subject><subject>DIT</subject><subject>Dityrosine</subject><subject>Glycosylation</subject><subject>Hormone synthesis</subject><subject>Humans</subject><subject>lactoperoxidase</subject><subject>LPO</subject><subject>Mannose - chemistry</subject><subject>MIT</subject><subject>monoiodotyrosine</subject><subject>Monoiodotyrosine - analysis</subject><subject>Polysaccharides - chemistry</subject><subject>RCA120</subject><subject>Ricinus communis agglutinin</subject><subject>SDS-PAGE</subject><subject>sodium dodecyl sulfate polyacrylamide gel electrophoresis</subject><subject>thyroglobulin</subject><subject>Thyroglobulin - chemistry</subject><subject>Thyroglobulin - metabolism</subject><subject>Thyroid</subject><subject>thyroperoxidase</subject><subject>thyroxine</subject><subject>Thyroxine - biosynthesis</subject><subject>TPO</subject><subject>triiodothyronine</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - chemistry</subject><issn>0014-5793</issn><issn>1873-3468</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><recordid>eNqNkEFv3CAQhVHVKNmm_QeJxKlqD05gwWAuldI020aK0kt7RhjGaxIv3gDbyv8-OLvKseoJzXtv3qAPoTNKLiih4pIQyqtaKvZJic-EUiIr8QYtaCNZxbho3qLFa-QEvUvpgZS5oeoYHTeKcqXoAm2_-TzFMfkAuI3erQF3Y9yY7MeATXA498X2DvdFHUsoTSH3kHzCJgLOft3nYcKDD4_gXhZmuR1zjx1sITgIGZeq-2o9TNaE9B4ddWZI8OHwnqLfq5tf1z-qu5_fb6-v7irLhRAVJU0nBHStU40BwnhLl1LauqVcMAmOcSt4WyvrGAjLTGeWlkkiamoawY1lp-jjvncbx6cdpKw3PlkYBhNg3CUtm3rJmZAlyPdBWzCkCJ3eRr8xcdKU6Bm0ninqmaJWZZhBa1HWzg_9u3YD7nXpQLb4q73_1w8w_VenXt18Xc7GrCvxos6HvuyLoND64yHqZD0EC85HsFm70f_7p8_Jo6Ge</recordid><startdate>19961104</startdate><enddate>19961104</enddate><creator>Baudry, Nathalie</creator><creator>Lejeune, Pierre-Jean</creator><creator>Niccoli, Patricia</creator><creator>Vinet, Liliane</creator><creator>Carayon, Pierre</creator><creator>Mallet, Bernard</creator><general>Elsevier B.V</general><scope>6I.</scope><scope>AAFTH</scope><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>19961104</creationdate><title>Dityrosine bridge formation and thyroid hormone synthesis are tightly linked and are both dependent on N-glycans</title><author>Baudry, Nathalie ; Lejeune, Pierre-Jean ; Niccoli, Patricia ; Vinet, Liliane ; Carayon, Pierre ; Mallet, Bernard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4666-108f66efbd98ae034b1277c5b14637ed34c64b59cd3e6c3afa2c370651a864ac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>ConA</topic><topic>concanavalin A</topic><topic>diiodotyrosine</topic><topic>Dimerization</topic><topic>DIT</topic><topic>Dityrosine</topic><topic>Glycosylation</topic><topic>Hormone synthesis</topic><topic>Humans</topic><topic>lactoperoxidase</topic><topic>LPO</topic><topic>Mannose - chemistry</topic><topic>MIT</topic><topic>monoiodotyrosine</topic><topic>Monoiodotyrosine - analysis</topic><topic>Polysaccharides - chemistry</topic><topic>RCA120</topic><topic>Ricinus communis agglutinin</topic><topic>SDS-PAGE</topic><topic>sodium dodecyl sulfate polyacrylamide gel electrophoresis</topic><topic>thyroglobulin</topic><topic>Thyroglobulin - chemistry</topic><topic>Thyroglobulin - metabolism</topic><topic>Thyroid</topic><topic>thyroperoxidase</topic><topic>thyroxine</topic><topic>Thyroxine - biosynthesis</topic><topic>TPO</topic><topic>triiodothyronine</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Tyrosine - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baudry, Nathalie</creatorcontrib><creatorcontrib>Lejeune, Pierre-Jean</creatorcontrib><creatorcontrib>Niccoli, Patricia</creatorcontrib><creatorcontrib>Vinet, Liliane</creatorcontrib><creatorcontrib>Carayon, Pierre</creatorcontrib><creatorcontrib>Mallet, Bernard</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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>FEBS letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baudry, Nathalie</au><au>Lejeune, Pierre-Jean</au><au>Niccoli, Patricia</au><au>Vinet, Liliane</au><au>Carayon, Pierre</au><au>Mallet, Bernard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dityrosine bridge formation and thyroid hormone synthesis are tightly linked and are both dependent on N-glycans</atitle><jtitle>FEBS letters</jtitle><addtitle>FEBS Lett</addtitle><date>1996-11-04</date><risdate>1996</risdate><volume>396</volume><issue>2</issue><spage>223</spage><epage>226</epage><pages>223-226</pages><issn>0014-5793</issn><eissn>1873-3468</eissn><abstract>Formation of dityrosine bridges is a ubiquitous process mainly attributed to oxidative stress leading to protein degradation and cellular damages. Here we show that dityrosine formation is involved in a physiological process, thyroid hormone synthesis, and is strictly dependent on structural characteristics, namely
N-glycans, presented by the protein acting as the prothyroid hormone. We used two isoforms of the N-terminal thyroid hormone forming domain (NTD) of human thyroglobulin: one without
N-glycan (19 kDa isoform) and the other with high mannose type structures (25 kDa isoform). Both isoforms were able to form iodotyrosines after in vitro iodination. However, iodotyrosine coupling to form thyroxine did not occur with the unglycosylated 19 kDa NTD. In contrast, the 25 kDa isoform formed thyroxine. Strikingly, thyroxine synthesis was accompanied by dimerization of the 25 kDa isoform and formation of a dityrosine bridge; none of this was observed with the 19 kDa isoform. Taken as a whole, our results indicate that dimerization through dityrosine bridging accompanies and could have a role in thyroid hormone synthesis.</abstract><cop>England</cop><pub>Elsevier B.V</pub><pmid>8914991</pmid><doi>10.1016/0014-5793(96)01107-6</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | ConA concanavalin A diiodotyrosine Dimerization DIT Dityrosine Glycosylation Hormone synthesis Humans lactoperoxidase LPO Mannose - chemistry MIT monoiodotyrosine Monoiodotyrosine - analysis Polysaccharides - chemistry RCA120 Ricinus communis agglutinin SDS-PAGE sodium dodecyl sulfate polyacrylamide gel electrophoresis thyroglobulin Thyroglobulin - chemistry Thyroglobulin - metabolism Thyroid thyroperoxidase thyroxine Thyroxine - biosynthesis TPO triiodothyronine Tyrosine - analogs & derivatives Tyrosine - chemistry |
title | Dityrosine bridge formation and thyroid hormone synthesis are tightly linked and are both dependent on N-glycans |
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