Loading…
MT1 melatonin receptor mRNA expression exhibits a circadian variation in the rat suprachiasmatic nuclei
The aim of the present study was to investigate the daily regulation of both MT1 and MT2 melatonin receptor subtype mRNA expression in the rat SCN in order to clarify their role in the daily variation of SCN melatonin receptors. Existing MT1 and MT2 partial clones were extended by PCR to 982 and 522...
Saved in:
Published in: | Brain research 2002-08, Vol.946 (1), p.64-71 |
---|---|
Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3 |
---|---|
cites | cdi_FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3 |
container_end_page | 71 |
container_issue | 1 |
container_start_page | 64 |
container_title | Brain research |
container_volume | 946 |
creator | Poirel, Vincent-Joseph Masson-Pévet, Mireille Pevét, Paul Gauer, François |
description | The aim of the present study was to investigate the daily regulation of both MT1 and MT2 melatonin receptor subtype mRNA expression in the rat SCN in order to clarify their role in the daily variation of SCN melatonin receptors. Existing MT1 and MT2 partial clones were extended by PCR to 982 and 522 bp, respectively. However, while the MT1 clone allowed us to set up a highly sensitive in situ hybridization (ISH) method, we could not detect MT2 expression within the SCN. Therefore, our results suggest that only MT1 mRNA can be correlated with 2-iodo-melatonin binding sites in the rat SCN. Investigation of MT1 mRNA expression throughout the 24 h light/dark cycle or in constant darkness clearly showed that in the two conditions, mRNA expression showed a robust rhythm with two peaks, one after the day/night and one after the night/day transitions in LD, and at the beginning of the subjective night and day in DD, respectively. Furthermore, these variations were not linked to the daily changes in melatonin receptor density. Thus, the transcriptional regulation of MT1 receptors does not appear to play a role in the daily regulation of melatonin binding sites availability. |
doi_str_mv | 10.1016/S0006-8993(02)02824-X |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71922059</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S000689930202824X</els_id><sourcerecordid>71922059</sourcerecordid><originalsourceid>FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3</originalsourceid><addsrcrecordid>eNqFkVtrFTEUhYNY7LH6E5S8WPRhNLeZZJ6klHqBqqAV-hb2JHs8kbmZZEr99-b0HOxjn3Y261tJWIuQF5y95Yw3734wxprKtK18zcQbJoxQ1fUjsuFGi6oRij0mm__IMXma0u-yStmyJ-SYCy5l3dYb8uvLFacjDpDnKUw0osMlz5GO37-eUbxdIqYU5qkct6ELOVGgLkQHPsBEbyAGyDu5WPMWaYRM07pEcNsAaSyao9PqBgzPyFEPQ8Lnh3lCfn64uDr_VF1--_j5_OyyckqIXEkJrVK1Et4I7E3Xt5p71Zvaa9050EpDKx3zotGm4wy7xtcNNB5877mue3lCTvf3LnH-s2LKdgzJ4TDAhPOarOatEKxuHwS5UbVgShew3oMuzilF7O0Swwjxr-XM7qqwd1XYXc6WCXtXhb0uvpeHB9ZuRH_vOmRfgFcHAJKDoY8wuZDuOWmUVMwU7v2ew5LbTcBokws4OfSh1JWtn8MDX_kHEsum1g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>18452047</pqid></control><display><type>article</type><title>MT1 melatonin receptor mRNA expression exhibits a circadian variation in the rat suprachiasmatic nuclei</title><source>Elsevier</source><creator>Poirel, Vincent-Joseph ; Masson-Pévet, Mireille ; Pevét, Paul ; Gauer, François</creator><creatorcontrib>Poirel, Vincent-Joseph ; Masson-Pévet, Mireille ; Pevét, Paul ; Gauer, François</creatorcontrib><description>The aim of the present study was to investigate the daily regulation of both MT1 and MT2 melatonin receptor subtype mRNA expression in the rat SCN in order to clarify their role in the daily variation of SCN melatonin receptors. Existing MT1 and MT2 partial clones were extended by PCR to 982 and 522 bp, respectively. However, while the MT1 clone allowed us to set up a highly sensitive in situ hybridization (ISH) method, we could not detect MT2 expression within the SCN. Therefore, our results suggest that only MT1 mRNA can be correlated with 2-iodo-melatonin binding sites in the rat SCN. Investigation of MT1 mRNA expression throughout the 24 h light/dark cycle or in constant darkness clearly showed that in the two conditions, mRNA expression showed a robust rhythm with two peaks, one after the day/night and one after the night/day transitions in LD, and at the beginning of the subjective night and day in DD, respectively. Furthermore, these variations were not linked to the daily changes in melatonin receptor density. Thus, the transcriptional regulation of MT1 receptors does not appear to play a role in the daily regulation of melatonin binding sites availability.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/S0006-8993(02)02824-X</identifier><identifier>PMID: 12133595</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Amino Acid Sequence - genetics ; Animals ; Base Sequence - genetics ; Biological and medical sciences ; Circadian clock ; Circadian Rhythm ; Fundamental and applied biological sciences. Psychology ; Hormones and neuropeptides. Regulation ; Hypothalamus. Hypophysis. Epiphysis. Urophysis ; Male ; Melatonin ; Melatonin receptor ; Molecular Sequence Data ; MT1 mRNA ; Rats ; Rats, Wistar ; Receptors, Cell Surface - genetics ; Receptors, Cytoplasmic and Nuclear - genetics ; Receptors, Melatonin ; RNA, Messenger - metabolism ; Suprachiasmatic nucleus ; Suprachiasmatic Nucleus - metabolism ; Vertebrates: endocrinology</subject><ispartof>Brain research, 2002-08, Vol.946 (1), p.64-71</ispartof><rights>2002 Elsevier Science B.V.</rights><rights>2002 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3</citedby><cites>FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13843408$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12133595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Poirel, Vincent-Joseph</creatorcontrib><creatorcontrib>Masson-Pévet, Mireille</creatorcontrib><creatorcontrib>Pevét, Paul</creatorcontrib><creatorcontrib>Gauer, François</creatorcontrib><title>MT1 melatonin receptor mRNA expression exhibits a circadian variation in the rat suprachiasmatic nuclei</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>The aim of the present study was to investigate the daily regulation of both MT1 and MT2 melatonin receptor subtype mRNA expression in the rat SCN in order to clarify their role in the daily variation of SCN melatonin receptors. Existing MT1 and MT2 partial clones were extended by PCR to 982 and 522 bp, respectively. However, while the MT1 clone allowed us to set up a highly sensitive in situ hybridization (ISH) method, we could not detect MT2 expression within the SCN. Therefore, our results suggest that only MT1 mRNA can be correlated with 2-iodo-melatonin binding sites in the rat SCN. Investigation of MT1 mRNA expression throughout the 24 h light/dark cycle or in constant darkness clearly showed that in the two conditions, mRNA expression showed a robust rhythm with two peaks, one after the day/night and one after the night/day transitions in LD, and at the beginning of the subjective night and day in DD, respectively. Furthermore, these variations were not linked to the daily changes in melatonin receptor density. Thus, the transcriptional regulation of MT1 receptors does not appear to play a role in the daily regulation of melatonin binding sites availability.</description><subject>Amino Acid Sequence - genetics</subject><subject>Animals</subject><subject>Base Sequence - genetics</subject><subject>Biological and medical sciences</subject><subject>Circadian clock</subject><subject>Circadian Rhythm</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hormones and neuropeptides. Regulation</subject><subject>Hypothalamus. Hypophysis. Epiphysis. Urophysis</subject><subject>Male</subject><subject>Melatonin</subject><subject>Melatonin receptor</subject><subject>Molecular Sequence Data</subject><subject>MT1 mRNA</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Receptors, Cell Surface - genetics</subject><subject>Receptors, Cytoplasmic and Nuclear - genetics</subject><subject>Receptors, Melatonin</subject><subject>RNA, Messenger - metabolism</subject><subject>Suprachiasmatic nucleus</subject><subject>Suprachiasmatic Nucleus - metabolism</subject><subject>Vertebrates: endocrinology</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNqFkVtrFTEUhYNY7LH6E5S8WPRhNLeZZJ6klHqBqqAV-hb2JHs8kbmZZEr99-b0HOxjn3Y261tJWIuQF5y95Yw3734wxprKtK18zcQbJoxQ1fUjsuFGi6oRij0mm__IMXma0u-yStmyJ-SYCy5l3dYb8uvLFacjDpDnKUw0osMlz5GO37-eUbxdIqYU5qkct6ELOVGgLkQHPsBEbyAGyDu5WPMWaYRM07pEcNsAaSyao9PqBgzPyFEPQ8Lnh3lCfn64uDr_VF1--_j5_OyyckqIXEkJrVK1Et4I7E3Xt5p71Zvaa9050EpDKx3zotGm4wy7xtcNNB5877mue3lCTvf3LnH-s2LKdgzJ4TDAhPOarOatEKxuHwS5UbVgShew3oMuzilF7O0Swwjxr-XM7qqwd1XYXc6WCXtXhb0uvpeHB9ZuRH_vOmRfgFcHAJKDoY8wuZDuOWmUVMwU7v2ew5LbTcBokws4OfSh1JWtn8MDX_kHEsum1g</recordid><startdate>20020809</startdate><enddate>20020809</enddate><creator>Poirel, Vincent-Joseph</creator><creator>Masson-Pévet, Mireille</creator><creator>Pevét, Paul</creator><creator>Gauer, François</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</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>7TK</scope><scope>7X8</scope></search><sort><creationdate>20020809</creationdate><title>MT1 melatonin receptor mRNA expression exhibits a circadian variation in the rat suprachiasmatic nuclei</title><author>Poirel, Vincent-Joseph ; Masson-Pévet, Mireille ; Pevét, Paul ; Gauer, François</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Amino Acid Sequence - genetics</topic><topic>Animals</topic><topic>Base Sequence - genetics</topic><topic>Biological and medical sciences</topic><topic>Circadian clock</topic><topic>Circadian Rhythm</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hormones and neuropeptides. Regulation</topic><topic>Hypothalamus. Hypophysis. Epiphysis. Urophysis</topic><topic>Male</topic><topic>Melatonin</topic><topic>Melatonin receptor</topic><topic>Molecular Sequence Data</topic><topic>MT1 mRNA</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Receptors, Cell Surface - genetics</topic><topic>Receptors, Cytoplasmic and Nuclear - genetics</topic><topic>Receptors, Melatonin</topic><topic>RNA, Messenger - metabolism</topic><topic>Suprachiasmatic nucleus</topic><topic>Suprachiasmatic Nucleus - metabolism</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Poirel, Vincent-Joseph</creatorcontrib><creatorcontrib>Masson-Pévet, Mireille</creatorcontrib><creatorcontrib>Pevét, Paul</creatorcontrib><creatorcontrib>Gauer, François</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Poirel, Vincent-Joseph</au><au>Masson-Pévet, Mireille</au><au>Pevét, Paul</au><au>Gauer, François</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>MT1 melatonin receptor mRNA expression exhibits a circadian variation in the rat suprachiasmatic nuclei</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>2002-08-09</date><risdate>2002</risdate><volume>946</volume><issue>1</issue><spage>64</spage><epage>71</epage><pages>64-71</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>The aim of the present study was to investigate the daily regulation of both MT1 and MT2 melatonin receptor subtype mRNA expression in the rat SCN in order to clarify their role in the daily variation of SCN melatonin receptors. Existing MT1 and MT2 partial clones were extended by PCR to 982 and 522 bp, respectively. However, while the MT1 clone allowed us to set up a highly sensitive in situ hybridization (ISH) method, we could not detect MT2 expression within the SCN. Therefore, our results suggest that only MT1 mRNA can be correlated with 2-iodo-melatonin binding sites in the rat SCN. Investigation of MT1 mRNA expression throughout the 24 h light/dark cycle or in constant darkness clearly showed that in the two conditions, mRNA expression showed a robust rhythm with two peaks, one after the day/night and one after the night/day transitions in LD, and at the beginning of the subjective night and day in DD, respectively. Furthermore, these variations were not linked to the daily changes in melatonin receptor density. Thus, the transcriptional regulation of MT1 receptors does not appear to play a role in the daily regulation of melatonin binding sites availability.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>12133595</pmid><doi>10.1016/S0006-8993(02)02824-X</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0006-8993 |
ispartof | Brain research, 2002-08, Vol.946 (1), p.64-71 |
issn | 0006-8993 1872-6240 |
language | eng |
recordid | cdi_proquest_miscellaneous_71922059 |
source | Elsevier |
subjects | Amino Acid Sequence - genetics Animals Base Sequence - genetics Biological and medical sciences Circadian clock Circadian Rhythm Fundamental and applied biological sciences. Psychology Hormones and neuropeptides. Regulation Hypothalamus. Hypophysis. Epiphysis. Urophysis Male Melatonin Melatonin receptor Molecular Sequence Data MT1 mRNA Rats Rats, Wistar Receptors, Cell Surface - genetics Receptors, Cytoplasmic and Nuclear - genetics Receptors, Melatonin RNA, Messenger - metabolism Suprachiasmatic nucleus Suprachiasmatic Nucleus - metabolism Vertebrates: endocrinology |
title | MT1 melatonin receptor mRNA expression exhibits a circadian variation in the rat suprachiasmatic nuclei |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T10%3A24%3A08IST&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=MT1%20melatonin%20receptor%20mRNA%20expression%20exhibits%20a%20circadian%20variation%20in%20the%20rat%20suprachiasmatic%20nuclei&rft.jtitle=Brain%20research&rft.au=Poirel,%20Vincent-Joseph&rft.date=2002-08-09&rft.volume=946&rft.issue=1&rft.spage=64&rft.epage=71&rft.pages=64-71&rft.issn=0006-8993&rft.eissn=1872-6240&rft.coden=BRREAP&rft_id=info:doi/10.1016/S0006-8993(02)02824-X&rft_dat=%3Cproquest_cross%3E71922059%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c422t-33a944542d82ef8bf971d4f85d77bca747a93c0d2678b10eb6d56a6dadfd175f3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=18452047&rft_id=info:pmid/12133595&rfr_iscdi=true |