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mCRY1 and mCRY2 Are Essential Components of the Negative Limb of the Circadian Clock Feedback Loop
We determined that two mouse cryptochrome genes, mCry1 and mCry2, act in the negative limb of the clock feedback loop. In cell lines, mPER proteins (alone or in combination) have modest effects on their cellular location and ability to inhibit CLOCK:BMAL1-mediated transcription. This suggested crypt...
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Published in: | Cell 1999-07, Vol.98 (2), p.193-205 |
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container_end_page | 205 |
container_issue | 2 |
container_start_page | 193 |
container_title | Cell |
container_volume | 98 |
creator | Kume, Kazuhiko Zylka, Mark J Sriram, Sathyanarayanan Shearman, Lauren P Weaver, David R Jin, Xiaowei Maywood, Elizabeth S Hastings, Michael H Reppert, Steven M |
description | We determined that two mouse cryptochrome genes,
mCry1 and
mCry2, act in the negative limb of the clock feedback loop. In cell lines, mPER proteins (alone or in combination) have modest effects on their cellular location and ability to inhibit CLOCK:BMAL1-mediated transcription. This suggested cryptochrome involvement in the negative limb of the feedback loop. Indeed,
mCry1 and
mCry2 RNA levels are reduced in the central and peripheral clocks of
Clock/Clock mutant mice. mCRY1 and mCRY2 are nuclear proteins that interact with each of the mPER proteins, translocate each mPER protein from cytoplasm to nucleus, and are rhythmically expressed in the suprachiasmatic circadian clock. Luciferase reporter gene assays show that mCRY1 or mCRY2 alone abrogates CLOCK:BMAL1–E box–mediated transcription. The mPER and mCRY proteins appear to inhibit the transcriptional complex differentially. |
doi_str_mv | 10.1016/S0092-8674(00)81014-4 |
format | article |
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mCry1 and
mCry2, act in the negative limb of the clock feedback loop. In cell lines, mPER proteins (alone or in combination) have modest effects on their cellular location and ability to inhibit CLOCK:BMAL1-mediated transcription. This suggested cryptochrome involvement in the negative limb of the feedback loop. Indeed,
mCry1 and
mCry2 RNA levels are reduced in the central and peripheral clocks of
Clock/Clock mutant mice. mCRY1 and mCRY2 are nuclear proteins that interact with each of the mPER proteins, translocate each mPER protein from cytoplasm to nucleus, and are rhythmically expressed in the suprachiasmatic circadian clock. Luciferase reporter gene assays show that mCRY1 or mCRY2 alone abrogates CLOCK:BMAL1–E box–mediated transcription. The mPER and mCRY proteins appear to inhibit the transcriptional complex differentially.</description><identifier>ISSN: 0092-8674</identifier><identifier>EISSN: 1097-4172</identifier><identifier>DOI: 10.1016/S0092-8674(00)81014-4</identifier><identifier>PMID: 10428031</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3T3 Cells ; Animals ; ARNTL Transcription Factors ; Basic Helix-Loop-Helix Transcription Factors ; Biological Clocks - physiology ; Blotting, Western ; Cell Cycle Proteins ; Cell Nucleus - metabolism ; CLOCK Proteins ; Cloning, Molecular ; COS Cells ; Cryptochromes ; Drosophila Proteins ; Eye Proteins ; Feedback - physiology ; Female ; Flavoproteins - analysis ; Flavoproteins - genetics ; Flavoproteins - metabolism ; Gene Expression - physiology ; Humans ; Male ; Mice ; Mice, Inbred BALB C ; Mice, Knockout ; Molecular Sequence Data ; Nuclear Proteins - genetics ; Nuclear Proteins - metabolism ; Period Circadian Proteins ; Photoreceptor Cells, Invertebrate ; Receptors, G-Protein-Coupled ; RNA, Messenger - metabolism ; Suprachiasmatic Nucleus - chemistry ; Suprachiasmatic Nucleus - metabolism ; Trans-Activators - genetics ; Trans-Activators - metabolism ; Transcription Factors - genetics ; Transcription Factors - metabolism ; Transcription, Genetic - physiology</subject><ispartof>Cell, 1999-07, Vol.98 (2), p.193-205</ispartof><rights>1999 Cell Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c557t-fcf8cc7b6f9063539ae0b2553ab937afa842e1ba5854b308db9e427410abe8a3</citedby><cites>FETCH-LOGICAL-c557t-fcf8cc7b6f9063539ae0b2553ab937afa842e1ba5854b308db9e427410abe8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0092867400810144$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3549,27924,27925,45780</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10428031$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kume, Kazuhiko</creatorcontrib><creatorcontrib>Zylka, Mark J</creatorcontrib><creatorcontrib>Sriram, Sathyanarayanan</creatorcontrib><creatorcontrib>Shearman, Lauren P</creatorcontrib><creatorcontrib>Weaver, David R</creatorcontrib><creatorcontrib>Jin, Xiaowei</creatorcontrib><creatorcontrib>Maywood, Elizabeth S</creatorcontrib><creatorcontrib>Hastings, Michael H</creatorcontrib><creatorcontrib>Reppert, Steven M</creatorcontrib><title>mCRY1 and mCRY2 Are Essential Components of the Negative Limb of the Circadian Clock Feedback Loop</title><title>Cell</title><addtitle>Cell</addtitle><description>We determined that two mouse cryptochrome genes,
mCry1 and
mCry2, act in the negative limb of the clock feedback loop. In cell lines, mPER proteins (alone or in combination) have modest effects on their cellular location and ability to inhibit CLOCK:BMAL1-mediated transcription. This suggested cryptochrome involvement in the negative limb of the feedback loop. Indeed,
mCry1 and
mCry2 RNA levels are reduced in the central and peripheral clocks of
Clock/Clock mutant mice. mCRY1 and mCRY2 are nuclear proteins that interact with each of the mPER proteins, translocate each mPER protein from cytoplasm to nucleus, and are rhythmically expressed in the suprachiasmatic circadian clock. Luciferase reporter gene assays show that mCRY1 or mCRY2 alone abrogates CLOCK:BMAL1–E box–mediated transcription. The mPER and mCRY proteins appear to inhibit the transcriptional complex differentially.</description><subject>3T3 Cells</subject><subject>Animals</subject><subject>ARNTL Transcription Factors</subject><subject>Basic Helix-Loop-Helix Transcription Factors</subject><subject>Biological Clocks - physiology</subject><subject>Blotting, Western</subject><subject>Cell Cycle Proteins</subject><subject>Cell Nucleus - metabolism</subject><subject>CLOCK Proteins</subject><subject>Cloning, Molecular</subject><subject>COS Cells</subject><subject>Cryptochromes</subject><subject>Drosophila Proteins</subject><subject>Eye Proteins</subject><subject>Feedback - physiology</subject><subject>Female</subject><subject>Flavoproteins - analysis</subject><subject>Flavoproteins - genetics</subject><subject>Flavoproteins - metabolism</subject><subject>Gene Expression - physiology</subject><subject>Humans</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Mice, Knockout</subject><subject>Molecular Sequence Data</subject><subject>Nuclear Proteins - genetics</subject><subject>Nuclear Proteins - metabolism</subject><subject>Period Circadian Proteins</subject><subject>Photoreceptor Cells, Invertebrate</subject><subject>Receptors, G-Protein-Coupled</subject><subject>RNA, Messenger - metabolism</subject><subject>Suprachiasmatic Nucleus - chemistry</subject><subject>Suprachiasmatic Nucleus - metabolism</subject><subject>Trans-Activators - genetics</subject><subject>Trans-Activators - metabolism</subject><subject>Transcription Factors - genetics</subject><subject>Transcription Factors - metabolism</subject><subject>Transcription, Genetic - physiology</subject><issn>0092-8674</issn><issn>1097-4172</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkUtP3DAUhS1UxAyPn0DlVQWL0OvYTpxVhSJoK41AKmxYWbZzQw1JPLUzI_XfN_MAdcfqPvTde6RzCDlncMWAFV8fAKo8U0UpLgAu1bQTmTggcwZVmQlW5p_I_B2ZkeOUXgBASSmPyIyByBVwNie2r389MWqGhm66nF5HpDcp4TB609E69MswTEOioaXjb6R3-GxGv0a68L19W9Y-OtN4M9C6C-6V3iI21kzNIoTlKTlsTZfwbF9PyOPtzWP9I1vcf_9ZXy8yJ2U5Zq1rlXOlLdoKCi55ZRBsLiU3tuKlaY0SOTJrpJLCclCNrVDkpWBgLCrDT8iX3dtlDH9WmEbd--Sw68yAYZV0UVWc80J8CLKSM65UPoFyB7oYUorY6mX0vYl_NQO9CUFvQ9AbhzWA3oagNwKf9wIr22Pz39XO9Qn4tgNwsmPtMerkPA4OGx_RjboJ_gOJf3WalNg</recordid><startdate>19990723</startdate><enddate>19990723</enddate><creator>Kume, Kazuhiko</creator><creator>Zylka, Mark J</creator><creator>Sriram, Sathyanarayanan</creator><creator>Shearman, Lauren P</creator><creator>Weaver, David R</creator><creator>Jin, Xiaowei</creator><creator>Maywood, Elizabeth S</creator><creator>Hastings, Michael H</creator><creator>Reppert, Steven M</creator><general>Elsevier Inc</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19990723</creationdate><title>mCRY1 and mCRY2 Are Essential Components of the Negative Limb of the Circadian Clock Feedback Loop</title><author>Kume, Kazuhiko ; Zylka, Mark J ; Sriram, Sathyanarayanan ; Shearman, Lauren P ; Weaver, David R ; Jin, Xiaowei ; Maywood, Elizabeth S ; Hastings, Michael H ; Reppert, Steven M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c557t-fcf8cc7b6f9063539ae0b2553ab937afa842e1ba5854b308db9e427410abe8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>3T3 Cells</topic><topic>Animals</topic><topic>ARNTL Transcription Factors</topic><topic>Basic Helix-Loop-Helix Transcription Factors</topic><topic>Biological Clocks - physiology</topic><topic>Blotting, Western</topic><topic>Cell Cycle Proteins</topic><topic>Cell Nucleus - metabolism</topic><topic>CLOCK Proteins</topic><topic>Cloning, Molecular</topic><topic>COS Cells</topic><topic>Cryptochromes</topic><topic>Drosophila Proteins</topic><topic>Eye Proteins</topic><topic>Feedback - physiology</topic><topic>Female</topic><topic>Flavoproteins - analysis</topic><topic>Flavoproteins - genetics</topic><topic>Flavoproteins - metabolism</topic><topic>Gene Expression - physiology</topic><topic>Humans</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Mice, Knockout</topic><topic>Molecular Sequence Data</topic><topic>Nuclear Proteins - genetics</topic><topic>Nuclear Proteins - metabolism</topic><topic>Period Circadian Proteins</topic><topic>Photoreceptor Cells, Invertebrate</topic><topic>Receptors, G-Protein-Coupled</topic><topic>RNA, Messenger - metabolism</topic><topic>Suprachiasmatic Nucleus - chemistry</topic><topic>Suprachiasmatic Nucleus - metabolism</topic><topic>Trans-Activators - genetics</topic><topic>Trans-Activators - metabolism</topic><topic>Transcription Factors - genetics</topic><topic>Transcription Factors - metabolism</topic><topic>Transcription, Genetic - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kume, Kazuhiko</creatorcontrib><creatorcontrib>Zylka, Mark J</creatorcontrib><creatorcontrib>Sriram, Sathyanarayanan</creatorcontrib><creatorcontrib>Shearman, Lauren P</creatorcontrib><creatorcontrib>Weaver, David R</creatorcontrib><creatorcontrib>Jin, Xiaowei</creatorcontrib><creatorcontrib>Maywood, Elizabeth S</creatorcontrib><creatorcontrib>Hastings, Michael H</creatorcontrib><creatorcontrib>Reppert, Steven M</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Cell</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kume, Kazuhiko</au><au>Zylka, Mark J</au><au>Sriram, Sathyanarayanan</au><au>Shearman, Lauren P</au><au>Weaver, David R</au><au>Jin, Xiaowei</au><au>Maywood, Elizabeth S</au><au>Hastings, Michael H</au><au>Reppert, Steven M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>mCRY1 and mCRY2 Are Essential Components of the Negative Limb of the Circadian Clock Feedback Loop</atitle><jtitle>Cell</jtitle><addtitle>Cell</addtitle><date>1999-07-23</date><risdate>1999</risdate><volume>98</volume><issue>2</issue><spage>193</spage><epage>205</epage><pages>193-205</pages><issn>0092-8674</issn><eissn>1097-4172</eissn><abstract>We determined that two mouse cryptochrome genes,
mCry1 and
mCry2, act in the negative limb of the clock feedback loop. In cell lines, mPER proteins (alone or in combination) have modest effects on their cellular location and ability to inhibit CLOCK:BMAL1-mediated transcription. This suggested cryptochrome involvement in the negative limb of the feedback loop. Indeed,
mCry1 and
mCry2 RNA levels are reduced in the central and peripheral clocks of
Clock/Clock mutant mice. mCRY1 and mCRY2 are nuclear proteins that interact with each of the mPER proteins, translocate each mPER protein from cytoplasm to nucleus, and are rhythmically expressed in the suprachiasmatic circadian clock. Luciferase reporter gene assays show that mCRY1 or mCRY2 alone abrogates CLOCK:BMAL1–E box–mediated transcription. The mPER and mCRY proteins appear to inhibit the transcriptional complex differentially.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>10428031</pmid><doi>10.1016/S0092-8674(00)81014-4</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3T3 Cells Animals ARNTL Transcription Factors Basic Helix-Loop-Helix Transcription Factors Biological Clocks - physiology Blotting, Western Cell Cycle Proteins Cell Nucleus - metabolism CLOCK Proteins Cloning, Molecular COS Cells Cryptochromes Drosophila Proteins Eye Proteins Feedback - physiology Female Flavoproteins - analysis Flavoproteins - genetics Flavoproteins - metabolism Gene Expression - physiology Humans Male Mice Mice, Inbred BALB C Mice, Knockout Molecular Sequence Data Nuclear Proteins - genetics Nuclear Proteins - metabolism Period Circadian Proteins Photoreceptor Cells, Invertebrate Receptors, G-Protein-Coupled RNA, Messenger - metabolism Suprachiasmatic Nucleus - chemistry Suprachiasmatic Nucleus - metabolism Trans-Activators - genetics Trans-Activators - metabolism Transcription Factors - genetics Transcription Factors - metabolism Transcription, Genetic - physiology |
title | mCRY1 and mCRY2 Are Essential Components of the Negative Limb of the Circadian Clock Feedback Loop |
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