Methylation status and chromatin structure of an early response gene (ornithine decarboxylase) in resting and stimulated NIH-3T3 fibroblasts
The early response gene ornithine decarboxylase (odc) is indispensable for normal and malignant cell growth. Although DNA methylation is generally associated with chromatin condensation and gene inactivation, the odc gene is heavily methylated at CCGG‐sequences in animal cell lines. In this work we...
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Veröffentlicht in: | Journal of cellular biochemistry 1994-06, Vol.55 (2), p.155-167 |
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description | The early response gene ornithine decarboxylase (odc) is indispensable for normal and malignant cell growth. Although DNA methylation is generally associated with chromatin condensation and gene inactivation, the odc gene is heavily methylated at CCGG‐sequences in animal cell lines. In this work we analyzed the chromatin structure and the DNA methylation status at the CpG‐rich promoter sequences at the odc locus in mouse 3T3 fibroblasts. We show that the proximal promoter region of the odc locus is not hypermethylated, while the distal promoter sequences appear to have a few methylated CCGG‐sites and display methylation polymorphism. Furthermore, it was found that the 5′ promoter region of odc is constitutively more sensitive to micrococcal nuclease than the coding and 3′ regions of the odc gene. Stimulation of the cells with serum resulted in an appearance of a DNase I sensitive site at the promoter region. The chromatin structure of the mid‐coding and 3′ regions of the odc gene also underwent structural changes that were accompanied by the rapid accumulation of odc mRNA. Such changes were not detected in the chromatin structure of glyceraldehyde‐3‐phosphate dehydrogenase (gadph) gene, whose expression remains invariant upon serum stimulation. These data suggest that the chromatin structure may play an important role in the rapid transcriptional activation of odc and other immediate early genes during serum stimulation. © 1994 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/jcb.240550202 |
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Although DNA methylation is generally associated with chromatin condensation and gene inactivation, the odc gene is heavily methylated at CCGG‐sequences in animal cell lines. In this work we analyzed the chromatin structure and the DNA methylation status at the CpG‐rich promoter sequences at the odc locus in mouse 3T3 fibroblasts. We show that the proximal promoter region of the odc locus is not hypermethylated, while the distal promoter sequences appear to have a few methylated CCGG‐sites and display methylation polymorphism. Furthermore, it was found that the 5′ promoter region of odc is constitutively more sensitive to micrococcal nuclease than the coding and 3′ regions of the odc gene. Stimulation of the cells with serum resulted in an appearance of a DNase I sensitive site at the promoter region. The chromatin structure of the mid‐coding and 3′ regions of the odc gene also underwent structural changes that were accompanied by the rapid accumulation of odc mRNA. Such changes were not detected in the chromatin structure of glyceraldehyde‐3‐phosphate dehydrogenase (gadph) gene, whose expression remains invariant upon serum stimulation. These data suggest that the chromatin structure may play an important role in the rapid transcriptional activation of odc and other immediate early genes during serum stimulation. © 1994 Wiley‐Liss, Inc.</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.240550202</identifier><identifier>PMID: 7522236</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>3T3 Cells - enzymology ; 3T3 Cells - ultrastructure ; Animals ; Base Sequence ; Binding Sites ; cell cycle ; Chromatin - ultrastructure ; chromatin structure ; Deoxyribonuclease HpaII ; Deoxyribonuclease I - metabolism ; Deoxyribonucleases, Type II Site-Specific - metabolism ; DNA - chemistry ; DNA - metabolism ; DNA methylation ; Exons ; Glyceraldehyde-3-Phosphate Dehydrogenases - genetics ; Methylation ; Mice ; Nucleic Acid Hybridization ; Ornithine Decarboxylase - genetics ; Promoter Regions, Genetic ; Regulatory Sequences, Nucleic Acid ; RNA, Messenger - metabolism ; serum stimulation ; transcription</subject><ispartof>Journal of cellular biochemistry, 1994-06, Vol.55 (2), p.155-167</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4052-9a63f7c7f04c928bba47f1bcdebd26615d89c4eda08c49d0b3ba348b0a98acd63</citedby><cites>FETCH-LOGICAL-c4052-9a63f7c7f04c928bba47f1bcdebd26615d89c4eda08c49d0b3ba348b0a98acd63</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%2Fjcb.240550202$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcb.240550202$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7522236$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Laitinen, Jens</creatorcontrib><creatorcontrib>Hölttä, Erkki</creatorcontrib><title>Methylation status and chromatin structure of an early response gene (ornithine decarboxylase) in resting and stimulated NIH-3T3 fibroblasts</title><title>Journal of cellular biochemistry</title><addtitle>J. Cell. Biochem</addtitle><description>The early response gene ornithine decarboxylase (odc) is indispensable for normal and malignant cell growth. Although DNA methylation is generally associated with chromatin condensation and gene inactivation, the odc gene is heavily methylated at CCGG‐sequences in animal cell lines. In this work we analyzed the chromatin structure and the DNA methylation status at the CpG‐rich promoter sequences at the odc locus in mouse 3T3 fibroblasts. We show that the proximal promoter region of the odc locus is not hypermethylated, while the distal promoter sequences appear to have a few methylated CCGG‐sites and display methylation polymorphism. Furthermore, it was found that the 5′ promoter region of odc is constitutively more sensitive to micrococcal nuclease than the coding and 3′ regions of the odc gene. Stimulation of the cells with serum resulted in an appearance of a DNase I sensitive site at the promoter region. The chromatin structure of the mid‐coding and 3′ regions of the odc gene also underwent structural changes that were accompanied by the rapid accumulation of odc mRNA. Such changes were not detected in the chromatin structure of glyceraldehyde‐3‐phosphate dehydrogenase (gadph) gene, whose expression remains invariant upon serum stimulation. These data suggest that the chromatin structure may play an important role in the rapid transcriptional activation of odc and other immediate early genes during serum stimulation. © 1994 Wiley‐Liss, Inc.</description><subject>3T3 Cells - enzymology</subject><subject>3T3 Cells - ultrastructure</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Binding Sites</subject><subject>cell cycle</subject><subject>Chromatin - ultrastructure</subject><subject>chromatin structure</subject><subject>Deoxyribonuclease HpaII</subject><subject>Deoxyribonuclease I - metabolism</subject><subject>Deoxyribonucleases, Type II Site-Specific - metabolism</subject><subject>DNA - chemistry</subject><subject>DNA - metabolism</subject><subject>DNA methylation</subject><subject>Exons</subject><subject>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</subject><subject>Methylation</subject><subject>Mice</subject><subject>Nucleic Acid Hybridization</subject><subject>Ornithine Decarboxylase - genetics</subject><subject>Promoter Regions, Genetic</subject><subject>Regulatory Sequences, Nucleic Acid</subject><subject>RNA, Messenger - metabolism</subject><subject>serum stimulation</subject><subject>transcription</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EKkvhyBHJJwSHlInt2PERVvQDlXIp9Gj5Y9JNycaLnYjuf-BH47KrFSc4WLZmHj8e6yXkZQ0nNQB7d-fdCRPQNMCAPSKLGrSqhBTiMVmA4lAxXrOn5FnOdwCgNWdH5Eg1jDEuF-TXZ5xW28FOfRxpnuw0Z2rHQP0qxXWpPhTT7Kc5IY1daVG0adjShHkTx4z0Fkekb2Ia-2nVl2NAb5OL98WZ8S0tgoIWz-0fbTmt5_IaBnp1cV7xa0673qXoCj3l5-RJZ4eML_b7Mfl6-vF6eV5dfjm7WL6_rHz5J6u0lbxTXnUgvGatc1aornY-oAtMyroJrfYCg4XWCx3AcWe5aB1Y3VofJD8mr3feTYo_5jKeWffZ4zDYEeOcjZKqBgHiv2AtdZlI6QJWO9CnmHPCzmxSv7Zpa2owDzGZEpM5xFT4V3vx7NYYDvQ-l9JXu_7PfsDtv2Xm0_LD3-b9JH2e8P5w06bvRiquGnNzdVbWqZDtzTez5L8BQGGv0w</recordid><startdate>199406</startdate><enddate>199406</enddate><creator>Laitinen, Jens</creator><creator>Hölttä, Erkki</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>7TM</scope><scope>7X8</scope></search><sort><creationdate>199406</creationdate><title>Methylation status and chromatin structure of an early response gene (ornithine decarboxylase) in resting and stimulated NIH-3T3 fibroblasts</title><author>Laitinen, Jens ; Hölttä, Erkki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4052-9a63f7c7f04c928bba47f1bcdebd26615d89c4eda08c49d0b3ba348b0a98acd63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>3T3 Cells - enzymology</topic><topic>3T3 Cells - ultrastructure</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Binding Sites</topic><topic>cell cycle</topic><topic>Chromatin - ultrastructure</topic><topic>chromatin structure</topic><topic>Deoxyribonuclease HpaII</topic><topic>Deoxyribonuclease I - metabolism</topic><topic>Deoxyribonucleases, Type II Site-Specific - metabolism</topic><topic>DNA - chemistry</topic><topic>DNA - metabolism</topic><topic>DNA methylation</topic><topic>Exons</topic><topic>Glyceraldehyde-3-Phosphate Dehydrogenases - genetics</topic><topic>Methylation</topic><topic>Mice</topic><topic>Nucleic Acid Hybridization</topic><topic>Ornithine Decarboxylase - genetics</topic><topic>Promoter Regions, Genetic</topic><topic>Regulatory Sequences, Nucleic Acid</topic><topic>RNA, Messenger - metabolism</topic><topic>serum stimulation</topic><topic>transcription</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laitinen, Jens</creatorcontrib><creatorcontrib>Hölttä, Erkki</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laitinen, Jens</au><au>Hölttä, Erkki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Methylation status and chromatin structure of an early response gene (ornithine decarboxylase) in resting and stimulated NIH-3T3 fibroblasts</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J. Cell. Biochem</addtitle><date>1994-06</date><risdate>1994</risdate><volume>55</volume><issue>2</issue><spage>155</spage><epage>167</epage><pages>155-167</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><abstract>The early response gene ornithine decarboxylase (odc) is indispensable for normal and malignant cell growth. Although DNA methylation is generally associated with chromatin condensation and gene inactivation, the odc gene is heavily methylated at CCGG‐sequences in animal cell lines. In this work we analyzed the chromatin structure and the DNA methylation status at the CpG‐rich promoter sequences at the odc locus in mouse 3T3 fibroblasts. We show that the proximal promoter region of the odc locus is not hypermethylated, while the distal promoter sequences appear to have a few methylated CCGG‐sites and display methylation polymorphism. Furthermore, it was found that the 5′ promoter region of odc is constitutively more sensitive to micrococcal nuclease than the coding and 3′ regions of the odc gene. Stimulation of the cells with serum resulted in an appearance of a DNase I sensitive site at the promoter region. The chromatin structure of the mid‐coding and 3′ regions of the odc gene also underwent structural changes that were accompanied by the rapid accumulation of odc mRNA. Such changes were not detected in the chromatin structure of glyceraldehyde‐3‐phosphate dehydrogenase (gadph) gene, whose expression remains invariant upon serum stimulation. These data suggest that the chromatin structure may play an important role in the rapid transcriptional activation of odc and other immediate early genes during serum stimulation. © 1994 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7522236</pmid><doi>10.1002/jcb.240550202</doi><tpages>13</tpages></addata></record> |
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subjects | 3T3 Cells - enzymology 3T3 Cells - ultrastructure Animals Base Sequence Binding Sites cell cycle Chromatin - ultrastructure chromatin structure Deoxyribonuclease HpaII Deoxyribonuclease I - metabolism Deoxyribonucleases, Type II Site-Specific - metabolism DNA - chemistry DNA - metabolism DNA methylation Exons Glyceraldehyde-3-Phosphate Dehydrogenases - genetics Methylation Mice Nucleic Acid Hybridization Ornithine Decarboxylase - genetics Promoter Regions, Genetic Regulatory Sequences, Nucleic Acid RNA, Messenger - metabolism serum stimulation transcription |
title | Methylation status and chromatin structure of an early response gene (ornithine decarboxylase) in resting and stimulated NIH-3T3 fibroblasts |
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