Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10
Remodeling of the extracellular matrix (ECM) is an essential component of normal development and is also involved in the pathogenesis of arthritis and the spread of cancer. The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an import...
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Veröffentlicht in: | Developmental dynamics 1994-07, Vol.200 (3), p.177-197 |
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description | Remodeling of the extracellular matrix (ECM) is an essential component of normal development and is also involved in the pathogenesis of arthritis and the spread of cancer. The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an important role in this context. We have isolated mouse cDNA clones encoding a novel member of the TIMP family, designated TIMP‐3. We have assigned the Timp‐3 locus to the [C1–D1] region of mouse chromosome 10 using both genetic and cytogenetic methods. The conceptual translation product of the Timp‐3 cDNA shows a high degree of similarity with ChIMP‐3, a recently cloned chicken metalloproteinase inhibitor, as well as significant structural similarity with the amino acid sequences of the previously isolated members of this family, TIMP‐1 and TIMP‐2. The pattern of expression of Timp‐3 in the developing mouse embryo is distinct from that previously reported for Timp‐1. Timp‐3 is expressed in cartilage and skeletal muscle, in myocardium, in the skin, oral and nasal epithelium, in the newborn mouse liver, in the epithelium of some tubular structures such as the developing bronchial tree, oesophagus, colon, urogenital sinus, bile duct, in the kidney, salivary glands, and in the choroid plexus of the brain. The patterns of Timp‐3 expression in surface epithelia and in the epithelial lining of many tubular organs suggests that TIMP‐3 may be involved in regulating ECM remodeling during the folding of epithelia and during the formation, branching, and expansion of epithelial tubes. In the mouse placenta, expression is seen in the trophoblast, raising the possibility that TIMP‐3 may be involved in regulating trophoblastic invasion of the uterus. We propose a role for TIMP‐3 in musculoskeletal and cardiac development, in the morphogenesis of certain epithelial structures, and placental implantation. © 1994 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/aja.1002000302 |
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The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an important role in this context. We have isolated mouse cDNA clones encoding a novel member of the TIMP family, designated TIMP‐3. We have assigned the Timp‐3 locus to the [C1–D1] region of mouse chromosome 10 using both genetic and cytogenetic methods. The conceptual translation product of the Timp‐3 cDNA shows a high degree of similarity with ChIMP‐3, a recently cloned chicken metalloproteinase inhibitor, as well as significant structural similarity with the amino acid sequences of the previously isolated members of this family, TIMP‐1 and TIMP‐2. The pattern of expression of Timp‐3 in the developing mouse embryo is distinct from that previously reported for Timp‐1. Timp‐3 is expressed in cartilage and skeletal muscle, in myocardium, in the skin, oral and nasal epithelium, in the newborn mouse liver, in the epithelium of some tubular structures such as the developing bronchial tree, oesophagus, colon, urogenital sinus, bile duct, in the kidney, salivary glands, and in the choroid plexus of the brain. The patterns of Timp‐3 expression in surface epithelia and in the epithelial lining of many tubular organs suggests that TIMP‐3 may be involved in regulating ECM remodeling during the folding of epithelia and during the formation, branching, and expansion of epithelial tubes. In the mouse placenta, expression is seen in the trophoblast, raising the possibility that TIMP‐3 may be involved in regulating trophoblastic invasion of the uterus. We propose a role for TIMP‐3 in musculoskeletal and cardiac development, in the morphogenesis of certain epithelial structures, and placental implantation. © 1994 Wiley‐Liss, Inc.</description><identifier>ISSN: 1058-8388</identifier><identifier>EISSN: 1097-0177</identifier><identifier>DOI: 10.1002/aja.1002000302</identifier><identifier>PMID: 7949367</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Amino Acid Sequence ; Animals ; Animals, Newborn ; Base Sequence ; Blotting, Northern ; Cartilage ; Cartilage - embryology ; Cartilage - growth & development ; Cartilage - metabolism ; Chromosome Mapping ; Chromosomes - genetics ; Cloning, Molecular ; Embryo, Mammalian - metabolism ; Embryonic and Fetal Development ; Epithelium ; Epithelium - embryology ; Epithelium - growth & development ; Epithelium - metabolism ; Extracellular matrix ; Gene Expression ; In Situ Hybridization ; Metalloendopeptidases - antagonists & inhibitors ; Metalloproteinases ; Mice ; Molecular Sequence Data ; Muscle ; Muscle Development ; Muscles - embryology ; Muscles - metabolism ; Neoplasm Proteins - chemistry ; Neoplasm Proteins - genetics ; Placenta - metabolism ; TIMP‐3 ; Tissue Inhibitor of Metalloproteinase-3</subject><ispartof>Developmental dynamics, 1994-07, Vol.200 (3), p.177-197</ispartof><rights>Copyright © 1994 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4752-188294b85894c0a7d7e6695d7e15cac315627805308cd019d99e435d39e3074b3</citedby><cites>FETCH-LOGICAL-c4752-188294b85894c0a7d7e6695d7e15cac315627805308cd019d99e435d39e3074b3</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%2Faja.1002000302$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faja.1002000302$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/7949367$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Apte, Suneel S.</creatorcontrib><creatorcontrib>Hayashi, Kimiko</creatorcontrib><creatorcontrib>Seldin, Michael F.</creatorcontrib><creatorcontrib>Mattei, Marie‐Genevieve</creatorcontrib><creatorcontrib>Hayashi, Masando</creatorcontrib><creatorcontrib>Olsen, Bjorn R.</creatorcontrib><title>Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10</title><title>Developmental dynamics</title><addtitle>Dev Dyn</addtitle><description>Remodeling of the extracellular matrix (ECM) is an essential component of normal development and is also involved in the pathogenesis of arthritis and the spread of cancer. The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an important role in this context. We have isolated mouse cDNA clones encoding a novel member of the TIMP family, designated TIMP‐3. We have assigned the Timp‐3 locus to the [C1–D1] region of mouse chromosome 10 using both genetic and cytogenetic methods. The conceptual translation product of the Timp‐3 cDNA shows a high degree of similarity with ChIMP‐3, a recently cloned chicken metalloproteinase inhibitor, as well as significant structural similarity with the amino acid sequences of the previously isolated members of this family, TIMP‐1 and TIMP‐2. The pattern of expression of Timp‐3 in the developing mouse embryo is distinct from that previously reported for Timp‐1. Timp‐3 is expressed in cartilage and skeletal muscle, in myocardium, in the skin, oral and nasal epithelium, in the newborn mouse liver, in the epithelium of some tubular structures such as the developing bronchial tree, oesophagus, colon, urogenital sinus, bile duct, in the kidney, salivary glands, and in the choroid plexus of the brain. The patterns of Timp‐3 expression in surface epithelia and in the epithelial lining of many tubular organs suggests that TIMP‐3 may be involved in regulating ECM remodeling during the folding of epithelia and during the formation, branching, and expansion of epithelial tubes. In the mouse placenta, expression is seen in the trophoblast, raising the possibility that TIMP‐3 may be involved in regulating trophoblastic invasion of the uterus. We propose a role for TIMP‐3 in musculoskeletal and cardiac development, in the morphogenesis of certain epithelial structures, and placental implantation. © 1994 Wiley‐Liss, Inc.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Base Sequence</subject><subject>Blotting, Northern</subject><subject>Cartilage</subject><subject>Cartilage - embryology</subject><subject>Cartilage - growth & development</subject><subject>Cartilage - metabolism</subject><subject>Chromosome Mapping</subject><subject>Chromosomes - genetics</subject><subject>Cloning, Molecular</subject><subject>Embryo, Mammalian - metabolism</subject><subject>Embryonic and Fetal Development</subject><subject>Epithelium</subject><subject>Epithelium - embryology</subject><subject>Epithelium - growth & development</subject><subject>Epithelium - metabolism</subject><subject>Extracellular matrix</subject><subject>Gene Expression</subject><subject>In Situ Hybridization</subject><subject>Metalloendopeptidases - antagonists & inhibitors</subject><subject>Metalloproteinases</subject><subject>Mice</subject><subject>Molecular Sequence Data</subject><subject>Muscle</subject><subject>Muscle Development</subject><subject>Muscles - embryology</subject><subject>Muscles - metabolism</subject><subject>Neoplasm Proteins - chemistry</subject><subject>Neoplasm Proteins - genetics</subject><subject>Placenta - metabolism</subject><subject>TIMP‐3</subject><subject>Tissue Inhibitor of Metalloproteinase-3</subject><issn>1058-8388</issn><issn>1097-0177</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EKqVw7a2ST1WRNsWO49g-riooRa3KoZwjrz3bdeXYqZ209MYj8EQ8DE-Cl42AG6cZef75_rF-hA4pOaWE1O_0nf7dEEIYqZ-hfUqUqAgV4vm257KSTMqX6FXOd0Uj24buoT2hGsVasY9-nEMADMFE68It1jjEB_C4n5Ir76PLeQLswsat3BgTjmvcw6i9j0OKI7igM2R8cnNx9fntAm_Lz2_f2QK7jOHrkCBnsGUdWyjUOGwt-jjl4ji4cQPe6QU2Oo3O61tYYB1ssc7Gz33B-Gj0WCAxzJtmk2Ifc-wBU_IavVhrn-HNXA_Qlw_vb84-VpfX5xdny8vKNILXFZWyVs1KcqkaQ7SwAtpW8VIoN9owyttaSMIZkcYSqqxS0DBumQJGRLNiB-h4xy3fvp8gj13vsgHvdYByVSdaoQQndRGe7oQmxZwTrLshuV6np46SbptTVwLr_gZWFo5m8rTqwf6RzwmVudrNH52Hp__QuuWn5T_sX_bwoxU</recordid><startdate>199407</startdate><enddate>199407</enddate><creator>Apte, Suneel S.</creator><creator>Hayashi, Kimiko</creator><creator>Seldin, Michael F.</creator><creator>Mattei, Marie‐Genevieve</creator><creator>Hayashi, Masando</creator><creator>Olsen, Bjorn R.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><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>199407</creationdate><title>Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10</title><author>Apte, Suneel S. ; Hayashi, Kimiko ; Seldin, Michael F. ; Mattei, Marie‐Genevieve ; Hayashi, Masando ; Olsen, Bjorn R.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4752-188294b85894c0a7d7e6695d7e15cac315627805308cd019d99e435d39e3074b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Base Sequence</topic><topic>Blotting, Northern</topic><topic>Cartilage</topic><topic>Cartilage - embryology</topic><topic>Cartilage - growth & development</topic><topic>Cartilage - metabolism</topic><topic>Chromosome Mapping</topic><topic>Chromosomes - genetics</topic><topic>Cloning, Molecular</topic><topic>Embryo, Mammalian - metabolism</topic><topic>Embryonic and Fetal Development</topic><topic>Epithelium</topic><topic>Epithelium - embryology</topic><topic>Epithelium - growth & development</topic><topic>Epithelium - metabolism</topic><topic>Extracellular matrix</topic><topic>Gene Expression</topic><topic>In Situ Hybridization</topic><topic>Metalloendopeptidases - antagonists & inhibitors</topic><topic>Metalloproteinases</topic><topic>Mice</topic><topic>Molecular Sequence Data</topic><topic>Muscle</topic><topic>Muscle Development</topic><topic>Muscles - embryology</topic><topic>Muscles - metabolism</topic><topic>Neoplasm Proteins - chemistry</topic><topic>Neoplasm Proteins - genetics</topic><topic>Placenta - metabolism</topic><topic>TIMP‐3</topic><topic>Tissue Inhibitor of Metalloproteinase-3</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Apte, Suneel S.</creatorcontrib><creatorcontrib>Hayashi, Kimiko</creatorcontrib><creatorcontrib>Seldin, Michael F.</creatorcontrib><creatorcontrib>Mattei, Marie‐Genevieve</creatorcontrib><creatorcontrib>Hayashi, Masando</creatorcontrib><creatorcontrib>Olsen, Bjorn R.</creatorcontrib><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>Developmental dynamics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Apte, Suneel S.</au><au>Hayashi, Kimiko</au><au>Seldin, Michael F.</au><au>Mattei, Marie‐Genevieve</au><au>Hayashi, Masando</au><au>Olsen, Bjorn R.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10</atitle><jtitle>Developmental dynamics</jtitle><addtitle>Dev Dyn</addtitle><date>1994-07</date><risdate>1994</risdate><volume>200</volume><issue>3</issue><spage>177</spage><epage>197</epage><pages>177-197</pages><issn>1058-8388</issn><eissn>1097-0177</eissn><abstract>Remodeling of the extracellular matrix (ECM) is an essential component of normal development and is also involved in the pathogenesis of arthritis and the spread of cancer. The matrix metalloproteinases and their natural inhibitors, the tissue inhibitors of metalloproteinases (TIMPs), play an important role in this context. We have isolated mouse cDNA clones encoding a novel member of the TIMP family, designated TIMP‐3. We have assigned the Timp‐3 locus to the [C1–D1] region of mouse chromosome 10 using both genetic and cytogenetic methods. The conceptual translation product of the Timp‐3 cDNA shows a high degree of similarity with ChIMP‐3, a recently cloned chicken metalloproteinase inhibitor, as well as significant structural similarity with the amino acid sequences of the previously isolated members of this family, TIMP‐1 and TIMP‐2. The pattern of expression of Timp‐3 in the developing mouse embryo is distinct from that previously reported for Timp‐1. Timp‐3 is expressed in cartilage and skeletal muscle, in myocardium, in the skin, oral and nasal epithelium, in the newborn mouse liver, in the epithelium of some tubular structures such as the developing bronchial tree, oesophagus, colon, urogenital sinus, bile duct, in the kidney, salivary glands, and in the choroid plexus of the brain. The patterns of Timp‐3 expression in surface epithelia and in the epithelial lining of many tubular organs suggests that TIMP‐3 may be involved in regulating ECM remodeling during the folding of epithelia and during the formation, branching, and expansion of epithelial tubes. In the mouse placenta, expression is seen in the trophoblast, raising the possibility that TIMP‐3 may be involved in regulating trophoblastic invasion of the uterus. We propose a role for TIMP‐3 in musculoskeletal and cardiac development, in the morphogenesis of certain epithelial structures, and placental implantation. © 1994 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>7949367</pmid><doi>10.1002/aja.1002000302</doi><tpages>21</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amino Acid Sequence Animals Animals, Newborn Base Sequence Blotting, Northern Cartilage Cartilage - embryology Cartilage - growth & development Cartilage - metabolism Chromosome Mapping Chromosomes - genetics Cloning, Molecular Embryo, Mammalian - metabolism Embryonic and Fetal Development Epithelium Epithelium - embryology Epithelium - growth & development Epithelium - metabolism Extracellular matrix Gene Expression In Situ Hybridization Metalloendopeptidases - antagonists & inhibitors Metalloproteinases Mice Molecular Sequence Data Muscle Muscle Development Muscles - embryology Muscles - metabolism Neoplasm Proteins - chemistry Neoplasm Proteins - genetics Placenta - metabolism TIMP‐3 Tissue Inhibitor of Metalloproteinase-3 |
title | Gene encoding a novel murine tissue inhibitor of metalloproteinases (TIMP), TIMP‐3, is expressed in developing mouse epithelia, cartilage, and muscle, and is located on mouse chromosome 10 |
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