Conditional deletion of the colony stimulating factor-1 receptor (c-fms proto-oncogene) in mice
Colony stimulating factor‐1 (CSF‐1) is the primary regulator of the mononuclear phagocytic lineage acting through its transmembrane tyrosine kinase receptor, CSF‐1R, that is the product of the c‐fms proto‐oncogene. Null mutations in either the ligand or the receptor genes result in a severe osteopet...
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Veröffentlicht in: | Genesis (New York, N.Y. : 2000) N.Y. : 2000), 2006-07, Vol.44 (7), p.328-335 |
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creator | Li, Jia Chen, Ken Zhu, Liyin Pollard, Jeffrey W. |
description | Colony stimulating factor‐1 (CSF‐1) is the primary regulator of the mononuclear phagocytic lineage acting through its transmembrane tyrosine kinase receptor, CSF‐1R, that is the product of the c‐fms proto‐oncogene. Null mutations in either the ligand or the receptor genes result in a severe osteopetrosis as well as a number of other phenotypes, including reproductive defects and perturbations in organ development. The CSF‐1R is also expressed in oocytes, myoblast progenitors, decidual, and trophoblastic cells. To distinguish cell type specific phenotypes, we have created a conditional allele of the Csf1r by placing LoxP sites around Exon 5 of the Csf1r gene in mice. Excision of this floxed sequence results in a null allele that in the homozygous state gives a phenotype indistinguishable of the complete Csf1r null mutant mouse. This conditional allele will prove extremely valuable to study the spatial and temporal roles of CSF‐1R. genesis 44:328–335, 2006. © 2006 Wiley‐Liss, Inc. |
doi_str_mv | 10.1002/dvg.20219 |
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Null mutations in either the ligand or the receptor genes result in a severe osteopetrosis as well as a number of other phenotypes, including reproductive defects and perturbations in organ development. The CSF‐1R is also expressed in oocytes, myoblast progenitors, decidual, and trophoblastic cells. To distinguish cell type specific phenotypes, we have created a conditional allele of the Csf1r by placing LoxP sites around Exon 5 of the Csf1r gene in mice. Excision of this floxed sequence results in a null allele that in the homozygous state gives a phenotype indistinguishable of the complete Csf1r null mutant mouse. This conditional allele will prove extremely valuable to study the spatial and temporal roles of CSF‐1R. genesis 44:328–335, 2006. © 2006 Wiley‐Liss, Inc.</description><identifier>ISSN: 1526-954X</identifier><identifier>EISSN: 1526-968X</identifier><identifier>DOI: 10.1002/dvg.20219</identifier><identifier>PMID: 16823860</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animals ; CSF-1 ; Female ; Gene Targeting ; Genes, fms - genetics ; M-CSF ; Macrophage Colony-Stimulating Factor - metabolism ; macrophages ; Male ; Mice ; Mice, Knockout ; Mice, Transgenic ; Phenotype ; Receptors, Colony-Stimulating Factor - genetics ; reproduction ; Sequence Deletion</subject><ispartof>Genesis (New York, N.Y. : 2000), 2006-07, Vol.44 (7), p.328-335</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><rights>(c) 2006 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4989-c3e307d6a855b29001d734359bbf6b3569ea7134c712c348188e4ef70869249d3</citedby><cites>FETCH-LOGICAL-c4989-c3e307d6a855b29001d734359bbf6b3569ea7134c712c348188e4ef70869249d3</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%2Fdvg.20219$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fdvg.20219$$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/16823860$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Jia</creatorcontrib><creatorcontrib>Chen, Ken</creatorcontrib><creatorcontrib>Zhu, Liyin</creatorcontrib><creatorcontrib>Pollard, Jeffrey W.</creatorcontrib><title>Conditional deletion of the colony stimulating factor-1 receptor (c-fms proto-oncogene) in mice</title><title>Genesis (New York, N.Y. : 2000)</title><addtitle>Genesis</addtitle><description>Colony stimulating factor‐1 (CSF‐1) is the primary regulator of the mononuclear phagocytic lineage acting through its transmembrane tyrosine kinase receptor, CSF‐1R, that is the product of the c‐fms proto‐oncogene. Null mutations in either the ligand or the receptor genes result in a severe osteopetrosis as well as a number of other phenotypes, including reproductive defects and perturbations in organ development. The CSF‐1R is also expressed in oocytes, myoblast progenitors, decidual, and trophoblastic cells. To distinguish cell type specific phenotypes, we have created a conditional allele of the Csf1r by placing LoxP sites around Exon 5 of the Csf1r gene in mice. Excision of this floxed sequence results in a null allele that in the homozygous state gives a phenotype indistinguishable of the complete Csf1r null mutant mouse. This conditional allele will prove extremely valuable to study the spatial and temporal roles of CSF‐1R. genesis 44:328–335, 2006. © 2006 Wiley‐Liss, Inc.</description><subject>Animals</subject><subject>CSF-1</subject><subject>Female</subject><subject>Gene Targeting</subject><subject>Genes, fms - genetics</subject><subject>M-CSF</subject><subject>Macrophage Colony-Stimulating Factor - metabolism</subject><subject>macrophages</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Knockout</subject><subject>Mice, Transgenic</subject><subject>Phenotype</subject><subject>Receptors, Colony-Stimulating Factor - genetics</subject><subject>reproduction</subject><subject>Sequence Deletion</subject><issn>1526-954X</issn><issn>1526-968X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkEtP20AUhUeoFe8Ff6CaVVUWhnk_llUKKRJqN-GxG43H1-mA7Uk9TiH_vg4JsKq6umfxnU9XB6ETSs4oIey8-jM_Y4RRu4P2qWSqsMrcf3jNUtzvoYOcHwgh0jC2i_aoMowbRfaRm6SuikNMnW9wBQ2sI041Hn4BDqlJ3QrnIbbLxg-xm-PahyH1BcU9BFiMEX8JRd1mvOjTkIrUhTSHDk5x7HAbAxyhj7VvMhxv7yG6ubyYTb4X1z-nV5Ov10UQ1tgicOBEV8obKUtmCaGV5oJLW5a1KrlUFrymXARNWeDCUGNAQK2JUZYJW_FD9HnjHf_4vYQ8uDbmAE3jO0jL7JRRwhjF_wtSzYRkYg2ebsDQp5x7qN2ij63vV44St57djbO7l9lH9tNWuixbqN7J7c4jcL4BnmIDq3-b3Lfb6auy2DRiHuD5reH7R6c019Ld_Zi6yWxGtDCXTvK_toeaEw</recordid><startdate>200607</startdate><enddate>200607</enddate><creator>Li, Jia</creator><creator>Chen, Ken</creator><creator>Zhu, Liyin</creator><creator>Pollard, Jeffrey W.</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>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>200607</creationdate><title>Conditional deletion of the colony stimulating factor-1 receptor (c-fms proto-oncogene) in mice</title><author>Li, Jia ; Chen, Ken ; Zhu, Liyin ; Pollard, Jeffrey W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4989-c3e307d6a855b29001d734359bbf6b3569ea7134c712c348188e4ef70869249d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Animals</topic><topic>CSF-1</topic><topic>Female</topic><topic>Gene Targeting</topic><topic>Genes, fms - genetics</topic><topic>M-CSF</topic><topic>Macrophage Colony-Stimulating Factor - metabolism</topic><topic>macrophages</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Knockout</topic><topic>Mice, Transgenic</topic><topic>Phenotype</topic><topic>Receptors, Colony-Stimulating Factor - genetics</topic><topic>reproduction</topic><topic>Sequence Deletion</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Jia</creatorcontrib><creatorcontrib>Chen, Ken</creatorcontrib><creatorcontrib>Zhu, Liyin</creatorcontrib><creatorcontrib>Pollard, Jeffrey W.</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>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Genesis (New York, N.Y. : 2000)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Jia</au><au>Chen, Ken</au><au>Zhu, Liyin</au><au>Pollard, Jeffrey W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Conditional deletion of the colony stimulating factor-1 receptor (c-fms proto-oncogene) in mice</atitle><jtitle>Genesis (New York, N.Y. : 2000)</jtitle><addtitle>Genesis</addtitle><date>2006-07</date><risdate>2006</risdate><volume>44</volume><issue>7</issue><spage>328</spage><epage>335</epage><pages>328-335</pages><issn>1526-954X</issn><eissn>1526-968X</eissn><abstract>Colony stimulating factor‐1 (CSF‐1) is the primary regulator of the mononuclear phagocytic lineage acting through its transmembrane tyrosine kinase receptor, CSF‐1R, that is the product of the c‐fms proto‐oncogene. Null mutations in either the ligand or the receptor genes result in a severe osteopetrosis as well as a number of other phenotypes, including reproductive defects and perturbations in organ development. The CSF‐1R is also expressed in oocytes, myoblast progenitors, decidual, and trophoblastic cells. To distinguish cell type specific phenotypes, we have created a conditional allele of the Csf1r by placing LoxP sites around Exon 5 of the Csf1r gene in mice. Excision of this floxed sequence results in a null allele that in the homozygous state gives a phenotype indistinguishable of the complete Csf1r null mutant mouse. This conditional allele will prove extremely valuable to study the spatial and temporal roles of CSF‐1R. genesis 44:328–335, 2006. © 2006 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>16823860</pmid><doi>10.1002/dvg.20219</doi><tpages>8</tpages></addata></record> |
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subjects | Animals CSF-1 Female Gene Targeting Genes, fms - genetics M-CSF Macrophage Colony-Stimulating Factor - metabolism macrophages Male Mice Mice, Knockout Mice, Transgenic Phenotype Receptors, Colony-Stimulating Factor - genetics reproduction Sequence Deletion |
title | Conditional deletion of the colony stimulating factor-1 receptor (c-fms proto-oncogene) in mice |
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