The promoter of an androgen dependent gene in the hamster flank organ
Hamster flank organs are useful for studying androgen-dependent growth of hair follicles and sebaceous glands. A cDNA clone (FAR-17a) was isolated from the hamster flank organ, whose expression was highly sensitive to androgen. The mRNA level of this gene was reduced after castration but reappeared...
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Veröffentlicht in: | Journal of dermatological science 1997-05, Vol.15 (1), p.36-43 |
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creator | Aoki, Hirofumi Seki, Toshihiko Sawada, Junichi Handa, Hiroshi Adachi, Kenji |
description | Hamster flank organs are useful for studying androgen-dependent growth of hair follicles and sebaceous glands. A cDNA clone (FAR-17a) was isolated from the hamster flank organ, whose expression was highly sensitive to androgen. The mRNA level of this gene was reduced after castration but reappeared after testosterone treatment. To elucidate the mechanism of expression of this gene regulated by androgen we isolated a genomic clone, from a hamster genomic library, that includes the promoter and upsteam region. The promoter region was used to drive a luciferase reporter gene in Cos 7 cells. This construct was activated five to six times higher over a control plasmid lacking the promoter region. We tested the effects of testosterone by transfection of the reporter plasmid into androgen dependent SC-3 cells. The results showed up to fivefold stimulation after the addition of androgen. The sequence of this promoter region was analyzed and the transcription factor binding sites were predicted. Since no obvious androgen responsive elements were included in the promoter region, we suggest that the stimulation of the reporter construct has to be mediated indirectly by androgen-dependent transcription factor(s). |
doi_str_mv | 10.1016/S0923-1811(97)00597-5 |
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A cDNA clone (FAR-17a) was isolated from the hamster flank organ, whose expression was highly sensitive to androgen. The mRNA level of this gene was reduced after castration but reappeared after testosterone treatment. To elucidate the mechanism of expression of this gene regulated by androgen we isolated a genomic clone, from a hamster genomic library, that includes the promoter and upsteam region. The promoter region was used to drive a luciferase reporter gene in Cos 7 cells. This construct was activated five to six times higher over a control plasmid lacking the promoter region. We tested the effects of testosterone by transfection of the reporter plasmid into androgen dependent SC-3 cells. The results showed up to fivefold stimulation after the addition of androgen. The sequence of this promoter region was analyzed and the transcription factor binding sites were predicted. Since no obvious androgen responsive elements were included in the promoter region, we suggest that the stimulation of the reporter construct has to be mediated indirectly by androgen-dependent transcription factor(s).</description><identifier>ISSN: 0923-1811</identifier><identifier>EISSN: 1873-569X</identifier><identifier>DOI: 10.1016/S0923-1811(97)00597-5</identifier><identifier>PMID: 9186810</identifier><language>eng</language><publisher>Netherlands: Elsevier Ireland Ltd</publisher><subject>Amino Acid Sequence ; Androgen ; Androgens - physiology ; Animals ; Base Sequence ; Cricetinae - genetics ; FAR-17a ; Flank organ ; Genes ; Hair Follicle - physiology ; Hamster ; Mesocricetus ; Molecular Sequence Data ; Promoter ; Promoter Regions, Genetic ; Sebaceous Glands - physiology ; Transcription, Genetic</subject><ispartof>Journal of dermatological science, 1997-05, Vol.15 (1), p.36-43</ispartof><rights>1997</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c389t-7438186e4a0c703868bf0faa9716c86d8db8146bbf4d49c2bda53568676ce8763</citedby><cites>FETCH-LOGICAL-c389t-7438186e4a0c703868bf0faa9716c86d8db8146bbf4d49c2bda53568676ce8763</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0923181197005975$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9186810$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Aoki, Hirofumi</creatorcontrib><creatorcontrib>Seki, Toshihiko</creatorcontrib><creatorcontrib>Sawada, Junichi</creatorcontrib><creatorcontrib>Handa, Hiroshi</creatorcontrib><creatorcontrib>Adachi, Kenji</creatorcontrib><title>The promoter of an androgen dependent gene in the hamster flank organ</title><title>Journal of dermatological science</title><addtitle>J Dermatol Sci</addtitle><description>Hamster flank organs are useful for studying androgen-dependent growth of hair follicles and sebaceous glands. A cDNA clone (FAR-17a) was isolated from the hamster flank organ, whose expression was highly sensitive to androgen. The mRNA level of this gene was reduced after castration but reappeared after testosterone treatment. To elucidate the mechanism of expression of this gene regulated by androgen we isolated a genomic clone, from a hamster genomic library, that includes the promoter and upsteam region. The promoter region was used to drive a luciferase reporter gene in Cos 7 cells. This construct was activated five to six times higher over a control plasmid lacking the promoter region. We tested the effects of testosterone by transfection of the reporter plasmid into androgen dependent SC-3 cells. The results showed up to fivefold stimulation after the addition of androgen. The sequence of this promoter region was analyzed and the transcription factor binding sites were predicted. Since no obvious androgen responsive elements were included in the promoter region, we suggest that the stimulation of the reporter construct has to be mediated indirectly by androgen-dependent transcription factor(s).</description><subject>Amino Acid Sequence</subject><subject>Androgen</subject><subject>Androgens - physiology</subject><subject>Animals</subject><subject>Base Sequence</subject><subject>Cricetinae - genetics</subject><subject>FAR-17a</subject><subject>Flank organ</subject><subject>Genes</subject><subject>Hair Follicle - physiology</subject><subject>Hamster</subject><subject>Mesocricetus</subject><subject>Molecular Sequence Data</subject><subject>Promoter</subject><subject>Promoter Regions, Genetic</subject><subject>Sebaceous Glands - physiology</subject><subject>Transcription, Genetic</subject><issn>0923-1811</issn><issn>1873-569X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1LAzEQhoMotVZ_QiEn0cNq0t18nURK_YCCByt4C9lktl3tZmuyFfz3ZtviVQiEMM_knXkQGlNyQwnlt69ETfKMSkqvlLgmhCmRsSM0pFLkGePq_RgN_5BTdBbjB0nUpFADNFBUcknJEM0WK8Cb0DZtBwG3FTY-HRfaJXjsYAPege9wegGuPe4SvTJN7OFqbfwnbsPS-HN0Upl1hIvDPUJvD7PF9Cmbvzw-T-_nmc2l6jJR5DIFQ2GIFSRPI5QVqYxRgnIruZOulLTgZVkVrlB2UjrDcsYlF9yCFDwfocv9v2niry3ETjd1tLBOk0C7jVqopIEJlkC2B21oYwxQ6U2oGxN-NCW616d3-nTvRiuhd_p03zc-BGzLBtxf18FXqt_t65C2_K4h6Ghr8BZcHcB22rX1Pwm_osV-gQ</recordid><startdate>19970501</startdate><enddate>19970501</enddate><creator>Aoki, Hirofumi</creator><creator>Seki, Toshihiko</creator><creator>Sawada, Junichi</creator><creator>Handa, Hiroshi</creator><creator>Adachi, Kenji</creator><general>Elsevier Ireland Ltd</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>19970501</creationdate><title>The promoter of an androgen dependent gene in the hamster flank organ</title><author>Aoki, Hirofumi ; Seki, Toshihiko ; Sawada, Junichi ; Handa, Hiroshi ; Adachi, Kenji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c389t-7438186e4a0c703868bf0faa9716c86d8db8146bbf4d49c2bda53568676ce8763</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Amino Acid Sequence</topic><topic>Androgen</topic><topic>Androgens - physiology</topic><topic>Animals</topic><topic>Base Sequence</topic><topic>Cricetinae - genetics</topic><topic>FAR-17a</topic><topic>Flank organ</topic><topic>Genes</topic><topic>Hair Follicle - physiology</topic><topic>Hamster</topic><topic>Mesocricetus</topic><topic>Molecular Sequence Data</topic><topic>Promoter</topic><topic>Promoter Regions, Genetic</topic><topic>Sebaceous Glands - physiology</topic><topic>Transcription, Genetic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Aoki, Hirofumi</creatorcontrib><creatorcontrib>Seki, Toshihiko</creatorcontrib><creatorcontrib>Sawada, Junichi</creatorcontrib><creatorcontrib>Handa, Hiroshi</creatorcontrib><creatorcontrib>Adachi, Kenji</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>Journal of dermatological science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Aoki, Hirofumi</au><au>Seki, Toshihiko</au><au>Sawada, Junichi</au><au>Handa, Hiroshi</au><au>Adachi, Kenji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The promoter of an androgen dependent gene in the hamster flank organ</atitle><jtitle>Journal of dermatological science</jtitle><addtitle>J Dermatol Sci</addtitle><date>1997-05-01</date><risdate>1997</risdate><volume>15</volume><issue>1</issue><spage>36</spage><epage>43</epage><pages>36-43</pages><issn>0923-1811</issn><eissn>1873-569X</eissn><abstract>Hamster flank organs are useful for studying androgen-dependent growth of hair follicles and sebaceous glands. A cDNA clone (FAR-17a) was isolated from the hamster flank organ, whose expression was highly sensitive to androgen. The mRNA level of this gene was reduced after castration but reappeared after testosterone treatment. To elucidate the mechanism of expression of this gene regulated by androgen we isolated a genomic clone, from a hamster genomic library, that includes the promoter and upsteam region. The promoter region was used to drive a luciferase reporter gene in Cos 7 cells. This construct was activated five to six times higher over a control plasmid lacking the promoter region. We tested the effects of testosterone by transfection of the reporter plasmid into androgen dependent SC-3 cells. The results showed up to fivefold stimulation after the addition of androgen. The sequence of this promoter region was analyzed and the transcription factor binding sites were predicted. Since no obvious androgen responsive elements were included in the promoter region, we suggest that the stimulation of the reporter construct has to be mediated indirectly by androgen-dependent transcription factor(s).</abstract><cop>Netherlands</cop><pub>Elsevier Ireland Ltd</pub><pmid>9186810</pmid><doi>10.1016/S0923-1811(97)00597-5</doi><tpages>8</tpages></addata></record> |
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subjects | Amino Acid Sequence Androgen Androgens - physiology Animals Base Sequence Cricetinae - genetics FAR-17a Flank organ Genes Hair Follicle - physiology Hamster Mesocricetus Molecular Sequence Data Promoter Promoter Regions, Genetic Sebaceous Glands - physiology Transcription, Genetic |
title | The promoter of an androgen dependent gene in the hamster flank organ |
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