Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene
Fragile X syndrome (FXS) results from the loss of expression of the fragile X mental retardation ( FMR1 ) gene. Individuals affected by FXS experience many behavioral problems, including cognitive impairment, hyperactivity, social anxiety, and autistic-like behaviors. A mouse model of Fmr1 deficienc...
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Veröffentlicht in: | Behavioral neuroscience 2008-06, Vol.122 (3), p.710-715 |
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creator | Spencer, Corinne M Graham, Deanna F Yuva-Paylor, Lisa A Nelson, David L Paylor, Richard |
description | Fragile X syndrome (FXS) results from the loss of expression of the fragile X mental retardation (
FMR1
) gene. Individuals affected by FXS experience many behavioral problems, including cognitive impairment, hyperactivity, social anxiety, and autistic-like behaviors. A mouse model of
Fmr1
deficiency (
Fmr1
KO) exhibits several similar behavioral phenotypes, including alterations in social behavior. In an earlier study,
Fmr1
knockout mice carrying a yeast-artificial chromosome (YAC) transgene that overexpresses normal human FMRP (KOYAC) showed a correction or overcorrection of some behavioral responses, such as hyperactivity and anxiety-related responses. This report presents results from a study examining transgenic rescue of abnormal social responses in
Fmr1
KO mice. Relative to their wild-type (WT) littermates,
Fmr1
KO mice made more active social approaches to standard C57BL/6 partner mice in a direct social interaction test, a result consistent with a previous study. KOYAC mice showed fewer active approaches to partners than the WT or
Fmr1
KO littermates, indicating correction of this phenotype. This finding expands the number of murine behavioral responses caused by
Fmr1
deficiency and corrected by overexpression of human FMRP. |
doi_str_mv | 10.1037/0735-7044.122.3.710 |
format | Article |
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FMR1
) gene. Individuals affected by FXS experience many behavioral problems, including cognitive impairment, hyperactivity, social anxiety, and autistic-like behaviors. A mouse model of
Fmr1
deficiency (
Fmr1
KO) exhibits several similar behavioral phenotypes, including alterations in social behavior. In an earlier study,
Fmr1
knockout mice carrying a yeast-artificial chromosome (YAC) transgene that overexpresses normal human FMRP (KOYAC) showed a correction or overcorrection of some behavioral responses, such as hyperactivity and anxiety-related responses. This report presents results from a study examining transgenic rescue of abnormal social responses in
Fmr1
KO mice. Relative to their wild-type (WT) littermates,
Fmr1
KO mice made more active social approaches to standard C57BL/6 partner mice in a direct social interaction test, a result consistent with a previous study. KOYAC mice showed fewer active approaches to partners than the WT or
Fmr1
KO littermates, indicating correction of this phenotype. This finding expands the number of murine behavioral responses caused by
Fmr1
deficiency and corrected by overexpression of human FMRP.</description><identifier>ISSN: 0735-7044</identifier><identifier>EISSN: 1939-0084</identifier><identifier>DOI: 10.1037/0735-7044.122.3.710</identifier><identifier>PMID: 18513141</identifier><language>eng</language><publisher>United States: American Psychological Association</publisher><subject>Animal ; Animal Social Behavior ; Animals ; Anxiety ; Appetitive Behavior - physiology ; Artificial chromosomes ; Behavior, Animal - physiology ; Exploratory Behavior - physiology ; Fragile X Mental Retardation Protein - genetics ; Fragile X Syndrome ; Genes ; Genotype & phenotype ; Humans ; Intellectual disabilities ; Interpersonal Relations ; Locomotion - genetics ; Male ; Mice ; Mice, Inbred C57BL ; Mice, Transgenic - physiology ; Phenotype ; Rodents ; Social Interaction</subject><ispartof>Behavioral neuroscience, 2008-06, Vol.122 (3), p.710-715</ispartof><rights>2008 American Psychological Association</rights><rights>(Copyright) 2008 APA, all rights reserved.</rights><rights>Copyright American Psychological Association Jun 2008</rights><rights>2008, American Psychological Association</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a484t-2a8b7f7bcb99f1ca1e983707a62c63727a23d31be13000bad424f32ecd772c543</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18513141$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Spencer, Corinne M</creatorcontrib><creatorcontrib>Graham, Deanna F</creatorcontrib><creatorcontrib>Yuva-Paylor, Lisa A</creatorcontrib><creatorcontrib>Nelson, David L</creatorcontrib><creatorcontrib>Paylor, Richard</creatorcontrib><title>Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene</title><title>Behavioral neuroscience</title><addtitle>Behav Neurosci</addtitle><description>Fragile X syndrome (FXS) results from the loss of expression of the fragile X mental retardation (
FMR1
) gene. Individuals affected by FXS experience many behavioral problems, including cognitive impairment, hyperactivity, social anxiety, and autistic-like behaviors. A mouse model of
Fmr1
deficiency (
Fmr1
KO) exhibits several similar behavioral phenotypes, including alterations in social behavior. In an earlier study,
Fmr1
knockout mice carrying a yeast-artificial chromosome (YAC) transgene that overexpresses normal human FMRP (KOYAC) showed a correction or overcorrection of some behavioral responses, such as hyperactivity and anxiety-related responses. This report presents results from a study examining transgenic rescue of abnormal social responses in
Fmr1
KO mice. Relative to their wild-type (WT) littermates,
Fmr1
KO mice made more active social approaches to standard C57BL/6 partner mice in a direct social interaction test, a result consistent with a previous study. KOYAC mice showed fewer active approaches to partners than the WT or
Fmr1
KO littermates, indicating correction of this phenotype. This finding expands the number of murine behavioral responses caused by
Fmr1
deficiency and corrected by overexpression of human FMRP.</description><subject>Animal</subject><subject>Animal Social Behavior</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Appetitive Behavior - physiology</subject><subject>Artificial chromosomes</subject><subject>Behavior, Animal - physiology</subject><subject>Exploratory Behavior - physiology</subject><subject>Fragile X Mental Retardation Protein - genetics</subject><subject>Fragile X Syndrome</subject><subject>Genes</subject><subject>Genotype & phenotype</subject><subject>Humans</subject><subject>Intellectual disabilities</subject><subject>Interpersonal Relations</subject><subject>Locomotion - genetics</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic - physiology</subject><subject>Phenotype</subject><subject>Rodents</subject><subject>Social Interaction</subject><issn>0735-7044</issn><issn>1939-0084</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UtrGzEUBWARGmIn6S8oFFFoduPoSpqRtGxNXsSh0KRrcUfWuOPOw5E8Af_7yNgkIYtmpc2nw5EOIV-ATYAJdc6UyDPFpJwA5xMxUcAOyBiMMBljWn4i4xcxIscxLhljksn8iIxA5yBAwphc3Peuxob-9H_xqe4DrTt62Qagt13v_vXDmt7VztMphrCpuwVFej20mMzdb6APAbu48J0_JYcVNtF_3p8n5M_lxcP0Opv9urqZ_phlKLVcZxx1qSpVutKYChyCN1ooprDgrhCKK-RiLqD0IFLXEueSy0pw7-ZKcZdLcULOdrmr0D8OPq5tW0fnmwY73w_RKig4gGYfQjBF-kKuE_z2Di77IXTpEbYAKTVnufkf4kxoU5gCEhI75EIfY_CVXYW6xbCxwOx2MLudw27nsGkwK1LbbdGv--ihbP389c5-oQS-7wCu0K7ixmFY167x0ZadfxP0DPAimSQ</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>Spencer, Corinne M</creator><creator>Graham, Deanna F</creator><creator>Yuva-Paylor, Lisa A</creator><creator>Nelson, David L</creator><creator>Paylor, Richard</creator><general>American Psychological Association</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>7QG</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7RZ</scope><scope>PSYQQ</scope><scope>7QO</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20080601</creationdate><title>Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene</title><author>Spencer, Corinne M ; Graham, Deanna F ; Yuva-Paylor, Lisa A ; Nelson, David L ; Paylor, Richard</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a484t-2a8b7f7bcb99f1ca1e983707a62c63727a23d31be13000bad424f32ecd772c543</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animal</topic><topic>Animal Social Behavior</topic><topic>Animals</topic><topic>Anxiety</topic><topic>Appetitive Behavior - physiology</topic><topic>Artificial chromosomes</topic><topic>Behavior, Animal - physiology</topic><topic>Exploratory Behavior - physiology</topic><topic>Fragile X Mental Retardation Protein - genetics</topic><topic>Fragile X Syndrome</topic><topic>Genes</topic><topic>Genotype & phenotype</topic><topic>Humans</topic><topic>Intellectual disabilities</topic><topic>Interpersonal Relations</topic><topic>Locomotion - genetics</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic - physiology</topic><topic>Phenotype</topic><topic>Rodents</topic><topic>Social Interaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Spencer, Corinne M</creatorcontrib><creatorcontrib>Graham, Deanna F</creatorcontrib><creatorcontrib>Yuva-Paylor, Lisa A</creatorcontrib><creatorcontrib>Nelson, David L</creatorcontrib><creatorcontrib>Paylor, Richard</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>APA PsycArticles®</collection><collection>ProQuest One Psychology</collection><collection>Biotechnology Research Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Behavioral neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Spencer, Corinne M</au><au>Graham, Deanna F</au><au>Yuva-Paylor, Lisa A</au><au>Nelson, David L</au><au>Paylor, Richard</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene</atitle><jtitle>Behavioral neuroscience</jtitle><addtitle>Behav Neurosci</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>122</volume><issue>3</issue><spage>710</spage><epage>715</epage><pages>710-715</pages><issn>0735-7044</issn><eissn>1939-0084</eissn><abstract>Fragile X syndrome (FXS) results from the loss of expression of the fragile X mental retardation (
FMR1
) gene. Individuals affected by FXS experience many behavioral problems, including cognitive impairment, hyperactivity, social anxiety, and autistic-like behaviors. A mouse model of
Fmr1
deficiency (
Fmr1
KO) exhibits several similar behavioral phenotypes, including alterations in social behavior. In an earlier study,
Fmr1
knockout mice carrying a yeast-artificial chromosome (YAC) transgene that overexpresses normal human FMRP (KOYAC) showed a correction or overcorrection of some behavioral responses, such as hyperactivity and anxiety-related responses. This report presents results from a study examining transgenic rescue of abnormal social responses in
Fmr1
KO mice. Relative to their wild-type (WT) littermates,
Fmr1
KO mice made more active social approaches to standard C57BL/6 partner mice in a direct social interaction test, a result consistent with a previous study. KOYAC mice showed fewer active approaches to partners than the WT or
Fmr1
KO littermates, indicating correction of this phenotype. This finding expands the number of murine behavioral responses caused by
Fmr1
deficiency and corrected by overexpression of human FMRP.</abstract><cop>United States</cop><pub>American Psychological Association</pub><pmid>18513141</pmid><doi>10.1037/0735-7044.122.3.710</doi><tpages>6</tpages></addata></record> |
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source | APA PsycARTICLES; MEDLINE |
subjects | Animal Animal Social Behavior Animals Anxiety Appetitive Behavior - physiology Artificial chromosomes Behavior, Animal - physiology Exploratory Behavior - physiology Fragile X Mental Retardation Protein - genetics Fragile X Syndrome Genes Genotype & phenotype Humans Intellectual disabilities Interpersonal Relations Locomotion - genetics Male Mice Mice, Inbred C57BL Mice, Transgenic - physiology Phenotype Rodents Social Interaction |
title | Social Behavior in Fmr1 Knockout Mice Carrying a Human FMR1 Transgene |
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