Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder

To expand, analyze and extend published behavioral phenotypes relevant to autism spectrum disorder (ASD), we present a study of three ASD genetic mouse models: Feng's Shank3tm2Gfng model, hereafter Shank3/F, Jiang's Shank3tm1Yhj model, hereafter Shank3/J and the Cacna1c deletion model. The...

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Veröffentlicht in:Genes, brain and behavior brain and behavior, 2018-01, Vol.17 (1), p.4-22
Hauptverfasser: Kabitzke, P.A., Brunner, D., He, D., Fazio, P.A., Cox, K., Sutphen, J., Thiede, L., Sabath, E., Hanania, T., Alexandrov, V., Rasmusson, R., Spooren, W., Ghosh, A., Feliciano, P., Biemans, B., Benedetti, M., Clayton, A.L.
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container_issue 1
container_start_page 4
container_title Genes, brain and behavior
container_volume 17
creator Kabitzke, P.A.
Brunner, D.
He, D.
Fazio, P.A.
Cox, K.
Sutphen, J.
Thiede, L.
Sabath, E.
Hanania, T.
Alexandrov, V.
Rasmusson, R.
Spooren, W.
Ghosh, A.
Feliciano, P.
Biemans, B.
Benedetti, M.
Clayton, A.L.
description To expand, analyze and extend published behavioral phenotypes relevant to autism spectrum disorder (ASD), we present a study of three ASD genetic mouse models: Feng's Shank3tm2Gfng model, hereafter Shank3/F, Jiang's Shank3tm1Yhj model, hereafter Shank3/J and the Cacna1c deletion model. The Shank3 models mimick gene mutations associated with Phelan–McDermid Syndrome and the Cacna1c model recapitulates the deletion underlying Timothy syndrome. This study utilizes both standard and novel behavioral tests with the same methodology used in our previously published companion report on the Cntnap2 null and 16p11.2 deletion models. We found that some but not all behaviors replicated published findings and those that did replicate, such as social behavior and overgrooming in Shank3 models, tended to be milder than reported elsewhere. The Shank3/F model, and to a much lesser extent, the Shank3/J and Cacna1c models, showed hypoactivity and a general anxiety‐like behavior triggered by external stimuli which pervaded social interactions. We did not detect deficits in a cognitive procedural learning test nor did we observe perseverative behavior in these models. We did, however, find differences in exploratory patterns of Cacna1c mutant mice suggestive of a behavioral effect in a social setting. In addition, only Shank3/F showed differences in sensory‐gating. Both positive and negative results from this study will be useful in identifying the most robust and replicable behavioral signatures within and across mouse models of autism. Understanding these phenotypes may shed light of which features to study when screening compounds for potential therapeutic interventions. SmartCube found different degrees of separation between mutant Shank3/F, Shank3/J mice and Cacna1c mice as compared with their corresponding WT control littermates. As described previously in detail (Brunner et al. 2015), to build a 2D representation of the multidimensional space in which the two groups are best separated, we first find statistically independent combinations of the original features, pick the two new composite features that best discriminate between the two groups, and used them as x‐ and y‐axes (drf 1 and 2; see Appendix Error! Reference source not found.). Each dot represents either a WT (blue) or a mutant (red) mouse. The center, small and large ellipses are the mean, standard error and standard deviation of the composite features for each group. The overlap between the groups is used t
doi_str_mv 10.1111/gbb.12405
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The Shank3 models mimick gene mutations associated with Phelan–McDermid Syndrome and the Cacna1c model recapitulates the deletion underlying Timothy syndrome. This study utilizes both standard and novel behavioral tests with the same methodology used in our previously published companion report on the Cntnap2 null and 16p11.2 deletion models. We found that some but not all behaviors replicated published findings and those that did replicate, such as social behavior and overgrooming in Shank3 models, tended to be milder than reported elsewhere. The Shank3/F model, and to a much lesser extent, the Shank3/J and Cacna1c models, showed hypoactivity and a general anxiety‐like behavior triggered by external stimuli which pervaded social interactions. We did not detect deficits in a cognitive procedural learning test nor did we observe perseverative behavior in these models. We did, however, find differences in exploratory patterns of Cacna1c mutant mice suggestive of a behavioral effect in a social setting. In addition, only Shank3/F showed differences in sensory‐gating. Both positive and negative results from this study will be useful in identifying the most robust and replicable behavioral signatures within and across mouse models of autism. Understanding these phenotypes may shed light of which features to study when screening compounds for potential therapeutic interventions. SmartCube found different degrees of separation between mutant Shank3/F, Shank3/J mice and Cacna1c mice as compared with their corresponding WT control littermates. As described previously in detail (Brunner et al. 2015), to build a 2D representation of the multidimensional space in which the two groups are best separated, we first find statistically independent combinations of the original features, pick the two new composite features that best discriminate between the two groups, and used them as x‐ and y‐axes (drf 1 and 2; see Appendix Error! Reference source not found.). Each dot represents either a WT (blue) or a mutant (red) mouse. The center, small and large ellipses are the mean, standard error and standard deviation of the composite features for each group. The overlap between the groups is used to calculate the discrimination index, which measures how reliably a classifier can be trained to discriminate between the two groups (the more overlap, the worse the discrimination). (a) The Shank3/F model separates well from the WT group. Note the spread and position variability of the individual mice. (b) The Shank3/J standard deviation ellipse overlaps considerably with the WT control ellipse. (c) The Cacna1c model separates well from the WT group. Note the spread and position variability of the individual mice. n = 13–16 mice per genotype/line.</description><identifier>ISSN: 1601-1848</identifier><identifier>EISSN: 1601-183X</identifier><identifier>DOI: 10.1111/gbb.12405</identifier><identifier>PMID: 28753255</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Animal models ; Animals ; Anxiety ; Anxiety - genetics ; Anxiety - metabolism ; Autism ; Autism Spectrum Disorder - genetics ; Autism Spectrum Disorder - metabolism ; Autistic Disorder - genetics ; Behavior ; Behavior, Animal - physiology ; Cacna1c ; Calcium Channels, L-Type - genetics ; Calcium Channels, L-Type - metabolism ; Chromosome Deletion ; Chromosome Disorders - genetics ; Chromosomes, Human, Pair 22 - genetics ; Cognitive ability ; development ; Disease Models, Animal ; External stimuli ; Female ; Gating ; Gene deletion ; Long QT Syndrome - genetics ; Male ; Mice ; Mice, Inbred C57BL ; mouse genetic models ; Mutation ; Nerve Tissue Proteins - genetics ; Nerve Tissue Proteins - metabolism ; Phelan‐McDermid syndrome ; phenotyping ; replication ; Sensory evaluation ; Shank3 ; Social Behavior ; Social interactions ; Syndactyly - genetics ; Therapeutic applications ; Timothy syndrome</subject><ispartof>Genes, brain and behavior, 2018-01, Vol.17 (1), p.4-22</ispartof><rights>2017 John Wiley &amp; Sons Ltd and International Behavioural and Neural Genetics Society</rights><rights>2017 John Wiley &amp; Sons Ltd and International Behavioural and Neural Genetics Society.</rights><rights>2018 John Wiley &amp; Sons Ltd and International Behavioural and Neural Genetics Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-31cab305cdd28793ff5b53b45011fcaed1d17fc19ecd594bbf0f9b52639b49813</citedby><cites>FETCH-LOGICAL-c3535-31cab305cdd28793ff5b53b45011fcaed1d17fc19ecd594bbf0f9b52639b49813</cites><orcidid>0000-0003-3305-0795</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fgbb.12405$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fgbb.12405$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,11541,27901,27902,45550,45551,46027,46451</link.rule.ids><linktorsrc>$$Uhttps://onlinelibrary.wiley.com/doi/abs/10.1111%2Fgbb.12405$$EView_record_in_Wiley-Blackwell$$FView_record_in_$$GWiley-Blackwell</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28753255$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kabitzke, P.A.</creatorcontrib><creatorcontrib>Brunner, D.</creatorcontrib><creatorcontrib>He, D.</creatorcontrib><creatorcontrib>Fazio, P.A.</creatorcontrib><creatorcontrib>Cox, K.</creatorcontrib><creatorcontrib>Sutphen, J.</creatorcontrib><creatorcontrib>Thiede, L.</creatorcontrib><creatorcontrib>Sabath, E.</creatorcontrib><creatorcontrib>Hanania, T.</creatorcontrib><creatorcontrib>Alexandrov, V.</creatorcontrib><creatorcontrib>Rasmusson, R.</creatorcontrib><creatorcontrib>Spooren, W.</creatorcontrib><creatorcontrib>Ghosh, A.</creatorcontrib><creatorcontrib>Feliciano, P.</creatorcontrib><creatorcontrib>Biemans, B.</creatorcontrib><creatorcontrib>Benedetti, M.</creatorcontrib><creatorcontrib>Clayton, A.L.</creatorcontrib><title>Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder</title><title>Genes, brain and behavior</title><addtitle>Genes Brain Behav</addtitle><description>To expand, analyze and extend published behavioral phenotypes relevant to autism spectrum disorder (ASD), we present a study of three ASD genetic mouse models: Feng's Shank3tm2Gfng model, hereafter Shank3/F, Jiang's Shank3tm1Yhj model, hereafter Shank3/J and the Cacna1c deletion model. The Shank3 models mimick gene mutations associated with Phelan–McDermid Syndrome and the Cacna1c model recapitulates the deletion underlying Timothy syndrome. This study utilizes both standard and novel behavioral tests with the same methodology used in our previously published companion report on the Cntnap2 null and 16p11.2 deletion models. We found that some but not all behaviors replicated published findings and those that did replicate, such as social behavior and overgrooming in Shank3 models, tended to be milder than reported elsewhere. The Shank3/F model, and to a much lesser extent, the Shank3/J and Cacna1c models, showed hypoactivity and a general anxiety‐like behavior triggered by external stimuli which pervaded social interactions. We did not detect deficits in a cognitive procedural learning test nor did we observe perseverative behavior in these models. We did, however, find differences in exploratory patterns of Cacna1c mutant mice suggestive of a behavioral effect in a social setting. In addition, only Shank3/F showed differences in sensory‐gating. Both positive and negative results from this study will be useful in identifying the most robust and replicable behavioral signatures within and across mouse models of autism. Understanding these phenotypes may shed light of which features to study when screening compounds for potential therapeutic interventions. SmartCube found different degrees of separation between mutant Shank3/F, Shank3/J mice and Cacna1c mice as compared with their corresponding WT control littermates. As described previously in detail (Brunner et al. 2015), to build a 2D representation of the multidimensional space in which the two groups are best separated, we first find statistically independent combinations of the original features, pick the two new composite features that best discriminate between the two groups, and used them as x‐ and y‐axes (drf 1 and 2; see Appendix Error! Reference source not found.). Each dot represents either a WT (blue) or a mutant (red) mouse. The center, small and large ellipses are the mean, standard error and standard deviation of the composite features for each group. The overlap between the groups is used to calculate the discrimination index, which measures how reliably a classifier can be trained to discriminate between the two groups (the more overlap, the worse the discrimination). (a) The Shank3/F model separates well from the WT group. Note the spread and position variability of the individual mice. (b) The Shank3/J standard deviation ellipse overlaps considerably with the WT control ellipse. (c) The Cacna1c model separates well from the WT group. Note the spread and position variability of the individual mice. n = 13–16 mice per genotype/line.</description><subject>Animal models</subject><subject>Animals</subject><subject>Anxiety</subject><subject>Anxiety - genetics</subject><subject>Anxiety - metabolism</subject><subject>Autism</subject><subject>Autism Spectrum Disorder - genetics</subject><subject>Autism Spectrum Disorder - metabolism</subject><subject>Autistic Disorder - genetics</subject><subject>Behavior</subject><subject>Behavior, Animal - physiology</subject><subject>Cacna1c</subject><subject>Calcium Channels, L-Type - genetics</subject><subject>Calcium Channels, L-Type - metabolism</subject><subject>Chromosome Deletion</subject><subject>Chromosome Disorders - genetics</subject><subject>Chromosomes, Human, Pair 22 - genetics</subject><subject>Cognitive ability</subject><subject>development</subject><subject>Disease Models, Animal</subject><subject>External stimuli</subject><subject>Female</subject><subject>Gating</subject><subject>Gene deletion</subject><subject>Long QT Syndrome - genetics</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>mouse genetic models</subject><subject>Mutation</subject><subject>Nerve Tissue Proteins - genetics</subject><subject>Nerve Tissue Proteins - metabolism</subject><subject>Phelan‐McDermid syndrome</subject><subject>phenotyping</subject><subject>replication</subject><subject>Sensory evaluation</subject><subject>Shank3</subject><subject>Social Behavior</subject><subject>Social interactions</subject><subject>Syndactyly - genetics</subject><subject>Therapeutic applications</subject><subject>Timothy syndrome</subject><issn>1601-1848</issn><issn>1601-183X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10MtKAzEUBuAgitXqwheQgBtdtOZMJu1kaYs3EFyo4EaGXE7s6FxqMqP07Y1t7UIwiySEj5-Tn5AjYEOI6_xV6yEkKRNbZA9GDAaQ8eftzT3NemQ_hDfGYMwz2CW9JBsLngixR16mTTX3OMM6FJ9IVa3KRSgCbRxtvxr6MFP1O4_PlrYzpFNlagWGVk0XMO4WyyVVXVuEioY5mtZ3FbVFaLxFf0B2nCoDHq7PPnm6unyc3gzu7q9vpxd3A8MFFwMORmnOhLE2Tia5c0ILrlPBAJxRaMHC2BmQaKyQqdaOOalFMuJSpzID3ienq9y5bz46DG1eFcFgWaoa46g5yCQVksk0jfTkD31rOh-__aMkMJGwEYvqbKWMb0Lw6PK5LyrlFzmw_KfzPHaeLzuP9nid2OkK7Ub-lhzB-Qp8FSUu_k_KryeTVeQ3t4yKUg</recordid><startdate>201801</startdate><enddate>201801</enddate><creator>Kabitzke, P.A.</creator><creator>Brunner, D.</creator><creator>He, D.</creator><creator>Fazio, P.A.</creator><creator>Cox, K.</creator><creator>Sutphen, J.</creator><creator>Thiede, L.</creator><creator>Sabath, E.</creator><creator>Hanania, T.</creator><creator>Alexandrov, V.</creator><creator>Rasmusson, R.</creator><creator>Spooren, W.</creator><creator>Ghosh, A.</creator><creator>Feliciano, P.</creator><creator>Biemans, B.</creator><creator>Benedetti, M.</creator><creator>Clayton, A.L.</creator><general>Blackwell Publishing Ltd</general><general>John Wiley &amp; Sons, Inc</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>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3305-0795</orcidid></search><sort><creationdate>201801</creationdate><title>Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder</title><author>Kabitzke, P.A. ; Brunner, D. ; He, D. ; Fazio, P.A. ; Cox, K. ; Sutphen, J. ; Thiede, L. ; Sabath, E. ; Hanania, T. ; Alexandrov, V. ; Rasmusson, R. ; Spooren, W. ; Ghosh, A. ; Feliciano, P. ; Biemans, B. ; Benedetti, M. ; Clayton, A.L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-31cab305cdd28793ff5b53b45011fcaed1d17fc19ecd594bbf0f9b52639b49813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Anxiety</topic><topic>Anxiety - 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Academic</collection><jtitle>Genes, brain and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Kabitzke, P.A.</au><au>Brunner, D.</au><au>He, D.</au><au>Fazio, P.A.</au><au>Cox, K.</au><au>Sutphen, J.</au><au>Thiede, L.</au><au>Sabath, E.</au><au>Hanania, T.</au><au>Alexandrov, V.</au><au>Rasmusson, R.</au><au>Spooren, W.</au><au>Ghosh, A.</au><au>Feliciano, P.</au><au>Biemans, B.</au><au>Benedetti, M.</au><au>Clayton, A.L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder</atitle><jtitle>Genes, brain and behavior</jtitle><addtitle>Genes Brain Behav</addtitle><date>2018-01</date><risdate>2018</risdate><volume>17</volume><issue>1</issue><spage>4</spage><epage>22</epage><pages>4-22</pages><issn>1601-1848</issn><eissn>1601-183X</eissn><abstract>To expand, analyze and extend published behavioral phenotypes relevant to autism spectrum disorder (ASD), we present a study of three ASD genetic mouse models: Feng's Shank3tm2Gfng model, hereafter Shank3/F, Jiang's Shank3tm1Yhj model, hereafter Shank3/J and the Cacna1c deletion model. The Shank3 models mimick gene mutations associated with Phelan–McDermid Syndrome and the Cacna1c model recapitulates the deletion underlying Timothy syndrome. This study utilizes both standard and novel behavioral tests with the same methodology used in our previously published companion report on the Cntnap2 null and 16p11.2 deletion models. We found that some but not all behaviors replicated published findings and those that did replicate, such as social behavior and overgrooming in Shank3 models, tended to be milder than reported elsewhere. The Shank3/F model, and to a much lesser extent, the Shank3/J and Cacna1c models, showed hypoactivity and a general anxiety‐like behavior triggered by external stimuli which pervaded social interactions. We did not detect deficits in a cognitive procedural learning test nor did we observe perseverative behavior in these models. We did, however, find differences in exploratory patterns of Cacna1c mutant mice suggestive of a behavioral effect in a social setting. In addition, only Shank3/F showed differences in sensory‐gating. Both positive and negative results from this study will be useful in identifying the most robust and replicable behavioral signatures within and across mouse models of autism. Understanding these phenotypes may shed light of which features to study when screening compounds for potential therapeutic interventions. SmartCube found different degrees of separation between mutant Shank3/F, Shank3/J mice and Cacna1c mice as compared with their corresponding WT control littermates. As described previously in detail (Brunner et al. 2015), to build a 2D representation of the multidimensional space in which the two groups are best separated, we first find statistically independent combinations of the original features, pick the two new composite features that best discriminate between the two groups, and used them as x‐ and y‐axes (drf 1 and 2; see Appendix Error! Reference source not found.). Each dot represents either a WT (blue) or a mutant (red) mouse. The center, small and large ellipses are the mean, standard error and standard deviation of the composite features for each group. The overlap between the groups is used to calculate the discrimination index, which measures how reliably a classifier can be trained to discriminate between the two groups (the more overlap, the worse the discrimination). (a) The Shank3/F model separates well from the WT group. Note the spread and position variability of the individual mice. (b) The Shank3/J standard deviation ellipse overlaps considerably with the WT control ellipse. (c) The Cacna1c model separates well from the WT group. Note the spread and position variability of the individual mice. n = 13–16 mice per genotype/line.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>28753255</pmid><doi>10.1111/gbb.12405</doi><tpages>19</tpages><orcidid>https://orcid.org/0000-0003-3305-0795</orcidid></addata></record>
fulltext fulltext_linktorsrc
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ispartof Genes, brain and behavior, 2018-01, Vol.17 (1), p.4-22
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source Wiley Online Library Open Access
subjects Animal models
Animals
Anxiety
Anxiety - genetics
Anxiety - metabolism
Autism
Autism Spectrum Disorder - genetics
Autism Spectrum Disorder - metabolism
Autistic Disorder - genetics
Behavior
Behavior, Animal - physiology
Cacna1c
Calcium Channels, L-Type - genetics
Calcium Channels, L-Type - metabolism
Chromosome Deletion
Chromosome Disorders - genetics
Chromosomes, Human, Pair 22 - genetics
Cognitive ability
development
Disease Models, Animal
External stimuli
Female
Gating
Gene deletion
Long QT Syndrome - genetics
Male
Mice
Mice, Inbred C57BL
mouse genetic models
Mutation
Nerve Tissue Proteins - genetics
Nerve Tissue Proteins - metabolism
Phelan‐McDermid syndrome
phenotyping
replication
Sensory evaluation
Shank3
Social Behavior
Social interactions
Syndactyly - genetics
Therapeutic applications
Timothy syndrome
title Comprehensive analysis of two Shank3 and the Cacna1c mouse models of autism spectrum disorder
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