Katarina Micovic, Alicia Canuel, Aasiya Remtulla, Alexandre Chuyen, Margarita Byrsan, David J. McGarry, Michael F. Olson
{"title":"在表达酪氨酸酶的细胞中删除 Mical1 会影响小鼠的奔跑步态。","authors":"Katarina Micovic, Alicia Canuel, Aasiya Remtulla, Alexandre Chuyen, Margarita Byrsan, David J. McGarry, Michael F. Olson","doi":"10.1111/gbb.70004","DOIUrl":null,"url":null,"abstract":"<p>Neuronal development is a highly regulated process that is dependent on the correct coordination of cellular responses to extracellular cues. In response to semaphorin axon guidance proteins, the MICAL1 protein is stimulated to produce reactive oxygen species that oxidize actin on specific methionine residues, leading to filamentous actin depolymerization and consequent changes in neuronal growth cone dynamics. Crossing genetically modified mice homozygous for floxed <i>Mical1</i> (<i>Mical1</i><sup><i>fl/fl</i></sup>) alleles with transgenic mice expressing Cre recombinase under the control of a <i>tyrosinase</i> gene enhancer/promoter (<i>Tyr::Cre</i>) enabled conditional <i>Mical1</i> deletion. Immunohistochemical analysis showed <i>Mical1</i> expression in the cerebellum, which plays a prominent role in the coordination of motor movements, with reduced <i>Mical1</i> expression in <i>Mical1</i><sup><i>fl/fl</i></sup> mice co-expressing <i>Tyr::Cre</i>. Analysis of the gaits of mice running on a treadmill showed that both male and female <i>Mical1</i><sup><i>fl/fl</i></sup>, <i>Tyr::Cre</i> mutant mice had significant alterations to their striding patterns relative to wild-type mice, although the specific aspects of their altered gaits differed between the sexes. Additional motor tests that involved movement on a rotating rod, descending a vertical pole, or crossing a balance beam did not show significant differences between the genotypes, suggesting that the effect of the <i>Mical1</i><sup><i>fl/fl</i></sup>, <i>Tyr::Cre</i> genetic modifications was only manifested during specific highly coordinated movements that contribute to running. These findings indicate that there is a behavioral consequence in <i>Mical1</i><sup><i>fl/fl</i></sup>, <i>Tyr::Cre</i> mutant mice that affects motor control as manifested by alterations in their gait.</p>","PeriodicalId":50426,"journal":{"name":"Genes Brain and Behavior","volume":"23 5","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2024-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbb.70004","citationCount":"0","resultStr":"{\"title\":\"Mical1 deletion in tyrosinase expressing cells affects mouse running gaits\",\"authors\":\"Katarina Micovic, Alicia Canuel, Aasiya Remtulla, Alexandre Chuyen, Margarita Byrsan, David J. McGarry, Michael F. Olson\",\"doi\":\"10.1111/gbb.70004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Neuronal development is a highly regulated process that is dependent on the correct coordination of cellular responses to extracellular cues. In response to semaphorin axon guidance proteins, the MICAL1 protein is stimulated to produce reactive oxygen species that oxidize actin on specific methionine residues, leading to filamentous actin depolymerization and consequent changes in neuronal growth cone dynamics. Crossing genetically modified mice homozygous for floxed <i>Mical1</i> (<i>Mical1</i><sup><i>fl/fl</i></sup>) alleles with transgenic mice expressing Cre recombinase under the control of a <i>tyrosinase</i> gene enhancer/promoter (<i>Tyr::Cre</i>) enabled conditional <i>Mical1</i> deletion. Immunohistochemical analysis showed <i>Mical1</i> expression in the cerebellum, which plays a prominent role in the coordination of motor movements, with reduced <i>Mical1</i> expression in <i>Mical1</i><sup><i>fl/fl</i></sup> mice co-expressing <i>Tyr::Cre</i>. Analysis of the gaits of mice running on a treadmill showed that both male and female <i>Mical1</i><sup><i>fl/fl</i></sup>, <i>Tyr::Cre</i> mutant mice had significant alterations to their striding patterns relative to wild-type mice, although the specific aspects of their altered gaits differed between the sexes. Additional motor tests that involved movement on a rotating rod, descending a vertical pole, or crossing a balance beam did not show significant differences between the genotypes, suggesting that the effect of the <i>Mical1</i><sup><i>fl/fl</i></sup>, <i>Tyr::Cre</i> genetic modifications was only manifested during specific highly coordinated movements that contribute to running. These findings indicate that there is a behavioral consequence in <i>Mical1</i><sup><i>fl/fl</i></sup>, <i>Tyr::Cre</i> mutant mice that affects motor control as manifested by alterations in their gait.</p>\",\"PeriodicalId\":50426,\"journal\":{\"name\":\"Genes Brain and Behavior\",\"volume\":\"23 5\",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-09-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/gbb.70004\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Genes Brain and Behavior\",\"FirstCategoryId\":\"102\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/gbb.70004\",\"RegionNum\":4,\"RegionCategory\":\"心理学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Genes Brain and Behavior","FirstCategoryId":"102","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/gbb.70004","RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
Mical1 deletion in tyrosinase expressing cells affects mouse running gaits
Neuronal development is a highly regulated process that is dependent on the correct coordination of cellular responses to extracellular cues. In response to semaphorin axon guidance proteins, the MICAL1 protein is stimulated to produce reactive oxygen species that oxidize actin on specific methionine residues, leading to filamentous actin depolymerization and consequent changes in neuronal growth cone dynamics. Crossing genetically modified mice homozygous for floxed Mical1 (Mical1fl/fl) alleles with transgenic mice expressing Cre recombinase under the control of a tyrosinase gene enhancer/promoter (Tyr::Cre) enabled conditional Mical1 deletion. Immunohistochemical analysis showed Mical1 expression in the cerebellum, which plays a prominent role in the coordination of motor movements, with reduced Mical1 expression in Mical1fl/fl mice co-expressing Tyr::Cre. Analysis of the gaits of mice running on a treadmill showed that both male and female Mical1fl/fl, Tyr::Cre mutant mice had significant alterations to their striding patterns relative to wild-type mice, although the specific aspects of their altered gaits differed between the sexes. Additional motor tests that involved movement on a rotating rod, descending a vertical pole, or crossing a balance beam did not show significant differences between the genotypes, suggesting that the effect of the Mical1fl/fl, Tyr::Cre genetic modifications was only manifested during specific highly coordinated movements that contribute to running. These findings indicate that there is a behavioral consequence in Mical1fl/fl, Tyr::Cre mutant mice that affects motor control as manifested by alterations in their gait.
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