dtorsin, the Drosophila Ortholog of the Early-Onset Dystonia TOR1A (DYT1), Plays a Novel Role in Dopamine Metabolism 英文参考文献.docVIP

下载本文档

5
0
约6.9万字
约 15页
2017-05-11 发布于上海
举报
版权申诉

dtorsin, the Drosophila Ortholog of the Early-Onset Dystonia TOR1A (DYT1), Plays a Novel Role in Dopamine Metabolism 英文参考文献.doc

1、本文档共15页，可阅读全部内容。
2、原创力文档（book118）网站文档一经付费（服务费），不意味着购买了该文档的版权，仅供个人/单位学习、研究之用，不得用于商业用途，未经授权，严禁复制、发行、汇编、翻译或者网络传播等，侵权必究。
3、本站所有内容均由合作方或网友上传，本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺！文档内容仅供研究参考，付费前请自行鉴别。如您付费，意味着您自己接受本站规则且自行承担风险，本站不退款、不进行额外附加服务；查看《如何避免下载的几个坑》。如果您已付费下载过本站文档，您可以点击这里二次下载。
4、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等，请点击“版权申诉”（推荐），也可以打举报电话：400-050-0827(电话支持时间：9:00-18:30)。
5、该文档为VIP文档，如果想要下载，成为VIP会员后，下载免费。
6、成为VIP后，下载本文档将扣除1次下载权益。下载后，不支持退款、换文档。如有疑问请联系我们。
7、成为VIP后，您将拥有八大权益，权益包括：VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
8、VIP文档为合作方或网友上传，每下载1次，网站将根据用户上传文档的质量评分、类型等，对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档

dtorsin, the Drosophila Ortholog of the Early-Onset Dystonia TOR1A (DYT1), Plays a Novel Role in Dopamine Metabolism 英文参考文献

dtorsin,theDrosophilaOrthologoftheEarly-Onset DystoniaTOR1A(DYT1),PlaysaNovelRoleinDopamine Metabolism NorikoWakabayashi-Ito1,4,OlugbengaM.Doherty2,HideakiMoriyama3,XandraO.Breakefield4, JamesF.Gusella1,JanisM.O’Donnell2,NaotoIto1,4* 1CenterforHumanGeneticResearch,MassachusettsGeneralHospital,Boston,Massachusetts,UnitedStatesofAmerica,2DepartmentofBiologicalSciences,University ofAlabama,Tuscaloosa,Alabama,UnitedStatesofAmerica,3SchoolofBiologicalScience,UniversityofNebraska-Lincoln,Lincoln,Nebraska,UnitedStatesofAmerica, 4DepartmentofNeurologyandRadiology,MassachusettsGeneralHospitalandPrograminNeuroscience,HarvardMedicalSchool,Boston,Massachusetts,UnitedStates ofAmerica Abstract Dystoniarepresentsthethirdmostcommonmovementdisorderinhumans.Atleast15geneticloci(DYT1-15)havebeen identifiedandsomeofthesegeneshavebeencloned.TOR1A(formallyDYT1),thegeneresponsibleforthemostcommon primaryhereditarydystonia,encodestorsinA,anAAAATPasefamilyprotein.However,thefunctionoftorsinAhasyettobe fully understood. Here, we have generated and characterized a complete loss-of-function mutant for dtorsin, the only DrosophilaorthologofTOR1A.NullmutationoftheX-linkeddtorsinwassemi-lethalwithmostmalefliesdyingbythepre- pupalstageandthefewsurvivingadultsbeingsterileandslowmoving,withreducedcuticlepigmentationandthin,short bristles. Third instar male larvae exhibited locomotion defects that were rescued by feeding dopamine. Moreover, biochemicalanalysisrevealedthatthebrainsofthirdinstarlarvaeandadultsheterozygousfortheloss-of-functiondtorsin mutationhadsignificantlyreduceddopaminelevels.ThedtorsinmutantshowedaverystronggeneticinteractionwithPu (Punch:GTPcyclohydrolase),theorthologofthehumangeneunderlyingDYT14dystonia.Biochemicalanalysesrevealeda severe reduction of GTP cyclohydrolase protein and activity, suggesting that dtorsin plays a novel role in dopamine metabolism as a positive-regulator of GTP cyclohydrolase protein. This dtorsin mutant line will be valuable for understandingthisrela