简介:TheaimofthisstudyistoexplorethegenomicmolecularorganizationandgenogroupofhumannorovirusfrominfectedinfantsinGuangzhouofChina.PrimersweredesignedaccordingtothegenomicsequenceofnorovirusintheGenBank,andthenorovirusgenomewasamplifiedbyRT-PCR.ThePCR-productswereclonedintoTvectorandsequenced,andthegenomicnucleotidesequenceswereanalyzedwiththeprogramsCLUSTALW/X,DNASTARandRAT(RecombinationAnalysisTool).TheNVgz01straingenomeis7558bpinlengthandencodesthreeopenreadingframes(GenBankaccessionNo.isDQ369797).ThegenomicsequencesofNVgz01werecomparedwiththoseofnomvirusinGenBank,whichrevealedthatthehomologywithgenogroupⅡrangesbetween76%-90%,andgenogroupⅠbe-tween43%-44%.TheORF1regionshared94%and88%identitywithMc37andFarmingtonstrains,respectively;thecapsidregion(ORF2)shared65%and94%identitywithMc37andFarmingtonstrains,respectively.Phylogenetictreeswerereconstructedbytheneighbor-joiningmethod.ComparativecompletesequenceanalysisoftheNVgz01withreportedhumannorovimsgenomicsequencesrevealedthatthisisolatebelongstogenogmupⅡ.TheORF1andORF2regionsshareddifferentidentitywithMc37andFarmingtonstrains,suggestingNVgz01couldbearecombinantvires.
简介:Noise-inducedHearingLossandNeuroplasticityThe6th《ChineseJoumedofOtology》andthe5thJournalofOtologyEditorialBoard11thSeniorSeminarofotomicrosurgery&otoneurosurgeryThefourthadvancedseminarofinternationalaudiologicalmedicineThe6thInternationalSymposiumofDeafnessandGeneticMedicineandThe8thNationalClassesofDeafnessandGeneticDiagnosis
简介:摘要在法医医学鉴定过程中经常会遇到基因丢失的情况,导致亲子代在基因鉴定过程中出现不符合遗传规律的情况,在一定程度上增加了被错误排除的风险。由于等位基因的缺失在一定程度上和模板的DNA多态性、碱基的插入或缺失有关,因此正确识别和分析等位基因对鉴定结果会产生直接的影响。基于此,本文作者结合自身实践就TH01基因座丢失的相关问题进行相关阐述。