Myb轉(zhuǎn)錄因子.ppt

Myb轉(zhuǎn)錄因子.ppt

ID:48428091

大?。?.54 MB

頁數(shù):20頁

時間:2020-01-19

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1、MybTranscriptionFactorLiuPeiyuMYBtranscriptionfactorsinplantsMorethan20yearsago,thefirstgeneencodingatranscriptionfactorinplantswasidentified——COLORED1(C1)Adecadeago,theArabidopsisgenomesequencewaspublished,whichprovidedthefirstcomprehensivedescriptionandc

2、lassificationofplantMYBgenes.Inrencentyears,thefunctionsofMYBproteinshavebeeninvestigatedinnumerousplantspecies.StructureandevolutionMYBproteinsarecharacterizedbyahighlyconservedDNA-bindingdomain:theMYBdomain(consistsofuptofourimperfectaminoacidsequencerep

3、eats(R)ofabout52aminoacids,eachformingthreea–helices).MYBproteinscanbedividedintodifferentclassesdependingonthenumberofadjacentrepeats(one,two,threeorfour)IncontrasttothehighlyconservedMYBdomain,theotherregionsofR2R3-MYBproteinsarehighlyvariable.Basedonthe

4、conservationoftheDNAbindingdomainandofaminoacidmotifsintheCterminaldomains,R2R3-MYBproteinshavebeendividedintosubgroups.DiversityoffunctionsNumerousR2R3-MYBproteinshavebeencharacterizedbygeneticapproachesandfoundtobeinvolvedinthecontrolofplant-specificproc

5、essesincluding:(i)primaryandsecondarymetabolism(ii)cellfateandidentity(iii)developmentalprocesses(iv)responsestobioticandabioticstressesRegulationofMYBfunctionsMYBgenesaretargetstobothmicroRNAs(miRNAs)andtransacting,silencingRNAs(ta-siRNAs).Post-translatio

6、nalmodificationsandprotein–proteininteractionscansignificantlyimpacttheregulatoryactivityofMYBtranscriptionfactors.ThetranscriptionalactivityofsomeR2R3-MYBfactorsisdependentinvivoonprotein–proteininteractions.PhosphorylationisimportantindeterminingMYBprote

7、inactivity.RedoxcontrolisthoughttoinfluenceMYBproteinactivitybecauseofthepresenceofapairofconservedCysresidues,fourresiduesapart,intheR2-MYBmotifofmost3R-andR2R3-MYBproteinsTheactivityofmanytranscriptionalregulatorsismodulatedbyconjugationwithubiquitinorth

8、esmallubiquitinrelatedmodifierThemodulationoftranscriptionfactoractivitybysumoylationcanoccurbymultiplemechanismsincludingsubcellularlocalization,DNA-bindingactivityordecreasingtheactivityofaTAD,asdescribedfo

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