Translation reinitiation and development are compromised in similar ways by mutations in translation initiation factor eIF3h and the ribosomal protein RPL24 英文参考文献.docVIP
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Translation reinitiation and development are compromised in similar ways by mutations in translation initiation factor eIF3h and the ribosomal protein RPL24 英文参考文献
Zhouetal.BMCPlantBiology2010,10:193
/1471-2229/10/193
RESEARCH ARTICLE
OpenAccess
Translationreinitiationanddevelopmentare
compromisedinsimilarwaysbymutationsin
translationinitiationfactoreIF3handthe
ribosomalproteinRPL24
FujunZhou1,3,BijoyitaRoy2,AlbrechtGvonArnim2*
Abstract
Background:Withinthescanningmodeloftranslationinitiation,reinitiationisanon-canonicalmechanismthat
operatesonmRNAsharboringupstreamopenreadingframes.Thehsubunitofeukaryoticinitiationfactor3(eIF3)
booststranslationreinitiationontheuORF-containingmRNAcodingfortheArabidopsisbZiptranscriptionfactor,
AtbZip11,amongothers.TheRPL24Bproteinofthelargeribosomalsubunit,whichisencodedbySHORTVALVE1,
likewisefosterstranslationofuORF-containingmRNAs,forexamplemRNAsforauxinresponsetranscriptionfactors
(ARFs).
Results:HerewetestedthehypothesisthatRPL24BandeIF3haffecttranslationreinitiationinasimilarfashion.
First,likeeif3hmutants,rpl24bmutantsunder-translatetheAtbZip11mRNA,andthedetailedspectrumof
translationaldefectsinrpl24bisremarkablysimilartothatofeif3h.Second,eif3hmutantsdisplaydefectsinauxin
mediatedorganogenesisandgeneexpression,similartorpl24b.LikeAtbZip11,theuORF-containingARFmRNAs
areindeedundertranslatedineif3hmutantseedlings.
Conclusion:Weconcludethat,similartoeIF3h,RPL24BbolstersthereinitiationcompetenceofuORF-translating
ribosomes.CoordinationbetweeneIF3andthelargeribosomalsubunithelpstofine-tunetranslationofuORF-
containingmRNAsand,inturn,toorchestrateplantdevelopment.
Background
good as soon as it has terminated translation at a stop
Ineukaryotic cells, geneexpression ishighly regulated, codon. However, there are exceptions to this rule. In
often at multiple levels, such as transcription, mRNA Arabidopsis, about 30% of full-length mRNAs harbor
structureandstability,translationalcontrol,andprotein oneormoreupstreamopenreadingframes(uORFs)in
degradation. Translational regulation is arguably least their 5′ leader sequence [8]. Once a uORF has been
well characterized, and questions conce
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