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dc.contributor.authorMair, GR
dc.contributor.authorLasonder, Edwin
dc.contributor.authorGarver, LS
dc.contributor.authorFranke-Fayard, BMD
dc.contributor.authorCarret, CK
dc.contributor.authorWiegant, JCAG
dc.contributor.authorDirks, RW
dc.contributor.authorDimopoulos, G
dc.contributor.authorJanse, CJ
dc.contributor.authorWaters, AP
dc.date.accessioned2016-07-11T15:04:41Z
dc.date.available2016-07-11T15:04:41Z
dc.date.issued2010-02
dc.identifier.issn1553-7366
dc.identifier.issn1553-7374
dc.identifier.otherARTN e1000767
dc.identifier.urihttp://hdl.handle.net/10026.1/5044
dc.description.abstract

A universal feature of metazoan sexual development is the generation of oocyte P granules that withhold certain mRNA species from translation to provide coding potential for proteins during early post-fertilization development. Stabilisation of translationally quiescent mRNA pools in female Plasmodium gametocytes depends on the RNA helicase DOZI, but the molecular machinery involved in the silencing of transcripts in these protozoans is unknown. Using affinity purification coupled with mass-spectrometric analysis we identify a messenger ribonucleoprotein (mRNP) from Plasmodium berghei gametocytes defined by DOZI and the Sm-like factor CITH (homolog of worm CAR-I and fly Trailer Hitch). This mRNP includes 16 major factors, including proteins with homologies to components of metazoan P granules and archaeal proteins. Containing translationally silent transcripts, this mRNP integrates eIF4E and poly(A)-binding protein but excludes P body RNA degradation factors and translation-initiation promoting eIF4G. Gene deletion mutants of 2 core components of this mRNP (DOZI and CITH) are fertilization-competent, but zygotes fail to develop into ookinetes in a female gametocyte-mutant fashion. Through RNA-immunoprecipitation and global expression profiling of CITH-KO mutants we highlight CITH as a crucial repressor of maternally supplied mRNAs. Our data define Plasmodium P granules as an ancient mRNP whose protein core has remained evolutionarily conserved from single-cell organisms to germ cells of multi-cellular animals and stores translationally silent mRNAs that are critical for early post-fertilization development during the initial stages of mosquito infection. Therefore, translational repression may offer avenues as a target for the generation of transmission blocking strategies and contribute to limiting the spread of malaria.

dc.format.extente1000767-e1000767
dc.format.mediumElectronic
dc.languageen
dc.language.isoeng
dc.publisherPublic Library of Science (PLoS)
dc.subjectAnimals
dc.subjectBlotting, Southern
dc.subjectBlotting, Western
dc.subjectFemale
dc.subjectFlow Cytometry
dc.subjectGene Expression
dc.subjectGene Expression Profiling
dc.subjectGene Expression Regulation
dc.subjectGerm Cells
dc.subjectImmunoprecipitation
dc.subjectPhylogeny
dc.subjectPlasmodium berghei
dc.subjectProtozoan Proteins
dc.subjectRNA Interference
dc.subjectRNA, Messenger
dc.subjectRibonucleoproteins
dc.subjectSexual Development
dc.subjectZygote
dc.titleUniversal Features of Post-Transcriptional Gene Regulation Are Critical for Plasmodium Zygote Development
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, N.I.H., Extramural
dc.typeResearch Support, Non-U.S. Gov't
dc.typeResearch Support, U.S. Gov't, Non-P.H.S.
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000275295900019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue2
plymouth.volume6
plymouth.publication-statusPublished online
plymouth.journalPLoS Pathogens
dc.identifier.doi10.1371/journal.ppat.1000767
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
dc.publisher.placeUnited States
dcterms.dateAccepted2010-01-13
dc.identifier.eissn1553-7374
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.1371/journal.ppat.1000767
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2010-02-12
rioxxterms.typeJournal Article/Review


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