Evidence map›Paper›PMID 30703164›Full record

ArticlePLoS pathogens2019

Plasmodium male gametocyte development and transmission are critically regulated by the two putative deadenylases of the CAF1/CCR4/NOT complex.

Kevin J Hart, Jenna Oberstaller, Michael P Walker, Allen M Minns, Mark F Kennedy, Ian Padykula, John H Adams, Scott E Lindner

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 55 citations in OpenAlex.

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  8. Global Release of Translational Repression AcrossbioRxiv : the preprint server for biology · 2024
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  13. Identification of basal complex protein that is essential for maturation of transmission-stage malaria parasites.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
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  15. Adapt or Die: Targeting Unique Transmission-Stage Biology for Malaria Elimination.Frontiers in cellular and infection microbiology · 2022
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Kevin J HartDepartment of Biochemistry and Molecular Biology, Center for Malaria Research, Pennsylvania State University, University Park, State College, Pennsylvania, United States of America.ORCID 0000-0001-8250-7822
Jenna OberstallerCenter for Global Health and Infectious Diseases Research, Department of Global Health, University of South Florida, Tampa, Florida, United States of America.ORCID 0000-0002-3033-2212
Michael P WalkerDepartment of Biochemistry and Molecular Biology, Center for Malaria Research, Pennsylvania State University, University Park, State College, Pennsylvania, United States of America.
Allen M MinnsDepartment of Biochemistry and Molecular Biology, Center for Malaria Research, Pennsylvania State University, University Park, State College, Pennsylvania, United States of America.
Mark F KennedyDepartment of Biochemistry and Molecular Biology, Center for Malaria Research, Pennsylvania State University, University Park, State College, Pennsylvania, United States of America.
Ian PadykulaCenter for Global Health and Infectious Diseases Research, Department of Global Health, University of South Florida, Tampa, Florida, United States of America.ORCID 0000-0003-2889-1864
John H AdamsCenter for Global Health and Infectious Diseases Research, Department of Global Health, University of South Florida, Tampa, Florida, United States of America.ORCID 0000-0003-3707-7979
Scott E LindnerDepartment of Biochemistry and Molecular Biology, Center for Malaria Research, Pennsylvania State University, University Park, State College, Pennsylvania, United States of America.ORCID 0000-0003-1799-3726
Pennsylvania State University · USUniversity of South Florida · US

Funding

Discovering the essential genome of Plasmodium falciparumR01AI130171 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI ADAMS, JOHN H · 2018 to 2021
$2.8M
Mechanisms Governing Translational Regulation During Plasmodium TransmissionR01AI123341 · NIAID · PENNSYLVANIA STATE UNIVERSITY, THE · PI LINDNER, SCOTT E · 2017 to 2021
$1.9M
A large-scale transposon mutagenesis screen of Plasmodium falciparumR01AI094973 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI ADAMS, JOHN H · 2011 to 2015
$1.8M
Dissection of RNA Storage Granules Essential to Plasmodium TransmissionK22AI101039 · NIAID · PENNSYLVANIA STATE UNIVERSITY, THE · PI LINDNER, SCOTT E · 2013 to 2014
$250k
Post-transcriptional regulation in the malaria parasite blood stageF32AI112271 · NIAID · UNIVERSITY OF SOUTH FLORIDA · PI OBERSTALLER, JENNA · 2015 to 2017
$173k
MUTATION RATES OF DRUG RESISTANT HIV1 VARIANTSF32AI010139 · NIAID · UNIVERSITY OF UTAH · PI SMITH, ROBERT A · 1998 to 2000
$38k
NIAID NIH HHS F32 AI010139NIAID NIH HHS F32 AI112271NIAID NIH HHS K22 AI101039NIAID NIH HHS R01 AI094973NIAID NIH HHS R01 AI123341NIAID NIH HHS R01 AI130171
6 · The paper itself

Abstract

With relatively few known specific transcription factors to control the abundance of specific mRNAs, Plasmodium parasites may rely more on the regulation of transcript stability and turnover to provide sufficient gene regulation. Plasmodium transmission stages impose translational repression on specific transcripts in part to accomplish this. However, few proteins are known to participate in this process, and those that are characterized primarily affect female gametocytes. We have identified and characterized Plasmodium yoelii (Py) CCR4-1, a putative deadenylase, which plays a role in the development and activation of male gametocytes, regulates the abundance of specific mRNAs in gametocytes, and ultimately increases the efficiency of host-to-vector transmission. We find that when pyccr4-1 is deleted or its protein made catalytically inactive, there is a loss in the initial coordination of male gametocyte maturation and a reduction of parasite infectivity of the mosquito. Expression of only the N-terminal CAF1 domain of the essential CAF1 deadenylase leads to a similar phenotype. Comparative RNA-seq revealed that PyCCR4-1 affects transcripts important for transmission-related functions that are associated with male or female gametocytes, some of which directly associate with the immunoprecipitated complex. Finally, circular RT-PCR of one of the bound, dysregulated transcripts showed that deletion of the pyccr4-1 gene does not result in gross changes to its UTR or poly(A) tail length. We conclude that the two putative deadenylases of the CAF1/CCR4/NOT complex play critical and intertwined roles in gametocyte maturation and transmission.

Indexed as

AnimalsCulicidaeExoribonucleasesGametogenesisGene Expression RegulationHomeodomain ProteinsMaleMiceMosquito VectorsPlasmodiumPlasmodium falciparumProteinsReceptors, CCR4Repressor ProteinsRibonucleasesRNA, MessengerCcr4 protein, mouseCnot7 protein, mouseExoribonucleasesHomeodomain ProteinsNot protein, mouseProteinsReceptors, CCR4Repressor ProteinsRibonucleasesRNA, MessengerTranscription Factors

Identifiers

PMID30703164
PMCPMC6355032
OpenAlexW2914349013

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.