Evidence map›Paper›PMID 25759501›Full record

ArticlemBio2015

Regulation of Plasmodium yoelii oocyst development by strain- and stage-specific small-subunit rRNA.

Yanwei Qi, Feng Zhu, Richard T Eastman, Young Fu, Martine Zilversmit, Sittiporn Pattaradilokrat, Lingxian Hong, Shengfa Liu, Thomas F McCutchan, Weiqing Pan and 4 more

Open access · goldAbstract read
In one paragraph

Article in mBio, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Impacts of ribosomal RNA sequence variation on gene expression and phenotype.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2025
    Review
  4. Article
  5. Ribosome Specialization in Protozoa Parasites.International journal of molecular sciences · 2023
    Review
  6. Article
  7. Review
  8. RNA Secondary Structurome Revealed Distinct Thermoregulation inFrontiers in cell and developmental biology · 2021
    Article
  9. Frontiers in cellular and infection microbiology · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
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

14 authors at 6 institutions in 3 countries.

Yanwei Qi
Feng Zhu
Richard T EastmanLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, Maryland, USA.
Young FuDepartment of Pathogenic Biology, The Third Military Medical University, Chongqing, People's Republic of China.
Martine ZilversmitLaboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Bethesda, Maryland, USA.
Sittiporn Pattaradilokrat
Lingxian HongState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian, People's Republic of China.
Shengfa LiuState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian, People's Republic of China.
Thomas F McCutchanDepartment of Pathogen Biology, The Second Military Medical University, Shanghai, China.
Weiqing PanDepartment of Pathogen Biology, The Second Military Medical University, Shanghai, China.
Wenyue XuDepartment of Pathogenic Biology, The Third Military Medical University, Chongqing, People's Republic of China.
Jian LiState Key Laboratory of Cellular Stress Biology, Innovation Center for Cell Signaling Network, School of Life Sciences, Xiamen University, Xiamen, Fujian, People's Republic of China fushenghster@gmail.com jianli_204@xmu.edu.cn xsu@niaid.nih.gov.
Fusheng HuangDepartment of Pathogenic Biology, The Third Military Medical University, Chongqing, People's Republic of China fushenghster@gmail.com jianli_204@xmu.edu.cn xsu@niaid.nih.gov.
Xin-zhuan Sufushenghster@gmail.com jianli_204@xmu.edu.cn xsu@niaid.nih.gov.
Xiamen University · CNArmy Medical University · CNNational Institutes of Health · USSecond Military Medical University · CNChulalongkorn University · THNational Institute of Allergy and Infectious Diseases · US

Funding

Malaria Parasite Sexual Development, Drug Resistance, and EvolutionZIAAI000892 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI SU, XINZHUAN · 2009 to 2025
$23.3M
Intramural NIH HHS
6 · The paper itself

Abstract

unlabelledOne unique feature of malaria parasites is the differential transcription of structurally distinct rRNA (rRNA) genes at different developmental stages: the A-type genes are transcribed mainly in asexual stages, whereas the S-type genes are expressed mostly in sexual or mosquito stages. Conclusive functional evidence of different rRNAs in regulating stage-specific parasite development, however, is still absent. Here we performed genetic crosses of Plasmodium yoelii parasites with one parent having an oocyst development defect (ODD) phenotype and another producing normal oocysts to identify the gene(s) contributing to the ODD. The parent with ODD--characterized as having small oocysts and lacking infective sporozoites--was obtained after introduction of a plasmid with a green fluorescent protein gene into the parasite genome and subsequent passages in mice. Quantitative trait locus analysis of genome-wide microsatellite genotypes of 48 progeny from the crosses linked an ~200-kb segment on chromosome 6 containing one of the S-type genes (D-type small subunit rRNA gene [D-ssu]) to the ODD. Fine mapping of the plasmid integration site, gene expression pattern, and gene knockout experiments demonstrated that disruption of the D-ssu gene caused the ODD phenotype. Interestingly, introduction of the D-ssu gene into the same parasite strain (self), but not into a different subspecies, significantly affected or completely ablated oocyst development, suggesting a stage- and subspecies (strain)-specific regulation of oocyst development by D-ssu. This study demonstrates that P. yoelii D-ssu is essential for normal oocyst and sporozoite development and that variation in the D-ssu sequence can have dramatic effects on parasite development. IMPORTANCE: Malaria parasites are the only known organisms that express structurally distinct rRNA genes at different developmental stages. The differential expression of these genes suggests that they play unique roles during the complex life cycle of the parasites. Conclusive functional proof of different rRNAs in regulating parasite development, however, is still absent or controversial. Here we functionally demonstrate for the first time that a stage-specifically expressed D-type small-subunit rRNA gene (D-ssu) is essential for oocyst development of the malaria parasite Plasmodium yoelii in the mosquito. This study also shows that variations in D-ssu sequence and/or the timing of transcription may have profound effects on parasite oocyst development. The results show that in addition to protein translation, rRNAs of malaria parasites also regulate parasite development and differentiation in a strain-specific manner, which can be explored for controlling parasite transmission.

Indexed as

Gene Expression Regulation, DevelopmentalAnimalsChromosome MappingCrosses, GeneticGene Knockout TechniquesMiceMicrosatellite RepeatsOocystsPlasmodium yoeliiQuantitative Trait LociRecombination, GeneticRNA, Ribosomal, 18SRNA, Ribosomal, 18S

Identifiers

PMID25759501
PMCPMC4453563
OpenAlexW2163915500

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.