Integrated Analysis of the Plasmodium Species Transcriptome (doi:10.21979/N9/UBCFAP)

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Part 1: Document Description
Part 2: Study Description
Part 3: Data Files Description
Part 4: Variable Description
Part 5: Other Study-Related Materials
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Document Description

Citation

Title:

Integrated Analysis of the Plasmodium Species Transcriptome

Identification Number:

doi:10.21979/N9/UBCFAP

Distributor:

DR-NTU (Data)

Date of Distribution:

2019-07-08

Version:

1

Bibliographic Citation:

Hoo, Regina May Ling, 2019, "Integrated Analysis of the Plasmodium Species Transcriptome", https://doi.org/10.21979/N9/UBCFAP, DR-NTU (Data), V1, UNF:6:1IVTRLN2QZa2dxWQtdfWVw== [fileUNF]

Study Description

Citation

Title:

Integrated Analysis of the Plasmodium Species Transcriptome

Identification Number:

doi:10.21979/N9/UBCFAP

Authoring Entity:

Hoo, Regina May Ling (Nanyang Technological University)

Software used in Production:

R

Grant Number:

NMRC/1292/2011

Grant Number:

1R01AI24710

Grant Number:

R01-AI065961

Grant Number:

ORIP/OD P51OD011132

Distributor:

DR-NTU (Data)

Access Authority:

Hoo, Regina May Ling

Depositor:

Hoo, Regina May Ling

Date of Deposit:

2019-07-05

Holdings Information:

https://doi.org/10.21979/N9/UBCFAP

Study Scope

Keywords:

Medicine, Health and Life Sciences, Medicine, Health and Life Sciences, malaria, transcriptome

Abstract:

The genome sequence available for different Plasmodium species is a valuable resource for understanding malaria parasite biology. However, comparative genomics on its own cannot fully explain all the species-specific differences which suggests that other genomic aspects such as regulation of gene expression play an important role in defining species-specific characteristics. Here, we developed a comprehensive approach to measure transcriptional changes of the evolutionary conserved syntenic orthologs during the intraerythrocytic developmental cycle across six Plasmodium species. We show significant transcriptional constraint at the mid-developmental stage of Plasmodium species while the earliest stages of parasite development display the greatest transcriptional variation associated with critical functional processes. Modeling of the evolutionary relationship based on changes in transcriptional profile reveal a phylogeny pattern of the Plasmodium species that strictly follows its mammalian hosts. In addition, the work shows that transcriptional conserved orthologs represent potential future targets for anti-malaria intervention as they would be expected to carry out key essential functions within the parasites. This work provides an integrated analysis of orthologs transcriptome, which aims to provide insights into the Plasmodium evolution thereby establishing a framework to explore complex pathways and drug discovery in Plasmodium species with broad host range.

Kind of Data:

Microarray data

Methodology and Processing

Sources Statement

Data Access

Other Study Description Materials

Related Publications

Citation

Identification Number:

10.1016/j.ebiom.2016.04.011

Bibliographic Citation:

Hoo, R., Zhu, L., Amaladoss, A., Mok, S., Natalang, O., Lapp, S. A., . . . Preiser, P. R. (2016). Integrated analysis of the Plasmodium species transcriptome. EBioMedicine, 7(1), 255-266.

Citation

Identification Number:

10356/89991

Bibliographic Citation:

Hoo, R., Zhu, L., Amaladoss, A., Mok, S., Natalang, O., Lapp, S. A., . . . Preiser, P. R. (2016). Integrated analysis of the Plasmodium species transcriptome. EBioMedicine, 7(1), 255-266.

File Description--f12784

File: Table S1.tab

  • Number of cases: 4754

  • No. of variables per record: 25

  • Type of File: text/tab-separated-values

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File Description--f12786

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  • No. of variables per record: 10

  • Type of File: text/tab-separated-values

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File Description--f12783

File: Table S4.tab

  • Number of cases: 241

  • No. of variables per record: 7

  • Type of File: text/tab-separated-values

Notes:

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Variable Description

List of Variables:

Variables

SupplementaryTable1:ProcessedmicroarrayhybridizationdataofP.falciparum(24time-points),P.knowlesi(7time-points),P.vivax(9time-points),P.yoelii(12time-points),P.berghei(12time-points)andP.chabaudi(12time-points)IDCtranscriptome

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SupplementaryTable3:Functionalenrichmentanalysisforoutlierspeciesorthologsusinghypergeometricdistributionfunction,relatedtoFigure4b.

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SupplementaryTable4:Listof240transcriptionallyconservedorthologswithpositivedruggabilityindexscore(DIS)obtainedfromTDRdatabase,withitscorrespondingpeakexpressioninIDC,relatedtoFigure6.YdenotesessentialityevidenceinP.bergheiknockoutstudiesfromRMgmDB.

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