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Series GSE57439 Query DataSets for GSE57439
Status Public on May 08, 2015
Title Deep, strand-specific, non-polyA-selected RNA sequencing of biological replicate Plasmodium falciparum blood stage time-courses
Organism Plasmodium falciparum
Experiment type Non-coding RNA profiling by high throughput sequencing
Summary The human malaria parasite Plasmodium falciparum has a complex and multi-stage life cycle that requires extensive immune escape, invasion of human liver and blood cells, and transmission through the female Anopholes mosquito. To date, the regulatory elements orchestrating these critical parasite processes remain largely unknown. However, there is mounting evidence across a broad range of species that intergenic long non-coding RNA (lncRNA) and antisense RNA can regulate chromatin state and gene expression. To pursue such functional roles for lncRNAs in P. falciparum, we performed deep, strand-specific RNA sequencing of fifteen non-polyA-selected blood stage samples, and assembled and characterized the properties of 660 intergenic lncRNAs, 474 antisense RNAs, and 1381 circular RNAs (circRNAs). We further validated the non-canonical splice junctions of seven P. falciparum circRNAs, an emerging class of non-coding RNA with regulatory potential and unexplored functional significance in P. falciparum. Our comprehensive analysis of P. falciparum lncRNAs indicates a functional role for these transcripts; P. falciparum intergenic lncRNAs and antisense RNAs are developmentally regulated in a similar periodic fashion to annotated transcripts, and sense-antisense pair expression is significantly anti-correlated. Notable outliers include intergenic lncRNAs that strongly peak in expression during parasite invasion, such as the telomere-associated lncRNA-TARE family, antisense transcripts that drop in expression during parasite invasion, and a highly correlated, multi-exonic, antisense counterpart to P. falciparum Gametocyte Developmental Protein 1 (PfGDV1). Taken together, our results present over two thousand P. falciparum intergenic lncRNA, antisense, and circRNA candidates and highlight promising P. falciparum lncRNAs for future investigation.
 
Overall design We harvested fifteen blood stage samples from two biological replicate time-courses. The first time-course comprised of eleven samples that finely map temporal changes during P. falciparum blood stage development. We harvested samples over 56 hours, at roughly 4-hour time intervals, from a tightly synchronized P. falciparum 3D7 parasite population. As the asexual blood stage is an approximately 48-hour cycle, this time-course allowed us to profile gene expression during RBC rupture and parasite invasion. The second time-course comprised of four samples harvested in synchronous P. falciparum 3D7 parasites approximately four hours before and after the ring to trophozoite and trophozoite to schizont morphological stage transitions, which occur during the blood stage at 24 hours post invasion (hpi) and 36 hpi, respectively.
 
Contributor(s) Broadbent K, Broadbent JC, Ribacke U, Wirth D, Rinn JL, Sabeti PC
Citation(s) 26070627
Submission date May 08, 2014
Last update date Jul 31, 2019
Contact name Kate Mariel Broadbent
E-mail(s) kbroadb@fas.harvard.edu
Organization name Harvard University
Department Systems Biology
Lab Pardis Sabeti
Street address FAS Center for Systems Biology Northwest Building, room 469 52 Oxford Street
City Cambridge
State/province MA
ZIP/Postal code 02138
Country USA
 
Platforms (1)
GPL16607 Illumina HiSeq 2000 (Plasmodium falciparum)
Samples (15)
GSM1382510 T6
GSM1382511 T14
GSM1382512 T20
Relations
BioProject PRJNA246463
SRA SRP041795

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Supplementary file Size Download File type/resource
GSE57439_LncRNA_Properties.xlsx.gz 437.0 Kb (ftp)(http) XLSX
GSE57439_PlasmoDBv10_Expression_FPKMs.txt.gz 360.5 Kb (ftp)(http) TXT
GSE57439_Significant_Features.xlsx.gz 398.9 Kb (ftp)(http) XLSX
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Processed data are available on Series record

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