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Series GSE166390 Query DataSets for GSE166390
Status Public on Jul 01, 2021
Title Expression patterns of Plasmodium falciparum clonally variant genes at the onset of a blood infection in non-immune humans [ChIP-seq]
Organism Plasmodium falciparum
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Clonally variant genes (CVGs) play fundamental roles in the adaptation of Plasmodium falciparum parasites to the fluctuating conditions of the human host, but their expression patterns under the natural conditions of the blood circulation have been characterized in detail only for a few specific gene families. Here we provide a detailed characterization of the full P. falciparum transcriptome across the full intraerythrocytic development cycle (IDC) at the onset of a blood infection in non-immune human volunteers. We found that the vast majority of transcriptional differences between parasites obtained from the volunteers and the parental parasite line maintained in culture occur for CVGs. Specifically, we observed a major increase in the transcript levels of most members of the pfmc-2tm and gbp families and of specific genes of other families, in addition to previously reported changes in var and clag3 genes. The expression patterns were almost identical between parasites obtained from the different volunteers. Large transcriptional differences correlate with changes in the distribution of histone modifications associated with heterochromatin, confirming their epigenetic nature. The analysis of parasites collected at different points along the infection indicates that when parasites pass through transmission stages, the epigenetic memory at CVG loci is lost, resulting in a reset of their expression state and reestablishment of new epigenetic patterns.
 
Overall design Samples from the NF54 parental line and V63 (parasites obtained from a volunteer who participated in a controlled human malaria infection trial) were processed to perform a ChIP-Seq experiment against H3K9me3.
 
Contributor(s) Pickford A, Michel-Todó L, Cortés A
Citation(s) 34340541
Submission date Feb 08, 2021
Last update date Sep 14, 2021
Contact name Anastasia Pickford
E-mail(s) anastasia.pickford@isglobal.org
Organization name ISGlobal
Lab Malaria Epigenetics
Street address Carrer Rosselló 153
City Barcelona
State/province Barcelona
ZIP/Postal code 08036
Country Spain
 
Platforms (1)
GPL21078 Illumina HiSeq 2500 (Plasmodium falciparum)
Samples (4)
GSM5070347 H3K9me3 ChIP-Seq NF54
GSM5070348 Input of NF54
GSM5070349 H3K9me3 ChIP-Seq V63
Relations
BioProject PRJNA700660
SRA SRP305362

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE166390_NF54IP_Macspeaks_peaks.narrowPeak.gz 6.8 Kb (ftp)(http) NARROWPEAK
GSE166390_NF54IP_vs_V63IP_g250_l300_c5_c5.0_cond1.bed.gz 3.4 Kb (ftp)(http) BED
GSE166390_NF54IP_vs_V63IP_g250_l300_c5_c5.0_cond2.bed.gz 3.1 Kb (ftp)(http) BED
GSE166390_V63IP_Macspeaks_peaks.narrowPeak.gz 7.9 Kb (ftp)(http) NARROWPEAK
GSE166390_coverage_NF54_genewise.bed.gz 144.5 Kb (ftp)(http) BED
GSE166390_coverage_V63_genewise.bed.gz 146.2 Kb (ftp)(http) BED
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Raw data are available in SRA
Processed data are available on Series record

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