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Links from GEO DataSets

Items: 20

1.

Histone variant, H2B.Z demarcates the AT-rich promoter regions of the Plasmodium falciparum genome

(Submitter supplied) Histone variants are key components of the epigenetic code and evolved to perform specific functions in transcriptional regulation, DNA repair, chromosome segregation and other fundamental processes. H2B.Z is a rare, apicomplexan-specific variant of histone H2B. Here we show that in Plasmodium falciparum H2B.Z localises to euchromatic intergenic regions throughout intraerythrocytic development and together with H2A.Z forms a double-variant nucleosomes subtype. more...
Organism:
Plasmodium falciparum 3D7
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL15857
6 Samples
Download data: GFF
Series
Accession:
GSE39702
ID:
200039702
2.

Representative Illumina sequencing libraries upon T7-polymerase based amplification

(Submitter supplied) This experiment highlights the extreme sequence bias generated by standard PCR amplication of sequencing libraries and decribes an adapted T7-polymerase based amplification method, which results in non-baised, representative libraries for Illumina sequencing
Organism:
Plasmodium falciparum 3D7
Type:
Other
Platform:
GPL10866
4 Samples
Download data: BED, GFF
Series
Accession:
GSE23868
ID:
200023868
3.

Epigenetic profile of the Plasmodium falciparum intraerythrocytic cycle

(Submitter supplied) This experiment characterizes the localisation of H2A.Z, H3K9ac and H3K4me3 in the epigenome of the human malaria parasite, P. falciparum at 4 different stages of intraerythrocytic development.
Organism:
Plasmodium falciparum 3D7
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL10866
17 Samples
Download data: BED, GFF
Series
Accession:
GSE23867
ID:
200023867
4.

Transcription profile of the Plasmodium falciparum intraerythrocytic cycle

(Submitter supplied) This experiment characterizes the transcriptome of the human malaria parasite, P. falciparum at 8 different stages of the intraerythrocytic cycle
Organism:
Plasmodium falciparum 3D7
Type:
Expression profiling by high throughput sequencing
Platform:
GPL10866
8 Samples
Download data: GFF, TXT
Series
Accession:
GSE23865
ID:
200023865
5.

H2A.Z Demarcates Intergenic Regions of the Plasmodium falciparum Epigenome That Are Dynamically Marked by H3K9ac and H3K4me3

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum 3D7
Type:
Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing; Other
Platform:
GPL10866
29 Samples
Download data: BED, GFF, TXT
Series
Accession:
GSE23787
ID:
200023787
6.

Actin-related protein Arp4 regulates euchromatic gene expression and development by H2A.Z deposition in blood-stage Plasmodium falciparum

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
36 Samples
Download data: BW
Series
Accession:
GSE143902
ID:
200143902
7.

Actin-related protein Arp4 regulates euchromatic gene expression and development by H2A.Z deposition in blood-stage Plasmodium falciparum [RNA-seq]

(Submitter supplied) Chromatin structure is a basal epigenetic mechanism that determines cellular fate by organizing the dynamic gene expression during the cell development and proliferation. The nuclear members of the evolutionarily conserved actin-related protein (ARPs) superfamily are major components of nucleosome remodelingcomplexes in the nucleus. In the human malaria parasites, Plasmodium falciparum, comparative genome analysis reveals that two canonical actins and three orthologues of ARPs including PfArp1, PfArp4, and PfArp6 are encoded in the genome of this parasite. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26835
18 Samples
Download data: TXT
Series
Accession:
GSE143901
ID:
200143901
8.

Actin-related protein Arp4 regulates euchromatic gene expression and development by H2A.Z deposition in blood-stage Plasmodium falciparum [H3K9ac ChIP-seq]

(Submitter supplied) Chromatin structure is a basal epigenetic mechanism that determines cellular fate by organizing the dynamic gene expression during the cell development and proliferation. The nuclear members of the evolutionarily conserved actin-related protein (ARPs) superfamily are major components of nucleosome remodelingcomplexes in the nucleus. In the human malaria parasites, Plasmodium falciparum, comparative genome analysis reveals that two canonical actins and three orthologues of ARPs including PfArp1, PfArp4, and PfArp6 are encoded in the genome of this parasite. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
4 Samples
Download data: BW
Series
Accession:
GSE143900
ID:
200143900
9.

Actin-related protein Arp4 regulates euchromatic gene expression and development by H2A.Z deposition in blood-stage Plasmodium falciparum [H2A.Z ChIP-seq]

(Submitter supplied) Chromatin structure is a basal epigenetic mechanism that determines cellular fate by organizing the dynamic gene expression during the cell development and proliferation. The nuclear members of the evolutionarily conserved actin-related protein (ARPs) superfamily are major components of nucleosome remodelingcomplexes in the nucleus. In the human malaria parasites, Plasmodium falciparum, comparative genome analysis reveals that two canonical actins and three orthologues of ARPs including PfArp1, PfArp4, and PfArp6 are encoded in the genome of this parasite. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
4 Samples
Download data: BW
Series
Accession:
GSE143899
ID:
200143899
10.

Actin-related protein Arp4 regulates euchromatic gene expression and development by H2A.Z deposition in blood-stage Plasmodium falciparum [Arp4/6 ChIP-seq]

(Submitter supplied) Chromatin structure is a basal epigenetic mechanism that determines cellular fate by organizing the dynamic gene expression during the cell development and proliferation. The nuclear members of the evolutionarily conserved actin-related protein (ARPs) superfamily are major components of nucleosome remodeling complexes in the nucleus. In the human malaria parasites, Plasmodium falciparum, comparative genome analysis reveals that two canonical actins and three orthologues of ARPs including PfArp1, PfArp4, and PfArp6 are encoded in the genome of this parasite. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
10 Samples
Download data: BW
Series
Accession:
GSE143898
ID:
200143898
11.

Histone variant H3.3 demarcates GC-rich coding and subtelomeric sequences and serves as a potential memory mark for virulence gene expression in P. falciparum

(Submitter supplied) ChIP-seq experiments were performed to profile PfH3.3 (PF3D7_0617900) in the malaria parasite Plasmodium falciparum. Sequencing of ChIP samples showed enrichment of PfH3.3 at GC-rich coding sequences and subtelomeric repetitive regions throughout the intraerythrocytic life cycle and additionally in intergenic regions during trophozoite stages. Also the promoter and the coding sequence of the active and poised var2CSA gene were marked (reference genome Plasmodium falciparum 3D7 from PlasmoDB version 6.1)
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL16607
12 Samples
Download data: BEDGRAPH
Series
Accession:
GSE80466
ID:
200080466
12.

P. falciparum Histone Occupancy Mapping

(Submitter supplied) Background: Epigenetic modifications of histones and regulation of chromatin structure have been implicated in regulation of virulence gene families in P. falciparum. To better understand chromatin-mediated gene regulation, we used a high-density oligonucleotide microarray to map the position and enrichment of nucleosomes across the entire genome of P. falciparum at three time points of the intra-erythrocytic developmental cycle (IDC) in vitro. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL9610
6 Samples
Download data: CEL, TXT
Series
Accession:
GSE18968
ID:
200018968
13.

Genome-wide localisation of histone variants in Toxoplasma gondii implicates variant exchange in transcriptional control by demarcation of functional chromatin regions (ChIP-seq)

(Submitter supplied) Chromatin is composed of DNA wrapped around nucleosomes, complexes consisting of highly basic proteins called histones. Histone variants are non-canonical variants of histones that have specific functions. The Apicomplexan parasite Toxoplasma gondii possesses conserved histone variants CenH3, H3.3, H2A.Z, H2A.X, as well as the parasite-specific H2B variant, H2BV (or H2B.Z). We surveyed the genome-wide distribution of T. more...
Organism:
Toxoplasma gondii RH
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL24058
23 Samples
Download data: BED, BROADPEAK, BW, NARROWPEAK
Series
Accession:
GSE104347
ID:
200104347
14.

Genome-wide localisation of histone variants in Toxoplasma gondii implicates variant exchange in transcriptional control by demarcation of functional chromatin regions

(Submitter supplied) Chromatin is composed of DNA wrapped around nucleosomes, complexes consisting of highly basic proteins called histones. Histone variants are non-canonical variants of histones that have specific functions. The Apicomplexan parasite Toxoplasma gondii possesses conserved histone variants CenH3, H3.3, H2A.Z, H2A.X, as well as the parasite-specific H2B variant, H2BV (or H2B.Z). We surveyed the genome-wide distribution of T. more...
Organism:
Toxoplasma gondii RH; Toxoplasma gondii ME49
Type:
Genome binding/occupancy profiling by genome tiling array
Platforms:
GPL15564 GPL15563
10 Samples
Download data: GFF, PAIR, TXT
Series
Accession:
GSE87834
ID:
200087834
15.

Genome-wide localisation of the bromodomain protein PfBDP1 in the malaria parasite P. falciparum

(Submitter supplied) During red-blood-cell-stage infection of Plasmodium falciparum, the parasite undergoes repeated rounds of replication, egress, and invasion. Erythrocyte invasion involves specific interactions between host cell receptors and parasite ligands and coordinated expression of genes specific to this step of the life cycle. We show that a parasite-specific bromodomain protein, PfBDP1, binds to chromatin at transcriptional start sites of invasion-related genes and directly controls their expression. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
22 Samples
Download data: TXT, XLS
Series
Accession:
GSE79135
ID:
200079135
16.

A Novel Plasmodium Falciparum Bromodomain Protein Regulates Invasion Gene Expression

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum; Plasmodium falciparum 3D7
Type:
Expression profiling by array; Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL11248 GPL21078
66 Samples
Download data: GPR
Series
Accession:
GSE64691
ID:
200064691
17.

Whole genome expression profiling across the life cycle of PfBDP1 overexpressing P. falciparum malaria parasites

(Submitter supplied) Erythrocyte invasion is an essential step in the life cycle of the malaria parasite Plasmodium falciparum that involves specific interactions between host cell receptors and parasite ligands. How the parasite regulates the expression of invasion-related genes is to date largely unknown. Here we show that a novel, parasite-specific bromodomain protein (PfBDP1) binds to chromatin at the transcriptional start site of invasion-related genes and directly controls their expression. more...
Organism:
Plasmodium falciparum 3D7; Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL11248
8 Samples
Download data: GPR
Series
Accession:
GSE64690
ID:
200064690
18.

Whole genome expression profiling across the asexual life cycle in PfBDP1 knockdown malaria parasites

(Submitter supplied) To study the bromodomain protein PfBDP1 in the malaria parasite P. falciparum, a transgenic parasite line was generated (PfBDP1DD) in which PfBDP1 was tagged with a haemagglutinin tag and a ligand regulatable FKBP destabilization domain that allowed conditional knockdown of PfBDP1 by removal of the stabilizing ligand Shld1 from cultures. Shld1 was removed 30 hours post invasion (hpi) and the cells allowed to reinvade fresh red blood cells. more...
Organism:
Plasmodium falciparum; Plasmodium falciparum 3D7
Type:
Expression profiling by array
Platform:
GPL11248
36 Samples
Download data: GPR
Series
Accession:
GSE64688
ID:
200064688
19.

Stepwise histone replacement by SWR1 requires dual activation with histone H2A.Z and canonical nucleosome

(Submitter supplied) Histone variant H2A.Z-containing nucleosomes are incorporated at most eukaryotic promoters. This incorporation is mediated by the conserved SWR1 complex, which replaces histone H2A in canonical nucleosomes with H2A.Z in an ATP-dependent manner. Here, we show that promoter-proximal nucleosomes are highly heterogeneous for H2A.Z in Saccharomyces cerevisiae, with substantial representation of nucleosomes containing one, two, or no H2A.Z molecules. more...
Organism:
Saccharomyces cerevisiae
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL11034
5 Samples
Download data: TXT
Series
Accession:
GSE24618
ID:
200024618
20.

Expression analysis of Plasmodium falciparum with MYST overexpression

(Submitter supplied) Investigation of genome-wide gene expression changes in Plasmodium falciparum overexpressing PfMYST compared to the wild-type strain 3D7. After introducing a single copy of the full-length PfMYST expression cassette into the parasite genome, parasites showed higher levels of H4-K5, -K8, and -K12 acetylation, a faster progression of intraerythrocytic developmental cycle (IDC), and shorter schizont development time (duration), which led to significantly fewer merozoites developed in mature schizonts than the control. more...
Organism:
Plasmodium falciparum; Plasmodium falciparum 3D7
Type:
Expression profiling by array
Platform:
GPL15768
12 Samples
Download data: PAIR, TXT
Series
Accession:
GSE245596
ID:
200245596
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