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Links from GEO DataSets

Items: 19

1.

The HAT Inhibitor Anacardic Acid Leads to Changes in Global Gene Expression During in vitro P.falciparum Development

(Submitter supplied) To better understand the role of histone lysine acetylation in transcription in Plasmodium falciparum, we sought to attenuate the histone acetyltransferase (HAT) activity of PfGCN5 using anacardic acid (AA). We showed that AA reversibly and noncompetitively inhibited the HAT activity of recombinant PfGCN5. To a lesser extent, AA inhibited the PfGCN5 activity in parasite nuclear extracts, but did not affect the histone deacetylase activity. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1858
9 Samples
Download data: TXT
Series
Accession:
GSE11763
ID:
200011763
2.

Global transcriptional changes upon Bromodomain (BrD) deletion in PfGCN5 and PHD domain deletion in PfPHD1 by transcriptome analyses via RNA-seq

(Submitter supplied) Purpose: In malaria parasite, PfGCN5, a histone acetyltansferase (HAT),forms a unique complex including a PHD domain containing protein named PfPHD1. To understand the function of this complex, the BrD in PfGCN5 and PHD in PfPHD1 were deleted. The transcritional changes after domain deletions were measured by RNA-seq. Methods: The mRNA profiles of parasite lines : 3D7 (WT), PfGCN5-ΔBrD and PfPHD1-ΔPHD, were generated by deep sequencing, in triplicate, using Illumina HiSeq 2500 in Rapid Run mode using 100nt single read sequencing. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21078
36 Samples
Download data: XLSX
Series
Accession:
GSE164070
ID:
200164070
3.

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
4.

Transcriptional profiling defines histone acetylation as a regulator of gene expression during human-to-mosquito transmission of the malaria parasite Plasmodium falciparum

(Submitter supplied) Transmission of the malaria parasite Plasmodium falciparum from the human to the mosquito is mediated by the intraerythrocytic gametocytes, which, once taken up during a blood meal, become activated to initiate sexual reproduction. Because gametocytes are the only parasite stages able to establish an infection in the mosquito, they are crucial for spreading the tropical disease. During gametocyte maturation, different repertoires of genes are switched on and off in a well-coordinated sequence, pointing to regulatory mechanisms of gene expression. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
12 Samples
Download data: TXT
Series
Accession:
GSE99223
ID:
200099223
5.

Pan-AcH4 ChIP-chip with High Resolution Tiling Arrays on HUVECs and HuAoVSMCs

(Submitter supplied) Differential EC enrichment of pan-AcH4 was assessed at 34 select genes, including 19 EC-enriched genes, 6 broadly expressed genes, and 9 EC-excluded genes, by pan-AcH4 (AcH4K5, AcH4K8, AcH4K12, and AcH4K16) ChIP-chip analysis on human umbilical vein endothelial cells (HUVECs) and human aortic vascular smooth muscle cells (HuAoVSMCs) with a high resolution tiling DNA microarray. Specifically, the tiling array analyzes the 50 kb genomic region upstream of transcription initiation, the intragenic regions , and 50 kb genomic region downstream of the last exon.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL22952
6 Samples
Download data: TXT
Series
Accession:
GSE93962
ID:
200093962
6.

Pan-AcH3 ChIP-chip with Custom High Resolution Tiling Arrays on HUVECs and HuAoVSMCs

(Submitter supplied) Differential EC enrichment of pan-AcH3 was assessed at 34 select genes, including 19 EC-enriched genes, 6 broadly expressed genes, and 9 EC-excluded genes, by pan-AcH3 (AcH3K9 and AcH3K14) ChIP-chip analysis on human umbilical vein endothelial cells (HUVECs) and human aortic vascular smooth muscle cells (HuAoVSMCs) with a high resolution tiling DNA microarray. Specifically, the tiling array analyzes the 50 kb genomic region upstream of transcription initiation, the intragenic regions, and 50 kb genomic region downstream of the last exon.
Organism:
Homo sapiens
Type:
Genome binding/occupancy profiling by genome tiling array
Platform:
GPL22952
4 Samples
Download data: TXT
Series
Accession:
GSE93868
ID:
200093868
7.

Comparison of HBO1 siRNA-treated Human Umbilical Vein Endothelial Cells (HUVECs) and control siRNA-treated HUVECs

(Submitter supplied) To determine the role of HBO1 in EC physiology, gene expression analysis was conducted on control and HBO1 siRNA-treated HUVECs. A total of 263 differentially regulated protein-coding transcripts were detected, many of which are key for growth and angiogenesis. Additionally, many genes involved in cell cycle, cell division, and DNA replication were dysregulated. HBO1-regulated genes were verified by qRT-PCR, including those with roles in vessel tone regulation (e.g. more...
Organism:
Homo sapiens
Type:
Expression profiling by array; Non-coding RNA profiling by array
Platform:
GPL16956
8 Samples
Download data: TXT
Series
Accession:
GSE93608
ID:
200093608
8.

Effect of growth in TSA or SCFA on gene expression in E. histolytica

(Submitter supplied) In order to dtermine the role of histone actylation in gene expresssion, E. histolytica 200:NIH trophozoites were treated with the HDAC inhibitor Trichostatin A, or grown in short chain fatty acids, which have been shown to alter histone actylation patterns in Entamoeba species. Keywords: Expression
Organism:
Entamoeba histolytica
Type:
Expression profiling by array
Platform:
GPL4622
8 Samples
Download data: CEL
Series
Accession:
GSE8047
ID:
200008047
9.

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
10.

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
11.

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
12.

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
13.

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
14.

Expression and genomic changes after exposing drug-selected mutants to short term CQ treatment in Plasmodium falciparum.

(Submitter supplied) Mutations in PfCRT confer chloroquine (CQ) resistance in P. falciparum. Point mutations in the homolog of the mammalian multidrug resistance gene (pfmdr1) can also modulate the levels of CQ response. However, parasites with the same pfcrt and pfmdr1 alleles exhibit a wide range of drug sensitivity, suggesting that additional genes contribute to levels of CQ resistance (CQR). We used 3 isogenic lines which have different drug resistance profiles corresponding to unique mutations in the pfcrt gene (106/1K76, 106/176I, and 106/76I-352K) to study changes in gene expression with and without CQ and genomic variations, i.e. more...
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array; Genome variation profiling by array
Dataset:
GDS3284
Platform:
GPL1321
24 Samples
Download data: CEL
Series
Accession:
GSE10022
ID:
200010022
15.
Full record GDS3284

Antimalarial drug chloroquine effect on PfCRT mutant parasite lines

Analysis of Plasmodium falciparum chloroquine-resistant transporter (PfCRT) mutants exposed to a low dose of chloroquine (CQ) for 3 h. The clones have different degrees of CQ resistance (CQR). Results provide insight into the molecular basis of the PfCRT effect on parasite susceptibility to CQ.
Organism:
Plasmodium falciparum; Anopheles gambiae
Type:
Expression profiling by array, transformed count, 2 agent, 3 genotype/variation sets
Platform:
GPL1321
Series:
GSE10022
18 Samples
Download data: CEL
16.

Genome-wide map of H4K8ac in Plasmodium falciparum

(Submitter supplied) P. falciparum H4K8ac ChIP-seq
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL16607 GPL19269
8 Samples
Download data: TXT
Series
Accession:
GSE93145
ID:
200093145
17.

Role of H4K8ac in P. falciparum life cycle

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array; Genome variation profiling by array
Platforms:
GPL11250 GPL11248
135 Samples
Download data: GPR
Series
Accession:
GSE84084
ID:
200084084
18.

Role of H4K8ac in P. falciparum life cycle [ChIP]

(Submitter supplied) Study of chromatin changes of P. falciparum in response to changes in the levels of histone H4 acetylations especially H4K8ac using chromatin immunoprecipitation coupled to microarray chip (ChIP-on-chip)
Organism:
Plasmodium falciparum
Type:
Genome variation profiling by array
Platform:
GPL11250
39 Samples
Download data: GPR, TXT
Series
Accession:
GSE84083
ID:
200084083
19.

Role of H4K8ac in P. falciparum life cycle [gene expression]

(Submitter supplied) Transcriptional analaysis of P. falciparum in response to changes in the levels of histone H4 acetylations especially H4K8ac
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL11248
96 Samples
Download data: GPR, TXT
Series
Accession:
GSE84082
ID:
200084082
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