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Links from GEO DataSets

Items: 15

1.

ApiAP2 Factors as Candidate Regulators of Stochastic Commitment to Merozoite Production in Theileria annulata

(Submitter supplied) Investigation of parasite (T. annulata) gene expression over the course of the life-cycle (sporozoite->macroschizont->merozoite->piroplasm). The study focused on the expression of known and putative transcription factors, in particular members of the ApiAP2 gene family. Up-stream motifs associated with stage-specifically expressed genes were identified during the course of the analysis.
Organism:
Theileria annulata; Bos taurus
Type:
Expression profiling by array
Platform:
GPL20733
20 Samples
Download data: TXT
Series
Accession:
GSE71307
ID:
200071307
2.

Transcriptomic analysis of Plasmodium berghei apiAP2 KO mutants

(Submitter supplied) During the progress through its complex life cycle, the malaria parasite requires strict control of gene expression but the mechanism controlling this process remain poorly understood and unexplored for therapeutic purposes. A group of the apicomplexa-specific putative transcription factors with AP2 DNA binding domain (apiAP2) has been identified as the major regulators of the parasite transcriptome at multiple stages. more...
Organism:
Plasmodium berghei
Type:
Expression profiling by high throughput sequencing
Platform:
GPL20293
62 Samples
Download data: TXT
Series
Accession:
GSE80634
ID:
200080634
3.

Identification of antimalarial compounds that inhibit Apicomplexan AP2 transcription factor proteins in the human malaria parasite Plasmodium falciparum [ChIP-seq]

(Submitter supplied) Plasmodium parasites are reliant on the Apicomplexan AP2 (ApiAP2) transcription factor family to regulate gene expression programs. AP2 DNA binding domains have no homologs in the human or mosquito host genomes, making them potential antimalarial drug targets. Using an in-silico screen to dock thousands of small molecules into the crystal structure of the AP2-EXP (Pf3D7_1466400) AP2 domain (PDB:3IGM), we identified compounds that interact with this domain. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21078 GPL26920
8 Samples
Download data: BIGWIG, NARROWPEAK
Series
Accession:
GSE208155
ID:
200208155
4.

Plasmodium berghei Gametocytogenesis

(Submitter supplied) Transcriptional profiling of gametocyte non-producer lines in Plasmodium berghei Transcriptome of gametocyte non producer lines (natural and genetic KO) and parental (820) lines. The aim of the study was to identify key genes involved in the decision to commit to gametocytogenesis in Plasmodium berghei. These microarrays compare naturally selected lines that do not produce gametocytes, and the parental line and additionally a genetic knock out of AP2-G PBANKA_143750. more...
Organism:
Plasmodium berghei
Type:
Expression profiling by array
Platform:
GPL18005
28 Samples
Download data: TXT
Series
Accession:
GSE53246
ID:
200053246
5.

Differential gene expression in ap2-g and ap2-g2 mutants of Plasmodium berghei

(Submitter supplied) Commitment to and completion of sexual development are essential for malaria parasites to be transmitted through mosquitoes. The molecular mechanism(s) responsible for these processes however, remain largely unknown. We have identified two transcription factors (both belonging to the AP2 family) essential for gametocytogenesis. AP2-G mutants are characterised by a complete inability to produce gametocytes. more...
Organism:
Plasmodium berghei
Type:
Expression profiling by array
Platform:
GPL18005
8 Samples
Download data: TXT
Series
Accession:
GSE52859
ID:
200052859
6.

Effect of AP2IX-9 overexpression on CTG transcriptome upon alkaline treatment

(Submitter supplied) Overexpression of DDHA-AP2IX-9 under a tubulin promoter in type III CTG strain. Differential expression analysis under addition of shield-1 and comparison to the non-bradyzoite induced parental culture revealed a global downregulation of the bradyzoite gene expression program including canonical markers like BAG1.
Organism:
Toxoplasma gondii
Type:
Expression profiling by array
Platform:
GPL16542
11 Samples
Download data: CEL
Series
Accession:
GSE36300
ID:
200036300
7.

ChIP-seq data analysis of TgAP2XII-1 on the whole genome of Toxoplasma gondii tachyzoites [XII-1 ChIPseq]

(Submitter supplied) Transcriptomic analyses revealed the gene expression changes after AP2XII-1 depletion. To see which of these differentially expressed genes are directly targeted by AP2XII-1, we used chromatin immunoprecipitation, followed by deep sequencing (ChIP-Seq) to assess the binding positions of AP2XII-1 in the parasite’s genome.
Organism:
Toxoplasma gondii
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL33297
4 Samples
Download data: BW
Series
Accession:
GSE228581
ID:
200228581
8.

RNA-seq data analysis of TgAP2XII-1 on Toxoplasma gondii merozoites development [ME49 XII-1 RNAseq]

(Submitter supplied) To investigate transcriptional role of TgAP2XII-1 on type II Toxoplasma gondii (ME49 Tir1), an auxin inducible degron system was introduced to control the protein expression of TgAP2XII-1 and the target protein could be totally degradated in 3h after adding IAA.
Organism:
Toxoplasma gondii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33297
6 Samples
Download data: TXT
Series
Accession:
GSE228580
ID:
200228580
9.

RNA-seq data analysis of TgAP2XII-1 on Toxoplasma gondii merozoites development

(Submitter supplied) To investigate transcriptional role of TgAP2XII-1 on type I Toxoplasma gondii (RHΔhxgprt Tir1), an auxin inducible degron system was introduced to control the protein expression of TgAP2XII-1 and the target protein could be totally degradated in 3h after adding IAA.
Organism:
Toxoplasma gondii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL33110
9 Samples
Download data: TXT
Series
Accession:
GSE224934
ID:
200224934
10.

The transcription factor AP2XI-2 is a key negative regulator of Toxoplasma gondii merogony

(Submitter supplied) Commitment to and completion of sexual development are essential for Toxoplasma gondii to produce oocysts in the intestine of the feline host. Understanding of the molecular mechanism responsible for sexual commitment is extremely limited due to the lack of model systems. Here, we show that the transcription factors AP2XI-2 and AP2XII-1 associated with the epigenetic repressors MORC/HDAC3 complex are constitutively expressed in both tachyzoite and bradyzoite stages but not in the merozoite stage. more...
Organism:
Toxoplasma gondii
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26742
6 Samples
Download data: BW
Series
Accession:
GSE248448
ID:
200248448
11.

A coordinated regulatory network of ApiAP2 transcription factors involved in heterochromatic gene expression during Plasmodium falciparum blood-stage development

(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
192 Samples
Download data: BED, BW
Series
Accession:
GSE184659
ID:
200184659
12.

A coordinated regulatory network of ApiAP2 transcription factors involved in heterochromatic gene expression during Plasmodium falciparum blood-stage development [ChIP-Seq]

(Submitter supplied) Genome-wide occupancy of sixteen PfApiAP2 transcription factors and PfHP1 throughout the intraerythrocytic cycle
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
144 Samples
Download data: BED, BW
Series
Accession:
GSE184658
ID:
200184658
13.

A coordinated regulatory network of ApiAP2 transcription factors involved in heterochromatic gene expression during Plasmodium falciparum blood-stage development [RNA-Seq]

(Submitter supplied) Effects of PfApiAP2 knockouts on gene expression in the intraerythrocytic cycle
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26835
48 Samples
Download data: CSV
Series
Accession:
GSE184645
ID:
200184645
14.

Transgenic Plasmodium falciparum parasites line 3D7/DDGFP-PfAP2-HC: transcriptional differences between 3D7/DDGFP-PfAP2-HC control parasites (cultured in presence of Shield-1; ON) vs PfAP2-HC-depleted parasites (cultured in absence of Shield-1; OFF)

(Submitter supplied) Transcriptional profiling of transgenic P. falciparum asexual blood stage parasites of the transgenic strain 3D7/DDGFP-PfAP2-HC at five time points during intra-erythrocytic parasite development. The DD (FKBP destabilisation domain) allows for the conditional expression of fusion proteins: DD fusion proteins are rapidly degraded or stably expressed in absence or presence of the stabilising ligand Shield-1, respectively (Banaszynski LA, Chen LC, Maynard-Smith LA, Ooi AG, Wandless TJ. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
10 Samples
Download data: GPR
Series
Accession:
GSE159061
ID:
200159061
15.

PfAP2-HC, an unusual, heterochromatin-associated ApiAP2 factor of Plasmodium falciparum

(Submitter supplied) In this study we have investigated PfAP2-HC (PF3D7_1456000), a protein that was identified by co-immunoprecipitation with PfHP1 coupled with liquid chromatography-tandem mass spectrometry. PfAP2-HC belongs to the ApiAP2 family, the main transcription factor family in Apicomplexan parasites. We have confirmed that AP2-HC colocalises with HP1 with the use of immunofluorescence assays and chromatin immunoprecipitation-sequencing. more...
Organism:
Plasmodium falciparum 3D7
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25935
17 Samples
Download data: BEDGRAPH
Series
Accession:
GSE154840
ID:
200154840
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