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Links from GEO DataSets

Items: 20

1.

PfAP2-G ChIP-seq in stage I gametocytes derived via next cycle conversion (NCC) and same cycle conversion (SCC)

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. Here we identify for the first time the direct targets of PfAP2-G and demonstrate that it dynamically binds hundreds of sites across the genome. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26920
8 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE134268
ID:
200134268
2.

Regulation of sexual differentiation is linked to invasion in malaria parasites

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array; Genome binding/occupancy profiling by high throughput sequencing
Platforms:
GPL21078 GPL15130
62 Samples
Download data: BED, BIGWIG, TXT
Series
Accession:
GSE125566
ID:
200125566
3.

PfAP2-G target gene promoter mutants expression timecourse

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. We show conclusively that PfAP2-G is a transcriptional activator of gametocyte genes and identify the earliest known markers expressed during commitment. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
22 Samples
Download data: TXT
Series
Accession:
GSE121312
ID:
200121312
4.

PfAP2-G DD +Shld1 vs. -Shld1 expression timecourse

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. We show conclusively that PfAP2-G is a transcriptional activator of gametocyte genes and identify the earliest known markers expressed during commitment. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
22 Samples
Download data: TXT
Series
Accession:
GSE120990
ID:
200120990
5.

PfAP2-G and PfAP2-I ChIP-seq in schizonts

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch that occurs from asexual multiplication to sexual differentiation is essential for transmission to mosquitos. One of the key drivers of commitment to sexual development is the transcription factor AP2-G. Although it has been hypothesised that AP2-G orchestrates this crucial cell fate decision by driving expression of gametocyte genes, the molecular mechanisms by which this occurs remain unknown. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
6 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE120488
ID:
200120488
6.

PfAP2-G ChIP-seq in committed schizonts, sexual rings, and stage I gametocytes

(Submitter supplied) In the malaria parasite Plasmodium falciparum, the switch from asexual multiplication to sexual differentiation into gametocytes is essential for transmission to mosquitos. One of the key determinants of sexual commitment is the transcription factor PfAP2-G, which has been proposed to orchestrate this crucial cell fate decision by driving expression of gametocyte genes. We show conclusively that PfAP2-G is a transcriptional activator of gametocyte genes and identify the earliest known markers expressed during commitment. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
12 Samples
Download data: BED, BIGWIG
Series
Accession:
GSE120448
ID:
200120448
7.

Comparison of Gametocyte producer 3D7-A subclone E5 to the gametotcyte nonprodcer strain F12 and pfap2-g deletion mutant

(Submitter supplied) Identify differentially expressed genes across the 48h intraerythrocytic development cycle of gametocyte non-producers of P. falcuparum
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL17880
32 Samples
Download data: TXT
Series
Accession:
GSE52030
ID:
200052030
8.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [WGS-Seq]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome variation profiling by high throughput sequencing
Platform:
GPL26835
4 Samples
Download data: XLSX
Series
Accession:
GSE175931
ID:
200175931
9.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [ChIP-Seq HM]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
12 Samples
Download data: BW
Series
Accession:
GSE157709
ID:
200157709
10.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5)

(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
117 Samples
Download data: BW
Series
Accession:
GSE149774
ID:
200149774
11.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [ChIP-Seq TF]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL26835
18 Samples
Download data: BED, BW
Series
Accession:
GSE149773
ID:
200149773
12.

A transcriptional repressor programs gametocytogenesis in human malaria parasites (PfAP2-G5) [RNA-Seq]

(Submitter supplied) Gametocytogenesis, the process by which malaria parasites produce sexual forms that can infect mosquitoes, is essential for the transmission of malaria. A transcriptional switch of the pfap2-g gene triggers sexual commitment, but how the complex multi-step process is precisely programed remains largely unknown. Here, by systematic functional screening of a panel of ApiAP2 transcription factors, we identify six new apiAP2 members associated with gametocytogenesis in Plasmodium falciparum. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platform:
GPL26835
83 Samples
Download data: XLSX
Series
Accession:
GSE149772
ID:
200149772
13.

The PfAP2-G2 transcription factor is a critical regulator of gametocyte maturation

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
44 Samples
Download data: TXT
Series
Accession:
GSE160937
ID:
200160937
14.

Plasmodium falciparum PfAP2-G2 KO gametocyte microarray timecourse

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human to the mosquito host. Preventing gametocyte commitment and development would block parasite transmission, but the underlying molecular mechanisms behind these processes remain poorly understood. Here, we report that the ApiAP2 transcription factor, PfAP2-G2 (PF3D7_1408200) plays a critical role in the maturation of Plasmodium falciparum gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
28 Samples
Download data: TXT
Series
Accession:
GSE160924
ID:
200160924
15.

Plasmodium falciparum PfAP2-G2 KO asexual microarray timecourse

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human to the mosquito host. Preventing gametocyte commitment and development would block parasite transmission, but the underlying molecular mechanisms behind these processes remain poorly understood. Here, we report that the ApiAP2 transcription factor, PfAP2-G2 (PF3D7_1408200) plays a critical role in the maturation of Plasmodium falciparum gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
16 Samples
Download data: TXT
Series
Accession:
GSE160923
ID:
200160923
16.

ChIP-seq on PfAP2-G2 in trophozoite and gametocyte stages of parasites.

(Submitter supplied) Differentiation from asexual blood stages to sexual gametocytes is required for transmission of malaria parasites from the human host to mosquitos, where sexual fertilization occurs to complete the lifecycle. Although preventing gametocyte development would block parasite transmission, the molecular mechanisms underlying sexual commitment and gametocyte maturation are still relatively unknown. Previous studies identified an ApiAP2 protein, AP2-G2, which plays a critical role in gametocyte maturation in rodent malaria parasite Plasmodium berghei by acting as the repressor of asexual stage genes in gametocytes. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21298
10 Samples
Download data: BIGWIG
Series
Accession:
GSE157753
ID:
200157753
17.

Identification of a subtelomeric gene family expressed during the asexual-sexual stage transition in Plasmodium falciparum

(Submitter supplied) For malaria transmission, the parasite must undergo sexual differentiation into mature gametocytes. However, the molecular basis for this critical transition in the parasites life cycle is unknown. Six previously uncharacterized genes, Pfg14.744, Pfg14.745, Pfg14.748, Pfg14.763, Pfg14.752 and Pfg6.6 that are members of a 36 gene Plasmodium falciparum-specific subtelomeric superfamily were found to be expressed in parasites that are committed to sexual development as suggested by co-expression of Pfs16 and Pfg27. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL1858
8 Samples
Download data: GPR
Series
Accession:
GSE62364
ID:
200062364
18.

PfAP2-I-GFP anti-GFP and anti-IgG ChIP-seq

(Submitter supplied) To determine the genome-wide occupancy of the Plasmodium falciparum transcriptional regulator of invasion PfAP2-I (PfDd2_100013100/PF3D7_1007700), we used chromatin immunoprecipitation coupled with next-generation sequencing (ChIP-seq). Synchronized, schizont stage, 40 hours post-invasion, cultures of parasites expressing the AP2-I-GFP fusion protein were treated with formaldehyde to crosslink proteins to DNA and harvested. more...
Organism:
Plasmodium falciparum
Type:
Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL21078
9 Samples
Download data: BEDGRAPH
Series
Accession:
GSE80293
ID:
200080293
19.

Transcriptomic analysis of heat shock resistance in Plasmodium falciparum

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platforms:
GPL28456 GPL11248
45 Samples
Download data: GPR, TXT
Series
Accession:
GSE149394
ID:
200149394
20.

Transcriptional alterations of P. falciparum 3D7-A heat shock-adapted vs control parasites.

(Submitter supplied) Periodic fever is the most characteristic clinical feature of human malaria. However, how parasites survive malarial febrile episodes, which often involve temperatures of >40ºC, is not known. To understand the molecular basis of heat shock (HS) resistance in Plasmodium falciparum, we took advantage of previously developed P. falciparum lines adapted to periodic HS (3D7-A-HS) and their non-selected controls maintained in parallel (3D7-A). more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL11248
24 Samples
Download data: GPR, XLS
Series
Accession:
GSE149393
ID:
200149393
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