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Links from GEO DataSets

Items: 20

1.

5-methylcytosine modification-mediated mRNA stabilization is associated with sexual development of malaria parasites

(Submitter supplied) This SuperSeries is composed of the SubSeries listed below.
Organism:
Plasmodium falciparum; Plasmodium yoelii
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL26836 GPL29225
36 Samples
Download data: XLS
Series
Accession:
GSE159127
ID:
200159127
2.

5-methylcytosine modification-mediated mRNA stabilization is associated with sexual development of malaria parasites [BisRNA-seq]

(Submitter supplied) 5-methylcytosine (m5C) is emerging as an important epi-transcriptome modification involving RNA stability and translation efficiency in various biological processes. However, it remains unclear how m5C contributes to the dynamic regulation of transcriptome during the development of Plasmodium. Here, we identified the presence of 5-methylcytosine (m5C) modification in rodent (P. yoelii) and human (P. more...
Organism:
Plasmodium yoelii; Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing; Methylation profiling by high throughput sequencing
Platforms:
GPL26836 GPL29225
14 Samples
Download data: TXT, XLSX
Series
Accession:
GSE159126
ID:
200159126
3.

5-methylcytosine modification-mediated mRNA stabilization is associated with sexual development of malaria parasites [Half-life]

(Submitter supplied) 5-methylcytosine (m5C) is emerging as an important epi-transcriptome modification involving RNA stability and translation efficiency in various biological processes. However, it remains unclear how m5C contributes to the dynamic regulation of transcriptome during the development of Plasmodium. Here, we identified the presence of 5-methylcytosine (m5C) modification in rodent (P. yoelii) and human (P. more...
Organism:
Plasmodium yoelii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL29225
8 Samples
Download data: TXT
Series
Accession:
GSE159125
ID:
200159125
4.

5-methylcytosine modification-mediated mRNA stabilization is associated with sexual development of malaria parasites [RNA-seq]

(Submitter supplied) 5-methylcytosine (m5C) is emerging as an important epi-transcriptome modification involving RNA stability and translation efficiency in various biological processes. However, it remains unclear how m5C contributes to the dynamic regulation of transcriptome during the development of Plasmodium. Here, we identified the presence of 5-methylcytosine (m5C) modification in rodent (P. yoelii) and human (P. more...
Organism:
Plasmodium yoelii; Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL26836 GPL29225
14 Samples
Download data: TXT
Series
Accession:
GSE159124
ID:
200159124
5.

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
6.

PFNF54-Pfs16-GFP-LUC gametocyte time course from commitment to maturity

(Submitter supplied) Plasmodium falciparum gametocytes undergo 14 days of gametocytogenesis to generate mature, transmissible gametocytes. This timecourse delineates the transcriptional profiles of gametocytes from commitment to maturity.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
16 Samples
Download data: TXT
Series
Accession:
GSE104889
ID:
200104889
7.

Transcriptome-wide dynamics of extensive m6A mRNA methylation during Plasmodium falciparum blood-stage development

(Submitter supplied) Malaria pathogenesis results from the asexual replication of Plasmodium falciparum within human red blood cells, which relies on a precisely timed cascade of gene expression over a 48-hour life cycle. However, post-transcriptional control of this hardwired program has been largely unexplored. To this end, we performed a comprehensive characterization of m6A mRNA methylation during the different developmental stages. more...
Organism:
Plasmodium falciparum 3D7
Type:
Expression profiling by high throughput sequencing; Genome binding/occupancy profiling by high throughput sequencing
Platform:
GPL25935
14 Samples
Download data: BED, BEDGRAPH, TXT
Series
Accession:
GSE123839
ID:
200123839
8.

Puf3 participates in ribosomal biogenesis in malaria parasites

(Submitter supplied) Recent studies of the Puf family of RNA-binding proteins revealed that besides their traditional roles in translational regulation of mRNAs, some Puf proteins are also involved in ribosome biogenesis by binding rRNA. In this study, we report the role of a Puf-like protein in Plasmodium falciparum (name as PfPuf3) and its ortholog PyPuf3 in Plasmodium yoelii in ribosome biogenesis. Secondary structure prediction suggested that the RNA-binding domain of Puf3 consists of 11 pumilio repeats, similar to human Puf-A/yeast Puf6, which involved in ribosome biogenesis. more...
Organism:
Plasmodium falciparum
Type:
Other
Platform:
GPL21078
4 Samples
Download data: TXT
Series
Accession:
GSE105126
ID:
200105126
9.

The DEAD-box RNA helicase PfDOZI imposes opposing actions on RNA metabolism in Plasmodium falciparum

(Submitter supplied) Purpose: In malaria parasites, the regulation of mRNA translation, storage and degradation is a critical aspect of gene expression, especially during the life stage transition. Since the DEAD-box helicases are involved in RNA metabolism, we wanted to determine whether pfdozi disruption led to altered mRNA abundance in P. falciparum. Methods: In this study, we functionally characterized the DEAD-box RNA helicase PfDOZI in the human malaria parasite Plasmodium falciparum and discovered its functions on mRNA metabolism during development. more...
Organism:
Plasmodium falciparum
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL21078 GPL19269
44 Samples
Download data: FASTA, XLSX
Series
Accession:
GSE189034
ID:
200189034
10.

Whole genome transcriptome profiling of P. falciparum sexually comitted ring stage parasite from malaria patient's peripheral blood

(Submitter supplied) Malaria is spread by the transmission of sexual stage parasites, called gametocytes. However, with Plasmodium falciparum, gametocytes can only be detected in peripheral blood when they are mature and transmissible to a mosquito, which complicates control efforts. Here, we identify the set of genes overexpressed in patient blood samples with high levels of gametocyte-committed ring stage parasites. Expression of all 18 genes was regulated by transcription factor AP2-G, which is required for gametocytogenesis. more...
Organism:
Plasmodium falciparum; Homo sapiens
Type:
Expression profiling by array
Platform:
GPL15130
24 Samples
Download data: TXT
Series
Accession:
GSE152536
ID:
200152536
11.

Multiple links between 5-methylcytosine content of mRNA and translation

(Submitter supplied) 5-methylcytosine (m5C) is a prevalent base modification in tRNA and rRNA but it also occurs more broadly in the transcriptome, including in mRNA. In pursuit of potential links of m5C with mRNA translation, we performed polysome profiling of human HeLa cell lysates and subjected RNA from resultant fractions to efficient bisulfite conversion followed by RNA sequencing (bsRNA-seq). Bioinformatic filters for rigorous site calling were devised to reduce technical noise. more...
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing; Other
Platform:
GPL16791
12 Samples
Download data: XLSX
Series
Accession:
GSE140995
ID:
200140995
12.

Mapping of m6A and m5C on HIV with PA-antibody-seq

(Submitter supplied) In this GEO submission we include the PA-m6A-seq and PA-m5C-seq datasets for HIV in CEM & 293T cells
Organism:
Human immunodeficiency virus
Type:
Expression profiling by high throughput sequencing; Other
Platform:
GPL26648
11 Samples
Download data: BED
Series
Accession:
GSE130972
ID:
200130972
13.

Extensive Transcriptional and Translational Regulation Occur During the Maturation of Malaria Parasite Sporozoites

(Submitter supplied) These data were used to assess gene expression and dynamics between oocyst sporozoites and salivary gland sporozoites for both Plasmodium falciparum and Plasmodium yoelii.
Organism:
Plasmodium falciparum 3D7; Plasmodium yoelii yoelii 17XNL
Type:
Expression profiling by high throughput sequencing
Platforms:
GPL24926 GPL23784
12 Samples
Download data: XLSX
Series
Accession:
GSE113582
ID:
200113582
14.

mRNA bisulfite-sequencing of pancreatic cancer cells

(Submitter supplied) 5-methylcytosine sites of mRNA in BxPC-3, PANC1, and MiaPaCa-2 pancreatic cancer cells at the single-base resolution by whole-transcriptome bisulfite sequencing.
Organism:
Homo sapiens
Type:
Methylation profiling by high throughput sequencing; Other
Platform:
GPL18573
15 Samples
Download data: XLSX
Series
Accession:
GSE182148
ID:
200182148
15.

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
16.

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
17.

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
18.

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
19.

Capturing the dynamic RNA landscape of the malaria parasite P. falciparum

(Submitter supplied) To date, total mRNA analysis throughout intraerythrocytic development of the malaria parasite, Plasmodium falciparum, has only revealed abundance profiles of each gene at a given time. Here, we establish a new methodology in Plasmodium falciparum that enables biosynthetic labeleing and capture of sub-population mRNA. As a proof of principle for this novel method, we examine the mRNA dynamics of early gametocyte commitment.
Organism:
Plasmodium falciparum
Type:
Expression profiling by array
Platform:
GPL15130
48 Samples
Download data: TXT
Series
Accession:
GSE72695
ID:
200072695
20.

Comparative Total RNA-seq between WT and alba4-null Plasmodium yoelii parasites

(Submitter supplied) To determine the role of ALBA4 in mRNA homeostasis in Plasmodium parasites, we performed comparative total RNA-seq between a WT-GFP line and an alba4-null line. We performed these experiments at three points in the life cycle - asexual (schizont), sexual (gametocyte), and oocyst sporozoite stages. We found that ALBA4 has a multi-faceted role in mRNA homeostasis, and is involved in mRNA fate determination. more...
Organism:
Plasmodium yoelii
Type:
Expression profiling by high throughput sequencing
Platform:
GPL21940
16 Samples
Download data: XLSX
Series
Accession:
GSE81834
ID:
200081834
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