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Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G [ChIP-seq]

ABSTRACT: Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G [ChIP-seq]

PROVIDER: PRJNA605466 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR11043317.fastq.gz	Fastqsanger.gz
	SRR11043318.fastq.gz	Fastqsanger.gz
	SRR11043320.fastq.gz	Fastqsanger.gz
	SRR11043321.fastq.gz	Fastqsanger.gz

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Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G

Project description:Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G

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Project description:Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G [ChIP-seq]

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Project description:Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G [DIP-seq]

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Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G [DIP-seq]

Project description:AP2-G is a transcription factor (TF) that is essential for gametocytogenesis of malaria parasites; however, the mechanisms for its inducing the cell linage for sexual reproduction remain unclear. In this paper, this problem is addressed by investigating its expression profile and by determining target genes genome-wide in Plasmodium berghei.

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Mechanisms of Triggering Malaria Gametocytogenesis by AP2-G

Project description:This SuperSeries is composed of the SubSeries listed below.

2021-02-01 | GSE144971 | GEO

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

Project description: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. In AP2-G2 mutants the gametocytaemia is very significantly reduced but not completely abolished. We have performed the microarray experiments in order to cokmpare the transcriptomes of these mutantnts to the WT parasites and between each other. As P.berghei parasites are characterised by asynchronous development in the rodent host, the different stage composition of the sample would impact the analysis. Therefore parasites were harvested and matured in in vitro to the schizont stage Pairwaise comparison between the mutants and parental line was performed. 3 biological replicates of each condition were used.

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

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