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Plasmodium falciparum

ABSTRACT: Plasmodium falciparum pooled sequencing

PROVIDER: PRJNA260844 | ENA |

REPOSITORIES: ENA

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Dataset's files

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			Action	DRS
	SRR1573910_1.fastq.gz	Fastqsanger.gz
	SRR1573910_2.fastq.gz	Fastqsanger.gz
	SRR1573921_1.fastq.gz	Fastqsanger.gz
	SRR1573921_2.fastq.gz	Fastqsanger.gz
	SRR1573923_1.fastq.gz	Fastqsanger.gz

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Discovery of telomere repeat-binding factor in the malaria parasite Plasmodium falciparum

Project description:ChIP-seq experiments were performed for the putative telomere repeat-binding factor (PfTRF) in the malaria parasite Plasmodium falciparum strain 3D7. The gene encoding this factor (PF3D7_1209300) was endogenously tagged with either a GFP- or a 3xHA-tag and these transgenic parasite lines were used in ChIP-sequencing experiments. Sequencing of the ChIP and input libraries showed enrichment of PfTRF at all telomere-repeat containing chromosome ends (reference genome Plasmodium falciparum 3D7 from PlasmoDB version 6.1) as well as in all upsB var promoters.In addition,PfTRF was enriched at seven additional, intra-chromosomal sites and called in the PfTRF-HA ChIP-seq only. Plasmodium falciparum 3D7 parasites were generated with -GFP or -3xHA C-terminal tagged TRF (PF3D7_1209300). Nuclei were isolated from formaldehyde cross-linked schizont-stage transgenic parasites and used to prepare chromatin. Chromatin immunoprecipitations were performed using mouse anti-GFP (Roche Diagnostics, #11814460001) or rat anti-HA 3F10 (Roche Diagnostics, #12158167001). Sequencing libraries were prepared according to a Plasmodium-optimized library preparation procedure including KAPA polymerase-mediated PCR amplification.

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