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SRX17444018: GSM6544430: salivary gland sporozoitess_RNA-seq_experiment-2; Plasmodium berghei; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 71.2M spots, 5.4G bases, 1.9Gb downloads

External Id: GSM6544430_r1
Submitted by: mie university
Study: Genome-wide investigation of transcriptional regulation in malaria sporozoite [RNA-Seq]
show Abstracthide Abstract
Sporozoite is the stage in which malaria parasites initially infect the vertebrate host. Elucidation of gene regulation in this stage will promote the investigation of mechanisms of liver infection by this parasite and contribute to development of strategies for preventing the malaria transmission. AP2-Sp is a transcription factor essential for formation of sporozoites or sporogony, which take place in oocysts on the midgut of infected mosquitoes. To understand the role of this transcription factor in the transcriptional regulatory system of this stage we performed ChIP-seq analysis using whole mosquito midguts containing late oocysts as start materials and explore its target genes genome-widely. Target genes were composed of 640 genes, which encompassed various functional categories and were contained genes involved in distinct processes parasites pass through in this stage, from sporogony to development into the liver stage. Furthermore, RNA-seq analysis showed that these genes constituted majority of the genes highly expressed in in this stage. These results suggested that this TF determines basal pattern of gene expression of this stage by targeting a broad range of genes directly. Overall design: Plasmodium berghei transcriptomes were analyzed in oocyst/oocyst sporozoites and salivary gland sporozoites.
Sample: salivary gland sporozoitess_RNA-seq_experiment-2
SAMN30685714 • SRS14998057 • All experiments • All runs
Library:
Name: GSM6544430
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: Dissected midguts were soaked in RNA Later solution until finishing the dissection. RNA extraction was performed using Isogen 2 (Nippon gene) according to the manufacturer's protocol. Dissected midguts were lysed in lysis solution in the kit using Tissuelyser system (Quiagen). Total RNA was extracted using the ISOGEN II (NIPPON GENE, Japan) according to the manufacturer's protocols. Libraries were constructed from total RNA using KAPA mRNA Hyperprep kit (KAPA Biosystems), and sequencing was performed with Illumina NEXTseq sequence (Single read - illumina NextSeq 500),
Runs: 1 run, 71.2M spots, 5.4G bases, 1.9Gb
Run# of Spots# of BasesSizePublished
SRR2144005671,178,9295.4G1.9Gb2022-11-05

ID:
24274576

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