U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX22108368: GSM7844532: NL4.3 CEMM7 n=2 15dpi; Human immunodeficiency virus 1; OTHER
1 ILLUMINA (NextSeq 2000) run: 13M spots, 1.6G bases, 499.6Mb downloads

External Id: GSM7844532_r1
Submitted by: Institute of Molecular Virology, Ulm University Medical Center
Study: Replication-competent HIV-1 gRNA Constructs for CRISPR/Cas9-based Discovery of Antiviral Factors
show Abstracthide Abstract
Innate cellular defense mechanisms and viral countermeasures govern the outcome of pathogen exposure but the complex virus-host interplay remains poorly understood. Here, we developed a virus-guided technology platform where the pathogen itself reveals its cellular opponents. To accomplish this, we engineered replication-competent HIV-1 expressing single guide RNAs (sgRNAs) targeting potential antiviral genes in Cas9 expressing CD4+ T cells. Screening of HIV-1 constructs targeting >500 potential antiviral genes revealed that sgRNAs against GRN, CIITA, EHMT2, CEACAM3, CC2D1B, RHOA and HMOX1 provide significant advantages for viral replication. We verified that GRN and CIITA inhibit HIV-1 in primary CD4+ T cells by reducing viral transcription. Lack of the accessory nef gene increased selection for sgRNAs targeting SERINC5 and IFI16. Functional analyses demonstrated that Nef counteracts the inhibitory effects of IFI16. Altogether, we established a highly versatile, effective and robust approach that forces HIV-1 to reveal its cellular opponents. Overall design: RNA from virus was reverse transcribed and a cassette containing a sgRNA was amplified to sequence the sgRNA
Sample: NL4.3 CEMM7 n=2 15dpi
SAMN37851395 • SRS19173251 • All experiments • All runs
Library:
Name: GSM7844532
Instrument: NextSeq 2000
Strategy: OTHER
Source: OTHER
Selection: other
Layout: PAIRED
Construction protocol: Total RNA was isolated using the Viral RNA Mini Kit (Qiagen) according to the manufacturer's instructions. cDNA reactions were performed according to the manufacturer's instructions of the PrimeScript™ RT Reagent Kit (Takara) using primers specifically targeting the U6 and scaffold region (forward primer 5´-CCGACTCGGTGCCACTTTTT-3´, reverse primer 5´-CGTGACGTAGAAAGTAATAATTT-CTTGGG-3´). cDNA reactions were purified using the Monarch PCR Purification Kit (NEB) and eluted in 10µl elution buffer. The gRNA cassette was amplified using the NEBNext® High-Fidelity 2X PCR Master Mix and primers including Illumina adaptors and 8nt barcodes to allow Next Generation Sequencing (NGS) analysis. PCR reactions were purified using the Monarch PCR Purification Kit (NEB) and eluted in 10µl elution buffer.
Runs: 1 run, 13M spots, 1.6G bases, 499.6Mb
Run# of Spots# of BasesSizePublished
SRR2640266113,040,1491.6G499.6Mb2024-04-15

ID:
30040230

Supplemental Content

Search details

See more...

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...