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SRX7635171: GSM4284927: HAP1 + AsCas12a + Optimization Library + 6-thioguanine; Homo sapiens; OTHER
3 ILLUMINA (NextSeq 500) runs: 3.8M spots, 283.9M bases, 99.7Mb downloads

Submitted by: NCBI (GEO)
Study: Genetic interaction mapping and exon-resolution functional genomics with a hybrid Cas9-Cas12a platform
show Abstracthide Abstract
Systematic mapping of genetic interactions and interrogation of the functions of sizeable genomic segments in mammalian cells represent important goals of biomedical research. To advance these goals, we present a CRISPR-based screening system for combinatorial genetic manipulation that employs co-expression of Cas9 and Cas12a nucleases and machine learning-optimized libraries of hybrid Cas9-Cas12a guide RNAs. This system, named CHyMErA (Cas Hybrid for Multiplexed Editing and Screening Applications), outperforms genetic screens using Cas9 or Cas12a editing alone. Application of CHyMErA to the ablation of mammalian paralog gene pairs reveals extensive genetic interactions and uncovers phenotypes normally masked by functional redundancy. Application of CHyMErA in a chemo-genetic interaction screen identifies genes that impact cell growth in response to mTOR pathway inhibition. Moreover, by systematically targeting thousands of alternative splicing events, CHyMErA identifies exons underlying human cell line fitness. CHyMErA thus represents an effective screening approach for genetic interaction mapping and the functional analysis of sizeable genomic regions, such as alternative exons. Overall design: Eight CRISPR screens were performed with four different CHyMErA hybird guide (hg)RNA libraries in human and mouse cell lines. All screens were performed with three biologically independent replicates that were derived from the same library infection and were sequenced at multiple time points. (1) A screen were performed using a human optimization hgRNA library in HAP1 cells and that were subjected to 6-thioguanine and thymidine treatment while non-treated cells were used as controls. (2) A screen were performed using a mouse optimization hgRNA library in CGR8 cells. (3) Screens with a human 2nd generation hgRNA library for single- and dual-gene targeting plus paralog pairs were performed in human HAP1 and RPE1 cells. HAP1 cells were also treated with Torin1 and non-treated cells served as control. (4) A screen with a human exon deletion hgRNA library was performed in RPE1 cells.
Sample: HAP1 + AsCas12a + Optimization Library + 6-thioguanine
SAMN13927455 • SRS6065898 • All experiments • All runs
Organism: Homo sapiens
Library:
Instrument: NextSeq 500
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: Genomic DNA was extracted using the Wizard Genomic DNA Purification Kit (Promega). Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Sequencing libraries were prepared in two PCR steps, the first to enrich guide-RNA regions from the genome, and the second to amplify guide-RNA and attach Illumina TruSeq adapters with i5 and i7 indices. Libraries were prepared according to Illumina's instructions accompanying the DNA Sample Kit (Part# 0801-0303). Briefly, DNA was end-repaired using a combination of T4 DNA polymerase, E. coli DNA Pol I large fragment (Klenow polymerase) and T4 polynucleotide kinase. The blunt, phosphorylated ends were treated with Klenow fragment (32 to 52 exo minus) and dATP to yield a protruding 3- 'A' base for ligation of Illumina's adapters which have a single 'T' base overhang at the 3' end. After adapter ligation DNA was PCR amplified with Illumina primers for 15 cycles and library fragments of ~250 bp (insert plus adaptor and PCR primer sequences) were band isolated from an agarose gel. The purified DNA was captured on an Illumina flow cell for cluster generation. Libraries were sequenced on the Genome Analyzer following the manufacturer's protocols.
Experiment attributes:
GEO Accession: GSM4284927
Links:
Runs: 3 runs, 3.8M spots, 283.9M bases, 99.7Mb
Run# of Spots# of BasesSizePublished
SRR109695991,287,91895.3M33.4Mb2020-02-04
SRR109696001,161,25885.9M30.1Mb2020-02-04
SRR109696011,387,510102.7M36.3Mb2020-02-04

ID:
9964675

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