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SRX19634454: GSM7091733: Arabidopsis, Wt Col; Arabidopsis thaliana; OTHER
1 ILLUMINA (Illumina MiSeq) run: 1.5M spots, 465.9M bases, 283.3Mb downloads

External Id: GSM7091733_r1
Submitted by: Donald Danforth Plant Science Center
Study: Targeted site integration in plants using a transposon system [insertion-seq]
show Abstracthide Abstract
Genome editing tools with high precision are key to develop improved crops but current technologies to place new DNA into specific locations in plant genomes are low frequency and error-prone. Transposable elements (TEs) evolved to insert their DNA seamlessly into genomes, albeit in a quasi-random pattern. We developed a genome engineering tool that controls the TE insertion site and subsequently the delivery of any cargo attached to this TE. Using our tool, we demonstrated sequence-specific targeted delivery (guided by the CRISPR gRNA) of enhancers, an open reading frame and gene expression cassette into the genome of the model plant Arabidopsis, and we translated this technology to the crop soybean. We have engineered a 'junk' TE into a useful and accessible toolkit that enables the sequence-specific targeting of custom DNA into plant genomes. Overall design: Insertion-Seq was performed to detect genome-wide insertion sites of the transposable element mPing in various transgenic lines of both Arabidopsis and soybean. Custom libraries were constructed using an adapted HtStuf protocol (PMID: 33228280) with modifications as mentioned below.
Sample: Arabidopsis, Wt Col
SAMN33714553 • SRS17003624 • All experiments • All runs
Library:
Name: GSM7091733
Instrument: Illumina MiSeq
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: SINGLE
Construction protocol: High molecular weight DNA was isolated from fresh Arabidopsis seedlings and Soybean leaf tissue using the NucleoBond HMW DNA kit (Takara), and digested by restriction enzymes XbaⅠ and AluⅠ. Fragmented DNAs ranging from ~450bp to ~2kb were purified from agarose gels, A-tailed by Klenow Fragment (3'-5' exo-; NEB), and ligated to the pGEM T- Easy vector (Promega). 1 µL of this ligation product was used as a template for primary PCR, followed by secondary PCR using nested primers. mPing specific primers were used with the pGEM T- Easy vector primers for primary and secondary PCRs. Barcoded sequencing adapters were added to the amplicons through their inclusion in the PCR primers. The sequencing library for soybean was constructed similarly, except that the genomic DNA was isolated from leaf tissue and digested by XbaⅠ, PmlⅠ, and AluⅠ. After passing quality controls, libraries were run on a MiSeq (Illumina) with V2 output (1X300)
Runs: 1 run, 1.5M spots, 465.9M bases, 283.3Mb
Run# of Spots# of BasesSizePublished
SRR238025761,547,851465.9M283.3Mb2024-05-04

ID:
26932309

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