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SRX22530758: GSM7900914: HA-CUT&Tag of Dek-KO E14TG2a cells complemented with HA-Dek-LRM_deletion repeat 2; Mus musculus; OTHER
1 ILLUMINA (Illumina HiSeq 2000) run: 47.9M spots, 14.4G bases, 4.5Gb downloads

External Id: GSM7900914_r1
Submitted by: central south university
Study: Structural basis of the DEK-nucleosome complex and its functional implications
show Abstracthide Abstract
The nuclear factor Dek is notably enriched within chromatin; nevertheless, the precise binding mechanism of Dek to the nucleosome remains elusive. In this study, we employ cryo-electron microscopy (cryo-EM) to elucidate the high-resolution structure of the Dek-Nucleosome Core Particle (NCP) complex. We identify specific domains responsible for DEK interaction with the histone octamer and DNA within the nucleosome. The veracity of these binding domains is confirmed through a series of meticulous biochemical experiments. Subsequently, cellular experiments reveal that Dek lacking nucleosome-binding capacity exhibits a deficiency in chromatin interaction. Remarkably, this impairment induces a shift towards the primitive endoderm fate in mouse embryonic stem cells, underscoring the pivotal role of Dek in determining cell fate through its nucleosomal interactions. Overall design: HA-labeled wild-type DEK and various key domain mutations were overexpressed in DEK-knockout cells. CUT&Tag for HA was employed to assess the impact of mutations on the distribution of Dek on chromatin, while RNA-seq was used to identify transcriptomic changes induced by these mutations in the cells.
Sample: HA-CUT&Tag of Dek-KO E14TG2a cells complemented with HA-Dek-LRM_deletion repeat 2
SAMN38262187 • SRS19541548 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM7900914
Instrument: Illumina HiSeq 2000
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: PAIRED
Construction protocol: The CUT&Tag was performed following the protocol provided by the Hieff NGS® G-Type In-Situ DNA Binding Profiling Library Prep Kit (Yeasen). A total of 50,000 cells were harvested and subjected to two rounds of washing using washing buffer (composed of 20 mM HEPES pH 7.5, 150 mM NaCl, 0.5 mM Spermidine, and 1× Protease inhibitor cocktail). Subsequently, the cells were incubated with activated Concanavalin A coated magnetic beads. To this, 0.5 μg of HA antibody was added and allowed to incubate on a rotating platform at 4 °C for a duration of 16 hours. Following this, 0.5 μL of Goat anti-Rabbit secondary antibody was introduced and incubated for an additional hour. After a thorough washing step, the cells were treated with pA/G-Tn5 transposase at 37°C for 1 hour. Subsequently, DNA extraction was carried out by DNA selection beads Total RNA was harvested using Trizol reagent from 5*10^6 ESCs. To amplify libraries, 16 μL CUT&Tag DNA was mixed with 1 μL of a uniquely barcoded i5, 1 μL a uniquely barcoded i7 primer, using a different barcode for each sample, 7 μL ddH2O, and 25 μL 2× Ultima Amplification Mix, and run the following cycling conditions with lid heat on: 72 °C for 3 min; 95 °C for 30 s; 12 cycles of 95 °C for 10 s, 55 °C for 30 s and 72 °C for 30 s; final extension at 72 °C for 5 min and hold at 4 °C. Post-PCR clean-up was performed by adding 1.2× volume of DNA selection beads (60 μL), and libraries were incubated with beads for 5 min at RT, washed twice gently in 80% ethanol, and eluted in 20 μL EB buffer. RNA libraries were prepared for sequencing using standard
Runs: 1 run, 47.9M spots, 14.4G bases, 4.5Gb
Run# of Spots# of BasesSizePublished
SRR2683480847,941,23314.4G4.5Gb2023-12-31

ID:
30522764

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