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SRX18901426: GSM6911244: RNA_L2C_Ctrl_rep2; Mus musculus; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 8.6M spots, 2.6G bases, 856.5Mb downloads

External Id: GSM6911244_r1
Submitted by: Tsinghua University
Study: Maternal TDP-43 interacts with RNA Pol II and regulates zygotic genome activation
show Abstracthide Abstract
Zygotic genome activation (ZGA) is essential for early embryonic development. However, the regulation of ZGA remains elusive in mammals. Here we report that a maternal factor TDP-43, a nuclear transactive response DNA-binding protein, regulates ZGA through RNA Pol II and is essential for mouse early embryogenesis. Maternal TDP-43 translocates from the cytoplasm into the nucleus at the early two-cell stage when minor to major ZGA transition occurs. Genetic deletion of maternal TDP-43 results in mouse early embryos arrested at late two-cell stage and female infertile. TDP-43 co-occupies with RNA Pol II as large foci in the nucleus and also at the promoters of ZGA genes at the late two-cell stage. Biochemical evidence indicates that TDP-43 binds Polr2a and Cyclin T1. Depletion of maternal TDP-43 caused the loss of Pol II foci and reduced Pol II binding on chromatin at major ZGA genes, accompanied by defective ZGA. Collectively, our results suggest that maternal TDP-43 is critical for mouse early embryonic development, in part through facilitating the correct RNA Pol II configuration and zygotic genome activation. Overall design: RNA-seq experiments were performed in WT and TDP-43 knockout mouse oocytes, one-cell and two-cell embryos.Stacc-seq experiments were applied to WT FGO and embryos with the antibodies against Pol II or TDP43 and to TDP-43 knockout two-cell embryos with the Pol II antibody.
Sample: RNA_L2C_Ctrl_rep2
SAMN32527222 • SRS16330194 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM6911244
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: The oocytes and embryos were collected as Smart-seq2 or Stacc-seq protocols in the paper, and the extraction was amplificated or used for the library directly as in the paper. For RNA-seq, RNA libraries for RNA-seq were prepared using a kit of Vazyme (TD502) and performed as the protocol of manufacture. For stacc-seq, Stacc-seq libraries performed according to the previous report.1 μl fully dissolved 5% digitonin was added to Buffer1 (10 mM Tris-HCl pH = 7.4, 150 mM NaCl, 0.5 mM spermidine, 1 × EDTA-free Roche complete protease inhibitor). 0.5 μl PA/G-Tn5 and 0.5 μg TDP-43 or Pol II antibody was added to prepared Buffer1 and incubated at 4℃ for 30 min. Meanwhile, oocytes and embryos were treated gently with Tyrode's solution for removing the zona pellucida, then were put into 200ml low-binding tube contained 6ml prepared Buffer1 and incubate 4℃ for 10 min . Then 35 ml the prepared Buffer1, mixture of PA/G-Tn5, and the antibody and 12.5 ml TTBL were added for cleaving the chromatin around the binding sites and transposing with adaptors. Then the DNA were purified and PCR as the stacc-seq steps in previously reported
Runs: 1 run, 8.6M spots, 2.6G bases, 856.5Mb
Run# of Spots# of BasesSizePublished
SRR229441918,635,2142.6G856.5Mb2023-06-24

ID:
26011279

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