Mouse ChIP-Seq

Mouse ChIP-Seq

The mouse is the most used animal model in the literature. The vast majority of the literature uses various strains of mice. This is because mice are 99% genetically similar to humans. Also, mice are small, inexpensive, have a diverse diet, and reproduce quickly. Researchers can study several generations of their offspring simultaneously in a relatively short period of time. Also, the physiology and genetics of mice have been extensively studied and can be easily compared to humans.

More importantly, techniques used to study genetics and specific gene functions, such as transgenic approaches, have been developed in mice for decades. Mouse models of many human diseases have been established to facilitate the study of pathogenesis and to assess the effects and toxicity of various drug candidates. Mouse genomes have been sequenced, and ChIP-seq techniques are often applied to mouse models to decode the mystery of protein-DNA binding.

Lifeasible, a world-renowned plant, and animal biotechnology company, has built a cutting-edge sequencing technology platform with state-of-the-art sequencing instruments and can spare no effort to provide you with customized mouse ChIP-seq services. Our service is designed to help you detect DNA segments that interact with histones, transcription factors, etc., on a genome-wide scale.

Mouse ChIP-seq

Our Mouse ChIP-Seq Service Content

Our mouse ChIP-seq technology service is universal, easy to use, has high throughput and high quality and is capable of targeting various organ tissues and cells in mouse models for specific purposes.

Correlation studies of transcription factors in mouse ectodermal stem cells

Through an efficient ChIP analysis procedure, we investigated the chromosomal regions of five major transcription factors (ZIC2, OTX2, SOX2, POU5F1, and POU3F1) in mouse ectodermal stem cells, demonstrating their involvement in EpiSC maintenance and somatic cell development processes.

Figure 1. ChIP-seq data of five major transposable elements.Figure 1. ChIP-seq data of five major transposable elements. (Matsuda, K, et al. 2017)

Exploration of dynamic chromatin mapping of mouse fetal development

Through multiple chromatin immunoprecipitation and ChIP-seq, we annotated chromatin states during mouse fetal development and mapped chromatin dynamics view to describe the relationship between chromatin states and accessibility during developmental gene regulation. This mouse model of ChIP-seq can help scientists in the study of mammalian fetal developmental processes.

Figure 2. ChIP–seq data summary. (Gorkin, D. U, et al. 2020)Figure 2. ChIP–seq data summary. (Gorkin, D. U, et al. 2020)

Detection of transcription factor binding sites (TFBS) in mouse

TFBS are critical for gene regulation, yet most TFBS remain unknown. To discover new TFBS, we sequenced mice using ChIP-seq technology and then analyzed the sequencing data to infer new TFBS.

Figure 3. Flow chart of the detection of TFBS by ChIP-seq technology. (Yu, C. P, et al. 2021)Figure 3. Flow chart of the detection of TFBS by ChIP-seq technology. (Yu, C. P, et al. 2021)

Exploration of disease mechanisms based on ChIP-seq in mouse

By performing ChIP-seq on mouse intestinal precursor cells, we revealed new potential genes RABGGTB, BRD3, TGFB1, HRAS, and GRB2 that play a role in developing the enteric nervous system and congenital megacolonosis.

Technical Route of Mouse ChIP-Seq

Technical route of mouse ChIP-seq. - Lifeasible

Sample Requirements

  • Sample type: DNA sample, cell, or tissue.
  • Total sample volume: ≥ 10 ng of ChIPed DNA or ≥ 107 of cell volume or 2 g of tissue.
  • DNA samples: OD260/280 values should be between 1.8 and 2.0.
  • Preservation solvent for DNA: in H2O or TE (pH 8.0).
  • Sample transport: choose the fastest transport method to avoid sample degradation. Please seal the tube mouth with parafilm during transport to prevent contamination.

It is recommended to provide two sample preparations, if possible, to ensure the quality and continuity of the experiment.

Bioinformatics Analysis Content

  • Sequencing data quality assessment (QC)
  • Comparison to reference genomes and data statistics
  • Genome distribution statistics
  • Peak calling analysis
  • Peak cis-regulatory element distribution
  • Peak region gene annotation
  • Peak difference analysis
  • Peak-associated gene GO annotation
  • KEGG annotation of Peak-related genes
  • Motif analysis of transcription binding sites (for transcription factors only)

Lifeasible's animal-oriented sequencing technology platform can provide you with various mouse ChIP-seq solutions to help you perform functional enrichment analysis, predict the function of specific proteins, map histone chromosome binding, and detect episomal modifications of DNA. For questions, inquiries, or collaboration, please feel free to contact us.

References

  1. Matsuda, K.; et al. (2017). ChIP-seq analysis of genomic binding regions of five major transcription factors highlights a central role for ZIC2 in the mouse epiblast stem cell gene regulatory network. Development (Cambridge, England), 144(11), 1948–1958.
  2. Gorkin, D. U.; et al. (2020). An atlas of dynamic chromatin landscapes in mouse fetal development. Nature, 583(7818), 744–751.
  3. Yu, C. P.; et al. (2021). Discovering unknown human and mouse transcription factor binding sites and their characteristics from ChIP-seq data. Proceedings of the National Academy of Sciences of the United States of America, 118(20), e2026754118.
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