Derivation and maintenance of mouse haploid embryonic stem cells.
Ulrich EllingMichael WoodsJosep V FormentBeiyuan FuFengtang YangBee Ling NgJose R VicenteDavid J AdamsBrendan DoeStephen P JacksonJosef M PenningerGabriel BalmusPublished in: Nature protocols (2019)
Ploidy represents the number of chromosome sets in a cell. Although gametes have a haploid genome (n), most mammalian cells have diploid genomes (2n). The diploid status of most cells correlates with the number of probable alleles for each autosomal gene and makes it difficult to target these genes via mutagenesis techniques. Here, we describe a 7-week protocol for the derivation of mouse haploid embryonic stem cells (hESCs) from female gametes that also outlines how to maintain the cells once derived. We detail additional procedures that can be used with cell lines obtained from the mouse Haplobank, a biobank of >100,000 individual mouse hESC lines with targeted mutations in 16,970 genes. hESCs can spontaneously diploidize and can be maintained in both haploid and diploid states. Mouse hESCs are genomically and karyotypically stable, are innately immortal and isogenic, and can be derived in an array of differentiated cell types; they are thus highly amenable to genetic screens and to defining molecular connectivity pathways.
Keyphrases
- embryonic stem cells
- genome wide
- induced apoptosis
- cell cycle arrest
- single cell
- copy number
- cell therapy
- randomized controlled trial
- high throughput
- oxidative stress
- crispr cas
- gene expression
- white matter
- clinical trial
- high resolution
- endoplasmic reticulum stress
- transcription factor
- mass spectrometry
- drug delivery
- bioinformatics analysis
- bone marrow