Genetic Engineering Publications - GEG Tech top picks
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Efficient CRISPR/Cas9-Based Genome Engineering in Human Pluripotent Stem Cells

Efficient CRISPR/Cas9-Based Genome Engineering in Human Pluripotent Stem Cells | Genetic Engineering Publications - GEG Tech top picks | Scoop.it
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Pioneering experiments to modify the genome of human pluripotent stem cells (hPS cells) utilizing site-specific double-strand break (DSB)-mediated genome engineering tools, including zinc finger nucleases (ZFNs) and transcription activator-like effector nucleases (TALENs), have paved the way to genome engineering in previously recalcitrant systems. However, these methods are technically cumbersome and require significant expertise, which has limited adoption. In this article, the authors describe commonly practiced methods for CRISPR endonuclease genomic editing of hPS cells into cell lines containing genomes altered by insertion/deletion (indel) mutagenesis or insertion of recombinant genomic DNA.



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7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages - Nature Genetics

7q11.23 dosage-dependent dysregulation in human pluripotent stem cells affects transcriptional programs in disease-relevant lineages - Nature Genetics | Genetic Engineering Publications - GEG Tech top picks | Scoop.it
Giuseppe Testa and colleagues report the generation and transcriptional characterization of patient-derived induced pluripotent stem cells (iPSCs) with copy number variants at 7q11.23, which cause syndromes including neurocognitive phenotypes. They find that the dosage of the transcription factor gene GTF2I accounts for 10-20% of the transcriptional dysregulation observed in these cells.
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Low-Dose Irradiation Enhances Gene Targeting in Human Pluripotent Stem Cells

Low-Dose Irradiation Enhances Gene Targeting in Human Pluripotent Stem Cells | Genetic Engineering Publications - GEG Tech top picks | Scoop.it
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Here, the scientists showed that limited low-dose irradiation (LDI) using either γ-ray or x-ray exposure (0.4 Gy) significantly enhanced HR frequency, possibly through induction of DNA repair/recombination machinery including ataxia-telangiectasia mutated, histone H2A.X and RAD51 proteins. LDI could also increase HR efficiency by more than 30-fold when combined with the targeting tools zinc finger nucleases, transcription activator-like effector nucleases, and clustered regularly interspaced short palindromic repeats.


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