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Coupling shRNA screens with single-cell RNA-Seq identifies mechanisms regulating senescence during reprogramming

ABSTRACT: Coupling shRNA screens with single-cell RNA-Seq identifies mechanisms regulating senescence during reprogramming

PROVIDER: PRJNA375744 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR5259590.fastq.gz	Fastqsanger.gz
	SRR5259591.fastq.gz	Fastqsanger.gz
	SRR5259592.fastq.gz	Fastqsanger.gz
	SRR5259593.fastq.gz	Fastqsanger.gz
	SRR5259584.fastq.gz	Fastqsanger.gz

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Coupling shRNA screening with single-cell RNA-Seq identifies mechanisms regulating senescence during reprogramming

Project description:Ectopic expression of the transcription factors Oct4, Sox2, Klf4 and c-Myc (OSKM) can reprogram somatic cells into induced pluripotent stem cells (iPSCs). These iPSCs are highly similar to embryonic stem cells and can be used for regenerative medicine, drug screening and disease modelling. Despite recent advances, reprogramming is a slow and inefficient process. This suggests that there are several safeguarding mechanisms to counteract cell fate conversion. Cellular senescence is one of these barriers, which is mediated through activation of the tumour suppressors p53/p21CIP1, p15INK4b and p16INK4a. In this study, we have screened for shRNAs blunting reprogramming-induced senescence. We integrated single-cell RNA sequencing (scRNA-Seq) with shRNA screening to investigate the mechanism of action of the identified candidates.

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Coupling shRNA screens with single-cell RNA-Seq identifies mechanisms regulating senescence during reprogramming

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