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Early lineage segregation of multipotent embryonic mammary gland progenitors

ABSTRACT: Early lineage segregation of multipotent embryonic mammary gland progenitors

PROVIDER: PRJNA431774 | ENA |

REPOSITORIES: ENA

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			Action	DRS
	SRR6514400_1.fastq.gz	Fastqsanger.gz
	SRR6514400_2.fastq.gz	Fastqsanger.gz
	SRR6514401_1.fastq.gz	Fastqsanger.gz
	SRR6514401_2.fastq.gz	Fastqsanger.gz
	SRR6514402_1.fastq.gz	Fastqsanger.gz

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Early lineage segregation of multipotent embryonic mammary gland progenitors [expression]

Project description:Early lineage segregation of multipotent embryonic mammary gland progenitors [expression]

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Early lineage segregation of multipotent embryonic mammary gland progenitors [RNA-seq I]

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Early lineage segregation of multipotent embryonic mammary gland progenitors [RNA-Seq II]

Project description:We report single cell RNA-seq data that reveals that Embryonic Multipotent Progenitors (EMPs) in the mammary gland express a unique hybrid basal and luminal signature associated with the different adult lineages.

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Early lineage segregation of multipotent embryonic mammary gland progenitors [expression]

Project description:The mammary gland (MG) is composed of basal cells (BCs) and luminal cells (LCs). While it is generally believed that MG arises from embryonic multipotent progenitors (EMPs), it remains unclear when lineage restriction occurs and what are the mechanisms responsible for the switch from multipotency to unipotency during MG morphogenesis. Here, we performed multicolor lineage tracing and assessed the fate of single embryonic progenitors during mouse MG development. We demonstrated the existence of a developmental switch from multipotency to unipotency during embryonic MG development. Molecular profiling and single cell RNA-seq revealed the hybrid gene expression of EMPs, and the gene trajectory and lineage segregation occurring during MG development. In situ characterization showed that one of the earliest signs of lineage segregation consists in the restricted expression of p63 in the future BCs. Sustained p63 expression during MG development promotes unipotent BC fate in EMPs. Altogether, this study identifies the timing and the mechanisms mediating the switch from multipotency to unipotency during MG development. To understand the molecular mechanisms regulating multipotency during embryonic development, we isolated EMPs by FACS at E14, performed their transcriptional profiling by microarray and compared their transcriptome to adult BCs and LCs

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Early lineage segregation of multipotent embryonic mammary gland progenitors.

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