Multiple Niche Compartments Orchestrate Stepwise Stem Cell Lineage Differentiation
Source: NCBI BioProject (ID PRJNA601761)

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Project name: Multiple Niche Compartments Orchestrate Stepwise Stem Cell Lineage Differentiation
Description: The niche controls stem cell self-renewal and progenitor differentiation for maintaining adult tissue homeostasis in various organisms. However, it remains unclear if the niche is compartmentalized to control stem cell self-renewal and stepwise progeny differentiation. In the Drosophila ovary, inner germarial sheath (IGS) cells form a niche for controlling germline stem cell (GSC) progeny differentiation. In this study, we have identified four IGS subpopulations, which form linearly arranged niche compartments for controlling GSC maintenance and multi-step progeny differentiation. Single-cell analysis of the adult ovary has identified four IGS subpopulations (IGS1-4), which identities and cellular locations have been further confirmed by fluorescent in situ hybridization. IGS1 and IGS2 physically interact with GSCs and mitotic cysts to control GSC maintenance and cyst formation, respectively, whereas IGS3 and IGS4 physically interact with 16-cell cysts to regulate meiosis and oocyte development. Finally, one follicle cell progenitor population has also been transcriptionally defined for facilitating future studies on follicle stem cell regulation. Therefore, this study has structurally revealed that the niche is organized into multiple compartments for orchestrating stepwise adult stem cell development, and has also provided useful resources and tools for further functional characterization of the niche in the future.Overall design: Sort live single GFP positive cells from GMR71E07-GAL4>UAS-GFP, GMR25A11-GAL4>UAS-GFP or GMR31C09-GAL4>UAS-GFP ovaries via Fluorescence-activated cell sorting (FACS). Then these cells were subjected for scRNA-seq according to Single Cell 3' Reagent kits. v2 User Guide Rev D (10X Genomics).
Data type: Transcriptome or Gene expression
Sample scope: Multiisolate
Relevance: ModelOrganism
Organization: Computational Biology, Stowers Institute for Medical Research
Literatures
  1. PMID: 33357404
Last updated: 2020-01-16
Statistics: 3 samples; 3 experiments; 3 runs