Unknown,Transcriptomics,Genomics,Proteomics

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RNA-sequencing analysis of NGN3-GFP positive and negative cells purified from differentiating human embryonic stem cells


ABSTRACT: NGN3-eGFP could be used to mark endocrine progenitor cells and their progeny in differentiating hESCs, suggesting that profiling analysis of NGN3-eGFP+ cells could lead to the discovery of novel gene participation. Six batches of NGN3-eGFP+ and NGN3-eGFP -cells purified by FACS from a reporter hES cell line cell cultures at stage 4 were pooled together, respectively. RNA-seq-based analysis of the two cell fractions identified a total of 3976 differentially expressed genes (P-value<0.05; Fold >2), of which 72% are enriched in NGN3-GFP+ cells. As expected, all the genes expressed in pancreatic progenitor cells are enriched in NGN3-eGFP-cells; while all endocrine-associated genes are enriched in NGN3-eGFP+ cells. Among the 3976 genes, 195 have potential transcriptional factor activity and 453 are potential non-coding RNA genes, most of which have not been well investigated in pancreatic endocrine cells. The gene ontology term M-bM-^@M-^Xintegral to membraneM-bM-^@M-^Y GO: 0016021 identified 1003 differentially expressed genes that encoded ion channels, adhesion molecules and transporters. NGN3-eGFP Postive and negtive cells were purified at stage 4 and subjected to RNA-sequncing

ORGANISM(S): Homo sapiens

SUBMITTER: ilmen zhang 

PROVIDER: E-GEOD-54879 | biostudies-arrayexpress |

REPOSITORIES: biostudies-arrayexpress

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Publications

Systematically labeling developmental stage-specific genes for the study of pancreatic β-cell differentiation from human embryonic stem cells.

Liu Haisong H   Yang Huan H   Zhu Dicong D   Sui Xin X   Li Juan J   Liang Zhen Z   Xu Lei L   Chen Zeyu Z   Yao Anzhi A   Zhang Long L   Zhang Xi X   Yi Xing X   Liu Meng M   Xu Shiqing S   Zhang Wenjian W   Lin Hua H   Xie Lan L   Lou Jinning J   Zhang Yong Y   Xi Jianzhong J   Deng Hongkui H  

Cell research 20140905 10


The applications of human pluripotent stem cell (hPSC)-derived cells in regenerative medicine has encountered a long-standing challenge: how can we efficiently obtain mature cell types from hPSCs? Attempts to address this problem are hindered by the complexity of controlling cell fate commitment and the lack of sufficient developmental knowledge for guiding hPSC differentiation. Here, we developed a systematic strategy to study hPSC differentiation by labeling sequential developmental genes to e  ...[more]

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