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Roles of Sall4 in the generation of pluripotent stem cells from blastocysts and fibroblasts.

http://www.ncbi.nlm.nih.gov/pubmed/19476507

Pluripotency of embryonic stem (ES) cells is maintained by a network consisting of multiple transcription factors, including Oct3/4, Sox2, Nanog, Klf4 and Sall4. Among these factors, the forced expressions of Oct3/4, Sox2 and Klf4 are sufficient to reprogram fibroblasts into induced pluripotent stem (iPS) cells. The current study analyzed the role of Sall4 during the generation of ES cells and iPS cells. The mouse Sall4 gene was deleted by homologous recombination. Sall4-null embryos died shortly after implantation, as has been reported. ES-like cell lines can be established from Sall4-null blastocysts, albeit with a lower efficiency and a slower time course. The knockdown of Sall4 significantly decreased the efficiency of iPS cell generation from mouse fibroblasts. Furthermore, retroviral transduction of Sall4 significantly increased the efficiency of iPS cell generation in mouse and some human fibroblast lines. These results demonstrated that Sall4 plays positive roles in the generation of pluripotent stem cells from blastocysts and fibroblasts.

Pubmed ID: 19476507 RIS Download

Mesh terms: Animals | Blastocyst | Cell Differentiation | DNA-Binding Proteins | Embryonic Stem Cells | Fibroblasts | Gene Expression Regulation, Developmental | Humans | Mice | Pluripotent Stem Cells | Transcription Factors

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Mouse Genome Informatics (Data, Gene Annotation)

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