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A UTF1 -based selection system for stable homogeneously pluripotent human embryonic stem cell cultures
Author(s) -
Shen Mynn Tan,
Siew Tein Wang,
Hannes Hentze,
Peter Dröge
Publication year - 2007
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkm704
Subject(s) - biology , homeobox protein nanog , sox2 , reprogramming , embryonic stem cell , induced pluripotent stem cell , stem cell , microbiology and biotechnology , somatic cell , epiblast , cellular differentiation , kosr , genetics , cell , gene , gastrulation
Undifferentiated transcription factor 1 (UTF1) was identified first in mouse embryonic stem cells and is also expressed in human embryonic and adult stem cells. UTF1 transcription ceases at the onset of differentiation, which clearly distinguishes it from less sensitive pluripotency markers, such as Oct4 or Nanog. We present here two transgenic hESC lines, named ZUN. Each line harbors one copy of the UTF1 promoter/enhancer driving a resistance gene and yielded highly homogeneous cultures under selec- tion pressure, with a larger proportion of Oct4 and Sox2 positive cells. While ZUN cultures, like parental HUES8 cultures, retained the capacity to differenti- ate into tissues of all three germ layers using a SICD mouse teratoma model, they surprisingly exhibited an increased refractoriness to various differentia- tion cues in vitro. Together with its small size of only 2.4 kb for the entire cassette, these features render our selection system a powerful novel tool for many stem cell applications and human somatic cell reprogramming strategies.

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