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Exogenous delta-crystallin gene expression as probe for differentiation of teratocarcinoma stem cells.

作者信息

Goto K, Hayashi S, Shirayoshi Y, Takeichi M, Kondoh H

机构信息

Department of Biophysics, Faculty of Science, Kyoto University, Japan.

出版信息

Cell Differ. 1988 Jul;24(2):139-47. doi: 10.1016/0045-6039(88)90065-6.

DOI:10.1016/0045-6039(88)90065-6
PMID:3208283
Abstract

We developed an experimental system in which differentiation of teratocarcinoma stem cell is probed by expression of stably introduced exogenous genes. We used chicken delta-crystallin gene (delta gene) and its derivative (Mo delta gene) driven by long terminal repeat (LTR) promoter of Moloney murine leukemia virus (Mo-MuLV). Neither of the genes was expressed in the undifferentiated condition. Differentiation to primitive endoderm induced by retinoic acid (RA) led to expression of delta but not Mo delta, while differentiation to more advanced endodermal cells by RA plus dibutyryl cAMP elicited Mo delta expression in addition to delta. These results are interpreted as a consequence of differential activation/suppression of gene expression through enhancer elements associated with the genes.

摘要

相似文献

1
Exogenous delta-crystallin gene expression as probe for differentiation of teratocarcinoma stem cells.
Cell Differ. 1988 Jul;24(2):139-47. doi: 10.1016/0045-6039(88)90065-6.
2
Differentiation-dependent expression of the chicken delta-crystallin gene introduced into mouse teratocarcinoma stem cells.
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In Vitro Cell Dev Biol. 1991 Jul;27A(7):557-61. doi: 10.1007/BF02631286.