Feed-back regulation of disabled-2 (Dab2) p96 isoform for GATA-4 during differentiation of F9 cells

Jung Ah Kim, Seong Ho Bae, Young Joon Choi, Kyung Hyun Kim, Sung Soo Park

Research output: Contribution to journalArticle

7 Citations (Scopus)

Abstract

F9 embryonic carcinoma (EC) cells undergo extra-embryonic endodermal (ExE) differentiation in response to retinoic acid (RA) treatment, which induces the expression of two isoforms (p96 and p67) of the adaptor protein, Disabled-2 (Dab2). In the current study, constitutive and ectopic expression of the p96 isoform induced ExE differentiation in F9 EC cells in the absence of RA treatment via the activation of GATA-4 by p96. During the RA-induced differentiation process, Dab2 expression is induced by the GATA factors in a coherent feed-forward loop; on the other hand, we showed that p96 regulates GATA-4 in a positive feed-back manner in this study. Our results indicate that p96 Dab2 plays a key role in the ExE differentiation process.

Original languageEnglish
Pages (from-to)591-598
Number of pages8
JournalBiochemical and Biophysical Research Communications
Volume421
Issue number3
DOIs
Publication statusPublished - 2012 May 11

Fingerprint

Tretinoin
Cell Differentiation
Protein Isoforms
Feedback
GATA Transcription Factors
Carcinoma
Chemical activation
Cells
Proteins

Keywords

  • Disabled-2 (Dab2)
  • Extra-embryonic endoderm (ExE)
  • Feed-back loop
  • GATA-4

ASJC Scopus subject areas

  • Biochemistry
  • Biophysics
  • Cell Biology
  • Molecular Biology

Cite this

Feed-back regulation of disabled-2 (Dab2) p96 isoform for GATA-4 during differentiation of F9 cells. / Kim, Jung Ah; Bae, Seong Ho; Choi, Young Joon; Kim, Kyung Hyun; Park, Sung Soo.

In: Biochemical and Biophysical Research Communications, Vol. 421, No. 3, 11.05.2012, p. 591-598.

Research output: Contribution to journalArticle

Kim, Jung Ah ; Bae, Seong Ho ; Choi, Young Joon ; Kim, Kyung Hyun ; Park, Sung Soo. / Feed-back regulation of disabled-2 (Dab2) p96 isoform for GATA-4 during differentiation of F9 cells. In: Biochemical and Biophysical Research Communications. 2012 ; Vol. 421, No. 3. pp. 591-598.
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