N‐myc and c‐src genes are differentially regulated in PCC7 embryonal carcinoma cells undergoing neuronal differentiation

Thomas Sejersen, Håkan Björklund, Janos Sümegi, Nils R. Ringertz

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

We examined the expression of N‐myc, c‐myc, and c‐src in four embryonic carcinoma (EC) cell lines during different states of cell growth and following induction of in vitro differentiation. N‐myc mRNA was detected in undifferentiated cells of four EC cell lines (PCC7, PCC3, PCC4, F9) neither of which showed N‐myc gene amplification. No N‐myc transcripts could be detected in mRNA prepared from a murine neuroblastoma cell line and from a murine fibroblast line. The level of N‐myc mRNA decreased by 85% when PCC7 EC cells were induced by retinoic acid and cAMP treatment to form nerve‐like cells. Six days after induction, the PCC7 cells changed into aggregates of neurofilament positive cells with massive neurite outgrowths. At this stage DNA replication had been reduced by more than 95%. The decreased N‐myc expression in induced PCC7 cells was parallelled by 300–500% increase in c‐src expression. Slowing of cell multiplication by serum starvation, on the other hand, did not affect the level of N‐myc or c‐src mRNA levels in PCC7 cells. C‐myc was expressed in all EC lines except PCC7, which surprisingly did not express c‐myc even at an exponential rate of proliferation. Chemical induction of F9 EC cells to form visceral endoderm or parietal endoderm resulted in markedly reduced (85%) levels of N‐myc transcripts. A similar decline in c‐myc expression was found in differentiated F9 cells. No c‐src transcripts were detected in proliferating or differentiated F9 cells. These results suggest that N‐myc may be expressed not only in neural development, but also in very early, undetermined embryonic cells. The activation of c‐src expression when PCC7 EC cells differentiate into nerve‐like cells shows that the pattern of proto‐oncogene expression may change during a differentiation process, some proto‐oncogenes increasing, others decreasing their representation in the mRNA pool.

Original languageEnglish (US)
Pages (from-to)274-280
Number of pages7
JournalJournal of Cellular Physiology
Volume127
Issue number2
DOIs
StatePublished - May 1986

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Embryonal Carcinoma Stem Cells
Genes
Cells
Messenger RNA
Carcinoma
Cell growth
Fibroblasts
Tretinoin
Endoderm
Chemical activation
Cell Line
Embryonic Induction
DNA
Intermediate Filaments
Gene Amplification
Starvation
DNA Replication
Neuroblastoma

ASJC Scopus subject areas

  • Physiology
  • Clinical Biochemistry
  • Cell Biology

Cite this

N‐myc and c‐src genes are differentially regulated in PCC7 embryonal carcinoma cells undergoing neuronal differentiation. / Sejersen, Thomas; Björklund, Håkan; Sümegi, Janos; Ringertz, Nils R.

In: Journal of Cellular Physiology, Vol. 127, No. 2, 05.1986, p. 274-280.

Research output: Contribution to journalArticle

Sejersen, Thomas ; Björklund, Håkan ; Sümegi, Janos ; Ringertz, Nils R. / N‐myc and c‐src genes are differentially regulated in PCC7 embryonal carcinoma cells undergoing neuronal differentiation. In: Journal of Cellular Physiology. 1986 ; Vol. 127, No. 2. pp. 274-280.
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abstract = "We examined the expression of N‐myc, c‐myc, and c‐src in four embryonic carcinoma (EC) cell lines during different states of cell growth and following induction of in vitro differentiation. N‐myc mRNA was detected in undifferentiated cells of four EC cell lines (PCC7, PCC3, PCC4, F9) neither of which showed N‐myc gene amplification. No N‐myc transcripts could be detected in mRNA prepared from a murine neuroblastoma cell line and from a murine fibroblast line. The level of N‐myc mRNA decreased by 85{\%} when PCC7 EC cells were induced by retinoic acid and cAMP treatment to form nerve‐like cells. Six days after induction, the PCC7 cells changed into aggregates of neurofilament positive cells with massive neurite outgrowths. At this stage DNA replication had been reduced by more than 95{\%}. The decreased N‐myc expression in induced PCC7 cells was parallelled by 300–500{\%} increase in c‐src expression. Slowing of cell multiplication by serum starvation, on the other hand, did not affect the level of N‐myc or c‐src mRNA levels in PCC7 cells. C‐myc was expressed in all EC lines except PCC7, which surprisingly did not express c‐myc even at an exponential rate of proliferation. Chemical induction of F9 EC cells to form visceral endoderm or parietal endoderm resulted in markedly reduced (85{\%}) levels of N‐myc transcripts. A similar decline in c‐myc expression was found in differentiated F9 cells. No c‐src transcripts were detected in proliferating or differentiated F9 cells. These results suggest that N‐myc may be expressed not only in neural development, but also in very early, undetermined embryonic cells. The activation of c‐src expression when PCC7 EC cells differentiate into nerve‐like cells shows that the pattern of proto‐oncogene expression may change during a differentiation process, some proto‐oncogenes increasing, others decreasing their representation in the mRNA pool.",
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