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Mitogens stimulate the rapid nuclear to cytosolic translocation of tristetraprolin, a potential zinc-finger transcription factor.

Publication ,  Journal Article
Taylor, GA; Thompson, MJ; Lai, WS; Blackshear, PJ
Published in: Mol Endocrinol
February 1996

Tristetraprolin (TTP) is the prototype of a group of potential transcription factors that contain two or more unusual CCCH zinc fingers. TTP is encoded by the immediate-early response gene Zfp-36, which is rapidly induced in fibroblasts in response to insulin and other growth factors. Indirect evidence suggests that TTP might function as an inhibitory transcription factor. The present studies evaluated the effect of mitogens on the subcellular localization of TTP using Western blotting of cellular nuclear and cytosolic fractions. In NIH/3T3 mouse fibroblasts that constitutively express TTP, 70% of the protein was located in the nucleus of quiescent, serum-deprived cells. Immunoreactive TTP began to increase in the cytosolic compartment within 1 min of serum stimulation of the cells; this increase in cytosolic protein was essentially complete within 5 min of serum stimulation (81% of total) and was accompanied by a commensurate decrease in nuclear TTP. This translocation was complete well before the increase in TTP synthesis that occurred after serum stimulation. Similar experiments in cells expressing a mutant TTP, in which the major mitogen-activated protein kinase site (serine 220) had been mutated to alanine, revealed normal nuclear to cytosolic translocation after serum stimulation, indicating that phosphorylation of this site is not necessary for this translocation to occur. These results suggest that TTP is rapidly modified in response to mitogens so that it is rapidly released from the nucleus to the cytosol, or that proteins retaining TTP in the nucleus are modified to release it into the cytosol. Thus, TTP's proposed function as a transcription factor, possibly an inhibitory one, may be regulated in cells in part by a novel mechanism, i.e. that of rapid, mitogen-stimulated translocation out of the cellular nucleus.

Duke Scholars

Published In

Mol Endocrinol

DOI

ISSN

0888-8809

Publication Date

February 1996

Volume

10

Issue

2

Start / End Page

140 / 146

Location

United States

Related Subject Headings

  • Zinc Fingers
  • Tristetraprolin
  • Transcription Factors
  • Proteins
  • Molecular Sequence Data
  • Mitogens
  • Mice
  • Metallothionein
  • Immediate-Early Proteins
  • Genes, Immediate-Early
 

Citation

APA
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MLA
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Taylor, G. A., Thompson, M. J., Lai, W. S., & Blackshear, P. J. (1996). Mitogens stimulate the rapid nuclear to cytosolic translocation of tristetraprolin, a potential zinc-finger transcription factor. Mol Endocrinol, 10(2), 140–146. https://doi.org/10.1210/mend.10.2.8825554
Taylor, G. A., M. J. Thompson, W. S. Lai, and P. J. Blackshear. “Mitogens stimulate the rapid nuclear to cytosolic translocation of tristetraprolin, a potential zinc-finger transcription factor.Mol Endocrinol 10, no. 2 (February 1996): 140–46. https://doi.org/10.1210/mend.10.2.8825554.
Taylor GA, Thompson MJ, Lai WS, Blackshear PJ. Mitogens stimulate the rapid nuclear to cytosolic translocation of tristetraprolin, a potential zinc-finger transcription factor. Mol Endocrinol. 1996 Feb;10(2):140–6.
Taylor, G. A., et al. “Mitogens stimulate the rapid nuclear to cytosolic translocation of tristetraprolin, a potential zinc-finger transcription factor.Mol Endocrinol, vol. 10, no. 2, Feb. 1996, pp. 140–46. Pubmed, doi:10.1210/mend.10.2.8825554.
Taylor GA, Thompson MJ, Lai WS, Blackshear PJ. Mitogens stimulate the rapid nuclear to cytosolic translocation of tristetraprolin, a potential zinc-finger transcription factor. Mol Endocrinol. 1996 Feb;10(2):140–146.

Published In

Mol Endocrinol

DOI

ISSN

0888-8809

Publication Date

February 1996

Volume

10

Issue

2

Start / End Page

140 / 146

Location

United States

Related Subject Headings

  • Zinc Fingers
  • Tristetraprolin
  • Transcription Factors
  • Proteins
  • Molecular Sequence Data
  • Mitogens
  • Mice
  • Metallothionein
  • Immediate-Early Proteins
  • Genes, Immediate-Early