Activated transcription via mammalian amino acid response elements does not require enhanced recruitment of the Mediator complex

Nucleic Acids Res. 2008 Oct;36(17):5571-80. doi: 10.1093/nar/gkn538. Epub 2008 Aug 30.

Abstract

It is unclear whether Mediator complex in yeast is necessary for all RNA polymerase II (Pol II) transcription or if it is limited to genes activated by environmental stress. In mammals, amino acid limitation induces SNAT2 transcription through ATF4 binding at an amino acid response element. ATF4 is the functional counterpart to the yeast amino acid-dependent regulator GCN4 and GCN4 recruits Mediator during transcriptional activation. Consistent with enhanced SNAT2 transcription activity, the present data demonstrate that amino acid limitation increased SNAT2 promoter association of the general transcription factors that make up the preinitiation complex, including Pol II, but there was no increase in Mediator recruitment. Furthermore, siRNA knockdown of eight Mediator subunits caused no significant decrease in SNAT2 transcription. The estrogen-dependent pS2 gene was used as a positive control for both the ChIP and the siRNA approaches and the data demonstrated the requirement for Mediator recruitment. These results document that activation of the SNAT2 gene by the mammalian amino acid response pathway occurs independently of enhanced Mediator recruitment.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Transport System A / genetics*
  • Amino Acids / metabolism*
  • Cell Line, Tumor
  • Histones / metabolism
  • Humans
  • Protein Subunits / antagonists & inhibitors
  • Protein Subunits / genetics
  • RNA Interference
  • Response Elements*
  • Transcription Factors, General / antagonists & inhibitors
  • Transcription Factors, General / genetics
  • Transcription Factors, General / metabolism*
  • Transcriptional Activation*

Substances

  • Amino Acid Transport System A
  • Amino Acids
  • Histones
  • Protein Subunits
  • SLC38A2 protein, human
  • Transcription Factors, General