Mutually dependent response elements in the cis-regulatory region of the neurotensin/neuromedin N gene integrate environmental stimuli in PC12 cells

Neuron. 1990 May;4(5):783-95. doi: 10.1016/0896-6273(90)90205-t.

Abstract

The expression of the gene encoding the neuroendocrine peptides neurotensin (NT) and neuromedin N is strictly dependent on simultaneous exposure to multiple inducers in PC12 pheochromocytoma cells. NT peptide and NT/N mRNA levels are synergistically induced by combinations of NGF, dexamethasone, activators of adenylate cyclase, and lithium ion. We have used transient transfection assays to delineate the rat NT/N gene sequences necessary for this complex regulation. Progressive deletions of the 5' flanking region revealed that sequences between -216 and +56 are sufficient to confer the full spectrum of responses exhibited by the endogenous gene to a reporter gene. Detailed mutational analysis of this region indicates that it is composed of an array of inducible cis-regulatory sequences, including AP-1, cAMP response, and glucocorticoid response elements. Specific mutation of either the AP-1 site or each of two cAMP response elements indicates that they are functionally interdependent. This array of response elements serves to integrate multiple environmental stimuli into a unified transcriptional response.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adrenal Gland Neoplasms / genetics
  • Adrenal Gland Neoplasms / metabolism
  • Adrenal Gland Neoplasms / pathology
  • Adrenal Gland Neoplasms / physiopathology*
  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Chromosome Mapping
  • Fibroblasts / cytology
  • Fibroblasts / metabolism
  • Fibroblasts / physiology
  • Gene Expression / drug effects
  • Gene Expression / physiology
  • Genes, Regulator / physiology*
  • Molecular Sequence Data
  • Neurotensin / genetics*
  • Neurotensin / metabolism
  • Neurotensin / physiology
  • Peptide Fragments / genetics*
  • Peptide Fragments / metabolism
  • Peptide Fragments / physiology
  • Phenotype
  • Pheochromocytoma / genetics
  • Pheochromocytoma / metabolism
  • Pheochromocytoma / pathology
  • Pituitary Gland / cytology
  • Pituitary Gland / metabolism
  • Pituitary Gland / physiology
  • Promoter Regions, Genetic / physiology
  • Rats
  • Tumor Cells, Cultured / pathology*

Substances

  • Peptide Fragments
  • neuromedin N
  • Neurotensin