Expression of the CRE-BP1 transcriptional regulator binding to the cyclic AMP response element in central nervous system, regenerating liver, and human tumors

Oncogene. 1991 Jun;6(6):1009-14.

Abstract

CRE-BP1 is a transcriptional regulator binding to the cyclic AMP response element (CRE). To understand the role of CRE-BP1 in vivo, we studied the expression of the CRE-BP1 gene in monkey tissues including the central nervous system, in rat regenerating liver, and in human cancer tissues compared with normal tissues. The CRE-BP1 mRNA was detected in all tissues examined, and was fairly abundant in brain. The CRE-BP1 mRNA was expressed in monkey brain tissues with different region specificities. In the hippocampus, frontal lobe, and parietal lobe, the CRE-BP1 mRNA was abundant and two mRNA species 4.0 kb and 3.7 kb in length were expressed. In rat liver, the expression of the CRE-BP1 gene was increased up to 4- to 5-fold of the normal level within 12-24 h after partial hepatectomy. Furthermore, the levels of CRE-BP1 mRNA in some clinical samples of human tumors were apparently higher than that in normal tissues. These results suggest that CRE-BP1 may be important for both the signal transduction in brain and cellular proliferation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Northern
  • Brain / cytology
  • Brain / metabolism
  • Central Nervous System / cytology
  • Central Nervous System / metabolism*
  • Colonic Neoplasms / metabolism*
  • Colonic Neoplasms / pathology
  • Cyclic AMP Response Element-Binding Protein
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • DNA-Binding Proteins / physiology
  • Esophageal Neoplasms / metabolism*
  • Esophageal Neoplasms / pathology
  • Gene Expression
  • Humans
  • Immunohistochemistry
  • Liver / cytology
  • Liver / metabolism*
  • Liver / physiology
  • Macaca fascicularis
  • Male
  • RNA, Messenger / genetics
  • Rats
  • Rats, Inbred Strains
  • Regeneration / physiology
  • Stomach Neoplasms / metabolism*
  • Stomach Neoplasms / pathology
  • Transcription, Genetic / genetics

Substances

  • Cyclic AMP Response Element-Binding Protein
  • DNA-Binding Proteins
  • RNA, Messenger