Cloning and characterization of 5'-upstream region of human phospholipase C-beta2 gene

Exp Mol Med. 2001 Jun 30;33(2):76-82. doi: 10.1038/emm.2001.14.

Abstract

5'-upstream region of the phospholipase C-beta2 gene, 810 bp, was cloned and characterized. S1 nuclease mapping and primer extension analyses revealed that a single transcriptional start site locates at 284 nucleotides upstream from the beginning of translation. The 5-upstream region lacks both TATA motif and typical initiator sequence, but retains GC-rich segment. Two putative regulatory regions, a negative region (-636/-588) and a positive region (-98/ -13) were identified in the upstream region of PLC-beta2 gene. We suggest that the transcription of PLC-beta2 may be regulated by binding of regulatory proteins to the negative and/or positive regulatory regions located in the upstream of the gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cells, Cultured
  • Chloramphenicol O-Acetyltransferase / metabolism
  • Cloning, Molecular
  • Conserved Sequence
  • Gene Deletion
  • Isoenzymes / chemistry*
  • Isoenzymes / genetics*
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Phospholipase C beta
  • Promoter Regions, Genetic
  • Protein Binding
  • Single-Strand Specific DNA and RNA Endonucleases / metabolism
  • Transcription, Genetic
  • Transfection
  • Type C Phospholipases / chemistry*
  • Type C Phospholipases / genetics*

Substances

  • Isoenzymes
  • Chloramphenicol O-Acetyltransferase
  • Single-Strand Specific DNA and RNA Endonucleases
  • Type C Phospholipases
  • PLCB2 protein, human
  • Phospholipase C beta