Cloning and characterization of the TATA-less promoter from the human GFI1 Proto-oncogene

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The growth factor independent 1 (GFI1) gene encodes a zinc finger protein which acts as a transcriptional repressor and confers growth factor independence on tumor cells, as suggested by the study of its mouse ortholog, Gfi1. We previously isolated the human GFI1 gene but no information about the structure and location of the promotor of this gene has been reported. In this study we have cloned and characterized the human GFI1 promoter. The nucleotide sequence of the promoter region is GC-rich and does not contain a typical TATA or CAAT box. Several Sp1 sites are present and computer predictions indicate that either of the two Sp1 sites might serve as the sites for transcription initiation. Analysis of various lengths of the promoter region using the luciferase reporter assay identifies a functional promoter that is active in NIH3T3 cells. The strongest activity lies within a region 312-602 basepairs upstream from the translation start site.

Original languageEnglish (US)
Pages (from-to)83-86
Number of pages4
JournalAnnals of Human Genetics
Volume64
Issue number1
DOIs
StatePublished - Jan 1 2000
Externally publishedYes

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Proto-Oncogenes
Organism Cloning
Intercellular Signaling Peptides and Proteins
Genetic Promoter Regions
Genes
Transcription Initiation Site
Zinc Fingers
Luciferases
Neoplasms
Proteins

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Cloning and characterization of the TATA-less promoter from the human GFI1 Proto-oncogene. / Liu, S.; Cowell, John Kenneth.

In: Annals of Human Genetics, Vol. 64, No. 1, 01.01.2000, p. 83-86.

Research output: Contribution to journalArticle

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