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Pitx3 promoter directs Cre-recombinase specifically in a human neuroblastoma cell line

  • ,
  • H. Rodríguez-Rocha
    ,
  • R. Montes-de-Oca-Luna
    ,
  • J. Sepúlveda-Saavedra
    ,
  • H.R. Martínez
    ,
  • Y. López-Vidal
  • Universidad Autonoma de Nuevo Leon
    ,
  • Universidad Autónoma de México (UNAM)
Research Output:
Contribution to journal
Article
Peer-review

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Author count
7
SciVal
Paper percentile
37

Abstract

The Pitx3 gene is a homeobox transcription factor. This gene is expressed only in midbrain dopaminergic-neurons in the central nervous system, where its expression is important for development and survival of mesencephalic-dopaminergic neurons. The promoter region of the Pitx3 gene is not yet completely delimited. We used the Cre-loxP system to demonstrate the efficiency and specificity of a 4.2-kbp sequence in the 5′-flanking region of the Pitx3-gene promoter inserted in the 5′-terminus of the Cre-recombinase gene. A Cre-recombinase-reporter assay indicated that this 5′-flanking region possesses promoter activity. The cell-specific gene regulation of the Pitx3 promoter in neurons was demonstrated by a reverse-transcription polymerase chain reaction (RT-PCR) and Western blot detection of Cre-recombinase in SH-SY5Y cells but not in MCF7 cells. Functionality of the Cre-recombinase was confirmed in vitro. The Pitx3-promoter-Cre cassette here described can be used to develop transgenic mice with the specific expression of Cre-recombinase in midbrain-dopaminergic neurons to elucidate the gene function in which the conventional knockout leads to an early lethal phenotype. Such specific expression of the Pitx3 promoter may be used for gene therapy studies of Parkinson's disease.

Publication Information

Output type

Research Output:
Contribution to journal
Article
Peer-review

Original language

English

Pages from-to (Number of pages)

Pages 223-227 (5 pages)

Journal (Volume, Issue Number)

Molecular and Cellular Biochemistry (Volume 309, Issue 1-2)

Publication milestones

  • Published - 02/2008

Publication status

Published - 02/2008

ISSN

0300-8177

Publication IDs

  • ORCID: /0000-0003-2511-949X/work/43281177
  • Scopus: 38649085969
  • WOS: 000252638200025