Comparison of mouse and human HOX-4 complexes defines conserved sequences involved in the regulation of Hox-4.4

A. Renucci, V. Zappavigna, J. Zàkàny, J. C. Izpisúa-Belmonte, K. Bürki, D. Duboule*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

59 Scopus citations


We have cloned and sequenced, in both mouse and human, regions of the HOX-4 complex which contain two Abd-B like genes, Hox-4.4 and Hox-4.5 (HOX4C and HOX4D in human, respectively). The high degree of conservation between the homeoprotein sequences extends to non-coding areas, which suggests that the mechanisms of regulation have been conserved. We show that the Hox-4.5/Hox-4.4 intergenic region can be broadly subdivided into three domains based on DNA conservation between rodents and primates. The presence of all these domains in association with sequences located 3′ to the transcription termination site are required to mimick the spatial regulation of Hox-4.4 in transgenic mouse embryos. Several highly conserved short sequences located in this region were studied in gel retardation assays for their binding to potential regulatory factors. One such factor is detected in embryonal carcinoma cells but absent from other differentiated cell lines. This specific binding activity is down regulated upon retinoic acid treatment.

Original languageEnglish (US)
Pages (from-to)1459-1468
Number of pages10
Issue number4
StatePublished - 1992
Externally publishedYes


  • Development
  • HOX-4 complex
  • Homeobox
  • Transgenesis

ASJC Scopus subject areas

  • General Neuroscience
  • Molecular Biology
  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology


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