Recapitulation of human betaB1-crystallin promoter activity in transgenic zebrafish. Journal Article uri icon



  • Development of the eye is morphologically similar among vertebrates, indicating that the underlying mechanism regulating the process may have been highly conserved during evolution. Herein we analyzed the promoter of the human betaB1-crytallin gene in zebrafish by transgenic experiments. To delineate the evolutionarily conserved regulatory elements, we performed serial deletion assays in the promoter region. The results demonstrated that the -90/+61-bp upstream proximal promoter region is sufficient to confer lens-tissue specificity to the human betaB1-crystallin gene in transgenic zebrafish. Through phylogenetic sequence comparisons and an electrophoretic mobility shift assay (EMSA), a highly conserved cis-element of a six-base pair sequence TG(A/C)TGA, the consensus sequence for the Maf protein binding site, within the proximal promoter region was revealed. Further, a site-mutational assay showed that this element is crucial for promoter activity. These data suggest that the fundamental transcriptional regulatory mechanism of the betaB1-crystallin gene has been well conserved between humans and zebrafish, and plausibly among all vertebrates, during evolution.

publication date

  • February 1, 2006

has subject area

has restriction

  • closed

Date in CU Experts

  • November 15, 2013 1:55 AM

Full Author List

  • Hou H-H; Kuo MY-P; Luo Y-W; Chang B-E

author count

  • 4

Other Profiles

International Standard Serial Number (ISSN)

  • 1058-8388

Additional Document Info

start page

  • 435

end page

  • 443


  • 235


  • 2