Nucleic Acids Research, Vol 24, Issue 12 2295-2301, Copyright © 1996 by Oxford University Press
H Alexander, SK Lee, SL Yu and S Alexander
We have cloned and characterized the Dictyostelium discoideum repE gene, a
homolog of the human xeroderma pigmentosum (XP) group E gene which encodes
a UV-damaged DNA binding protein. The repE gene maps to chromosome 4 and it
is the first gene identified in Dictyostelium that is homologous to those
involved in nucleotide excision repair and their related XP diseases in
humans. The predicted protein encodes a leucine zipper motif. The repE gene
is not expressed by mitotically dividing cells, and repE mRNA is first
detected during the aggregation phase of development when the cells have
ceased dividing and replicating genomic DNA. The mRNA level plateaus by the
time the developing cells have entered multicellular aggregates and remains
at the same steady-state level for the remainder of development. In
addition, we have demonstrated that the level of mRNA is very low in
developing cells. These observations suggest that repE may play a
regulatory role in development. The data indicate that potential
developmental roles for XP-related genes can be profitably studied in this
system.
ARTICLES
repE--the Dictyostelium homolog of the human xeroderma pigmentosum group E gene is developmentally regulated and contains a leucine zipper motif
Division of Biological Sciences, University of Missouri, Columbia, MO 65211, USA.
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