Human Molecular Genetics, 2002, Vol. 11, No. 7 799-804
© 2002 Oxford University Press
Gain-of-function mutation in ADULT syndrome reveals the presence of a second transactivation domain in p63
Department of Human Genetics 417, University Medical Centre Nijmegen, Box 9101, 6500 HB Nijmegen, The Netherlands, 1Human Genetics Institute, Rheinische Friedrich-Wilhelms University, Wilhelmstrasse 31, 53111 Bonn, Germany, 2CMBI, University of Nijmegen, Box 9010, 6500 GL Nijmegen, The Netherlands, 3Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA and 4Department of Pharmaceutical Chemistry, University of California, San Francisco, CA, USA
The transcriptional co-activator p63 is of crucial importance for correct development of the limbs, ectodermal appendages (skin, nails, teeth, hair, glands), lip and palate. Mutations in the p63 gene are found in a number of human syndromes, including ectrodactyly-ectodermal dysplasia-cleft lip/palate (EEC) syndrome, limb-mammary syndrome (LMS), HayWells syndrome and in non-syndromic split-hand/split-foot malformation (SHFM). Each syndrome has a specific pattern of mutations with different functional effects in in vitro functional assays. We report a mutation R298Q in acro-dermato-ungual-lacrimal-tooth (ADULT) syndrome, another EEC-like condition. The mutation is located in the DNA binding domain of p63, which harbors almost all EEC associated mutations. However, unlike mutations in EEC syndrome, the R298Q ADULT syndrome mutation does not impair DNA binding. Rather, the mutation confers novel transcription activation capacity on the
N-p63
isoform, which normally does not possess such activity. These results confirm that ADULT syndrome is a clinically as well as molecularly distinct member of the expanding p63 mutation family of human malformation syndromes. Our results further show that p63 contains a second transactivation domain which is normally repressed and can become activated by mutations in the DNA binding domain of p63.
+ To whom correspondence should be addressed. Tel: +31 24 3614017; Fax: +31 24 3540488; Email: h.vanbokhoven@antrg.azn.nl
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