p73, a recently identified gene, maps to chromosome region 1p36.3, which is
frequently deleted in a variety of solid tumors. Although the gene shares
sequence and functional homologies with p53, its suppressor function has no
t been proven, We investigated for the first time the genetic and expressio
n status of the p73 gene and analyzed its flanking microsatellite loci on c
hromosome 1p36.3 in 67 primary oral and laryngeal squamous cell carcinomas
to determine their association with these tumors. Our results reveal two mi
ssense mutations at codons 469 and 477 and a silent mutation at codon 349 i
n the C-terminal domain, Site-directed mutagenesis of p73 cDNA with these m
utations and a p21 transactivation assay failed to show any significant fun
ctional consequences of these mutations. Microsatellite analysis of the fla
nking loci of p73 in region 1p36 showed overall alterations (loss of hetero
zygosity and instability) frequency of 39%, 16% at the proximal marker and
46% at the distal markers. Of the 21 cases for which we did protein express
ion analyses, 11 tumors had a >2-fold variation compared with matching hist
ologically normal mucosa. Our study shows that: (i) intragenic alterations
in this gene are rare and lack functional significance; (ii) its variable e
xpression argues against a tumor suppressor function; (iii) this gene plays
a minor role in head and neck squamous carcinoma; (iv) a distal site to th
is gene on 1p36 may harbor another suppressor gene.