Kk. Wilgenbus et al., STRUCTURE AND LOCALIZATION ON THE X-CHROMOSOME OF THE GENE CODING FORTHE HUMAN FILOPODIAL PROTEIN MOESIN (MSN), Genomics, 19(2), 1994, pp. 326-333
Moesin is a member of a recently discovered family of closely related
proteins that includes ezrin, radixin, and merlin. It is widely expres
sed in different tissues and cells and has been localized to filopodia
and other membranous protrusions that are important for cell-cell rec
ognition and signaling and cell movement. Here, we have localized the
coding gene (MSN) to Xq11.2-q12 by Southern and Western blot analyses
of Chinese hamster X human somatic cell hybrids and by fluorescence ch
romosomal in situ hybridization. Moesin-like sequences were identified
on chromosomes 5 and 6. The murine Msn locus was mapped to the X chro
mosome as well by studying a rodent X mouse hybrid panel. The structur
e of the human moesin gene has been determined. The 12 exons are distr
ibuted over,30 kb, and the exon/intron junctions demarcate individual
highly conserved domains. Primer extension analysis revealed two major
start transcription sites, 184 and 133 bp upstream of the initiation
codon. The 5'-flanking region is CC-rich, lacks a TATA box, and contai
ns four SP1 and one AP1 binding sites. (C) 1994 Academic Press, Inc.