Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1

Citation
Lap. Jurado et al., Identification of a human homolog of the Drosophila rotated abdomen gene (POMT1) encoding a putative protein O-mannosyl-transferase, and assignment to human chromosome 9q34.1, GENOMICS, 58(2), 1999, pp. 171-180
Citations number
28
Categorie Soggetti
Molecular Biology & Genetics
Journal title
GENOMICS
ISSN journal
08887543 → ACNP
Volume
58
Issue
2
Year of publication
1999
Pages
171 - 180
Database
ISI
SICI code
0888-7543(19990601)58:2<171:IOAHHO>2.0.ZU;2-2
Abstract
We have isolated a human gene homologous to Drosophila melanogaster rotated abdomen, rt, a poorly viable recessive mutation causing a clockwise twiste d abdomen in affected flies due to defects in embryonic muscle development, The human gene, like rt, encodes a protein with high homology to the yeast mannosyl-transferases (Pmts) and has been named POMT1. POMT1 is expressed as a 3.1-kb transcript in all tissues tested, with highest levels in testis and fetal brain. Alternative splicing of several exons in all tissues pred icts the generation of several protein isoforms. The most common mRNA varia nt encodes a 725-aa protein with 40% identity and 62.5% similarity to rt, a s well as 30.5% identity and 54% similarity to yeast Pmts. Computer predict ion of protein sorting suggests that the POMT1 product could be an integral protein of the endoplasmic reticulum membrane, Given the strong conservati on of protein motifs between POMT1 and the yeast Pmts, POMT1 may function a s a mannosyl-transferase involved in O-mannosylation of proteins, being the first of such a class found in mammals, The POMT1 locus has been assigned to human chromosome 9q34.1 by somatic cell hybrids, radiation hybrids, and linkage analysis, On the basis of the rt phenotype, POMT1 could be a candid ate for uncharacterized genetic disorders of the muscular system, such as s ome forms of congenital muscular dystrophy or congenital myopathy. (C) 1999 Academic Press.