Cf. Fletcher et al., MOUSE CHROMOSOMAL LOCATIONS OF 9 GENES ENCODING HOMOLOGS OF HUMAN PARANEOPLASTIC NEUROLOGIC DISORDER ANTIGENS, Genomics, 45(2), 1997, pp. 313-319
The paraneoplastic neurologic disorders (PND) are a rare group of neur
ologic syndromes that arise when an immune response to systemic tumors
expressing neuronal proteins (''onconeural antigens'') develops into
an autoimmune neuronal degeneration. The use of patient antisera to cl
one the genes encoding PND antigens has led to new insight into the me
chanism of these autoimmune disorders. The tumor antigens can now be g
rouped into three classes: (1) neuron-specific RNA-binding proteins, (
2) nerve terminal vesicle-associated proteins, and (3) cytoplasmic sig
naling proteins. To understand better the evolutionary relatedness of
these genes and to evaluate them as candidates for inherited neurologi
cal disorders, we have determined the mouse chromosomal locations of n
ine of these genes-Hua, Hub, Hue, Hud, Nova1, Nova2, Natpb, Cdr2, and
Cdr3. These data suggest that the Hua-Hud genes arose from gene duplic
ation and dispersion, while the other genes are dispersed in the genom
e. We also predict the chromosomal locations of these genes in human a
nd discuss the potential of these genes as candidates for uncloned mou
se and human mutations. (C) 1997 Academic Press.