Radiation hybrid (RH) mapping of the mouse genome provides a useful tool in
the integration of existing genetic and physical maps, as well as in the o
ngoing effort to generate a dense map of expressed sequence tags. To facili
tate functional analysis of mouse Chromosome 5, we have constructed a high-
resolution RH map spanning 75 cM of the chromosome. During the course of th
ese studies, we have developed RHBase, an RH data management program that p
rovides data storage and an interface to several RH mapping programs and da
tabases. We have typed 95 markers on the T31 RH panel and generated an inte
grated map, pooling data from several sources. The integrated RH map ranges
from the most proximal marker, D51Mit331 (Chromosome Committee offset, 3 c
M), to D5Mit326, 74.5 cM distal on our genetic map (Chromosome Committee of
fset, 80 cM), and consists of 138 markers, including 89 simple sequence len
gth polymorphic markers, 11 sequence-tagged sites generated from BAC end se
quence, and 38 gene loci, and represents average coverage of approximately
one locus per 0.5 cM with some regions more densely mapped. In addition to
the RH mapping of markers and genes previously localized on mouse Chromosom
e 5, this RH map places the alpha-4 GABA(A) receptor subunit gene (Gabra4)
in the central portion of the chromosome, in the vicinity of the cluster of
three other GABA(A) receptor subunit genes (Gabrg1-Gabra2-Gabrb1). Our map
ping effort has also defined a new cluster of four genes in the semaphorin
gene family (Sema3a, Sema3c, Sema3d, and Sema3e) and the Wolfram syndrome g
ene (Wfs1) in this region of the chromosome. (C) 2000 Academic Press.