Identification and sequencing the juvenile spermatogonial depletion critical interval on mouse chromosome 1 reveals the presence of eight candidate genes
Hl. Boettger-tong et al., Identification and sequencing the juvenile spermatogonial depletion critical interval on mouse chromosome 1 reveals the presence of eight candidate genes, BIOC BIOP R, 288(5), 2001, pp. 1129-1135
Citations number
17
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
In mice, the recessive, non-pleiotropic, juvenile spermatogonial depletion
(jsd) mutation results in a single wave of spermatogenesis, followed by fai
lure of type A spermatogonial stem cells to differentiate, rendering adult
males sterile. As part of an effort to identify the gene underlying this mu
tation, we report here the construction of a high-resolution genetic map in
volving more than 1000 meioses and 24 polymorphic loci. Our data define a c
ritical jsd interval of approximately 0.4 cM at 49 cM on mouse chromosome 1
, between D1Mit215 and 257SP6. We have constructed a physical map spanning
the region comprising 24 overlapping BACs. Eighteen of these BACs have been
fully sequenced, or are in draft form, allowing us to annotate approximate
ly 2.5 Mb of DNA surrounding the jsd locus. The critical 0.4 cM jsd interva
l corresponds to a physical distance of similar to1.5 Mb. Eight genes have
been identified in this interval, two of which appear to be possible candid
ates for the jsd mutation. (C) 2001 Academic Press. Press.