Current knowledge of genes that regulate pattern formation and differe
ntiation processes during mammalian embryonic development is limited.
In an effort to isolate developmentally relevant genes, 20 novel, end-
sequenced cDNAs selected from a Day 10.5 post-coitum mouse embryo libr
ary were genetically mapped in intersubspecific backcross mice. Eleven
of 20 cDNA clones mapped to three mouse autosomes (Chr 5, 11, and 14)
, a result that was unlikely (P < 0.03) if the distribution of genes e
xpressed in embryos is random within the mouse genome. Several clones
were candidates for mouse developmental mutations by virtue of genetic
colocalization and concordance of embryonic expression patterns with
the distribution of defects in mutant mice: Estm11 was a candidate for
the mouse mutation wabbler-lethal (wl), since Estm11 mapped in the vi
cinity of wl on mouse Chr 14 and was expressed in those regions of emb
ryonic brain that exhibit axonal degeneration in wt. End-sequence anal
ysis, genetic mapping, and in situ hybridization appeared to be an eff
ective combination of methods for identification and characterization
of genes with potential regulatory functions during mammalian embryoge
nesis. (C) 1997 Academic Press.