Fig. 2. The Lfng
FCE1 allele
interferes with normal skeletal development during primary body formation.
(A) Representative phenotypes of Lfng+/-,
Lfng
FCE1/
FCE1 and
Lfng-/- mice. The
Lfng
FCE1/
FCE1 mouse has a shortened body and
kinked tail. (B) Skeletal preparations of wild-type (a,b,g),
Lfng
FCE1/
FCE1 (c,d,h) and
Lfng-/- (e,f,i) mice. Ventral (a,c,e) and dorsal (b,d,f)
views of the ribs and dorsal views of the lumbar and sacral spine (g-i) are
shown. The thoracic regions of Lfng
FCE1/
FCE1
(c,d) and Lfng-/- (e,f) mice exhibit rib fusions (arrows)
and disorganized vertebrae. In Lfng
FCE1/
FCE1
skeletons, vertebral disorganization extends through the lumbar region (bar,
h), but normal vertebral condensations are seen in the sacral spine
(*). By contrast, vertebral disorganization extends throughout the
lumbar (bar) and sacral (*) regions of Lfng-/-
skeletons (i), and the tail appears severely truncated. (C) Rib
abnormalities were quantified in Lfng wild-type (n=17),
Lfng
FCE1/
FCE1 (n=11) and
Lfng-/- (n=8) neonates. Results are shown as bar
and whisker graphs (solid horizontal line indicates the mean), with the number
of rib abnormalities indicated on the y-axis. The number of rib
abnormalities is similar in Lfng-/- and
Lfng
FCE1/
FCE1 animals (P=0.236, the
null hypothesis is accepted). (D) Tail anomalies were quantified in
adult animals. The proportion of animals with 0-1 kinks, 2-5 kinks or
truncated tails are shown. Forty percent of
Lfng
FCE1/
FCE1 animals exhibit mild tail
defects (0-1 kinks), while the remaining animals had between 2 and 5 kinks. By
contrast, Lfng-/- animals exhibit truncation in the tail
region.