To investigate the cellular action of the Mi(wh) allele in the mouse w
ith regard to its effects upon coat color patterns, we generated a ser
ies of aggregation chimeras, using embryos that differ in their mi loc
us genotype. We have obtained 11 chimeras Mi(wh)/+ C/C <-> +/+ c/c and
8 chimeras +/+ C/C <-> +/+ c/c. Chimerism was determined by coat and
retinal pigment epithelium mosaicism and by the electrophoretic analys
is of GPI-1 isoenzymes. In Mi(wh)/+ C/C <-> +/+ c/c mice white coat co
lor prevailed due to the higher percentage of unpigmented areas and th
e higher percentage of unpigmented hairs in pigmented areas. Our data
indicate that a single Mi(wh) gene dose decreases the melanoblast prol
iferative activity, causing the lightening of coat pigmentation. In Mi
(wh)/+ C/C <-> +/+ c/c mice a few pigmented hairs were often detected
on the belly where Mi(wh) / + mice always had a white spot. This sugge
sts that in the chimeras the presence of some non-Mi(wh) cells in the
skin of the belly allows pigment cells to develop. Using embryos of tw
o substrains of Mi(wh)/Mi(wh) mice that differ in their Gpi-1 locus ge
notype we have produced 8 Mi(wh)/+ <-> Mi(wh)/Mi(wh) chimeras. In all
these chimeras coat color patterns resembled those of Mi(wh)/+ heteroz
ygotes despite the higher percentage of the Mi(wh)/Mi(wh) component in
three chimeras. Mosaic hairs were absent in the chimeras. This shows
that the chimeras have only one Mi(wh)/+ melanoblast population which
actively proliferates and colonizes almost all hair follicles. Thus th
e Mi)(wh)/Mi(wh) dermis and epidermis do not suppress proliferation an
d differentiation of the Mi(wh)/+ melanoblasts except the certain area
on the belly.