Abstract
Mast cells derived from haematopoietic tissue are deficient in numbers in spleen, stomach and skin of Harwell mice doubly mutant at the spotting
W
locus: seven viable combinations of four mutants. Most combinations have variably impaired viability, anaemia and infertility; but homozygous
W
sh
W
sh
are normal in these respects yet still lack mast cells. The effect of the
W
gene on mast cells acts in recessive fashion. Effects of doubly mutant
W
genes on mast cells and coat colour, the latter usually regarded as dominant, appear more closely related than other pleiotropic effects. The spotting gene
Ph
, closely linked to
W
, has but marginal effects on mast cells, whereas
mi
, another spotting gene, quite unrelated to
W
affects mast cells in the spleen in a dominant way. Thus, splenic mast cells may be a special category of a heterogeneous population. Peptic ulceration, recorded in
W/W
v
mice of Jackson stock, was not seen in Harwell mice. We suggest that this lesion is due to genetic complementation or environmental causes.
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