B-lymphoid and myeloid development are markedly perturbed in a unique
transgenic mouse strain, max 41. Pro-B, pre-B, and B lymphocytes were
severely reduced but granulocytes were greatly elevated. This phenotyp
e could be adoptively transferred with bone marrow cells. It was not a
lleviated by bcl-2 or myc transgenes that promote lymphocyte survival
or proliferation. Bitransgenic myc/max 41 mice developed pre-B cell ly
mphoma. An accompanying massive granulocytosis unexpectedly proved to
be clonally derived from the pre-B lymphoma cells. These observations
suggest that B lymphopoiesis in max 41 mice has been diverted to granu
locyte production. Since neither cell type expressed the transgene, th
is novel lymphomyeloid deviation probably reflects insertional alterat
ion of a hematopoietic regulatory gene.