PML, a Ring-finger protein, participates in the disruption of normal m
yeloid differentiation when fused to the retinoic acid receptor alpha
(RAR alpha) by the translocation between Chromosomes (Chrs) 15 and 17
in acute promyelocytic leukemia (APL). As an initial step in the chara
cterization of PML in species other than human, a murine cDNA clone of
the PML gene was isolated and sequenced, and the intron/exon organiza
tion of the murine locus determined. The predicted amino acid sequence
of the mouse PML protein shows 80% similarity to that of its human ho
molog. However, the mouse and human proteins show greater than 90% sim
ilarity in the proposed functional domains of the proteins. Despite it
s role in the etiology of APL, PML expression is not detectably altere
d during granulocytic differentiation in a murine in vitro system. Chr
omosomal localization of the Pml locus by somatic cell hybrids and by
linkage analysis indicates that the gene maps to a region of mouse Chr
9 with known linkage homology to the region on human Chr 15q to which
PML has been localized.