p33/ING1s (the growth inhibitor ING1 and candidate tumor suppressor ING1) a
re key players in the suppressive pathways for human tumorigenesis. We anal
yzed their complete transcripts, primary structures, and expression. The re
sults led us to discover two novel and related alternatively spliced transc
ripts encoding p24/ING1-ALT1 and p47/ING1-ALT2. They share C-terminal resid
ues with the candidate tumor suppressors p33/ING1. The candidate tumor supp
ressors p33/ING1 and p24/ING1-ALT1 were coexpressed in a variety of fetal a
nd adult human tissues, but p47/ING1-ALT2 was minimally expressed.