Aberrant transcripts of FHIT and TSG101 using nested RT-PCR were reported i
n many human tumours. The role of these aberrant transcripts in tumourigene
sis is not clear. We, therefore, analyzed the aberrant transcripts of FHIT,
TSG101 and PTEN/MMAC1 in peripheral mononuclear cells of normal individual
s using nested RT-PCR to explore the role of these genes in cancer developm
ent. The results showed that there are at least five types of aberrant tran
scripts: type I is the deletion at junction located in-between normal exon
and intron; type II has deletion of some bases and subsequent insertion of
several bases in the deletion area; type III accommodates splicing donor or
acceptor site-like sequence; type IV has homologous sequences near the del
eted junction; and type V comprises the homologous sequences at the deletio
n junction. A normal healthy person can have more than one aberrant transcr
ipts of FHIT, TSG101 and PTEN/MMAC1 genes. The size and the number of the t
ranscripts vary and the diversity is unconstrained. It is not depended on t
he time, condition of the reaction, or the isolation method. From these res
ults, we suggested that the aberrant transcripts of FHIT, TSG101 and PTEN/M
MAC1 genes may be the imperfect products of splicesome which occur one in e
very thousands, ten thousands or more. As a result, these data implied no d
irect association between the aberrant transcripts and tumourigenesis.