Jmw. Geurts et al., IDENTIFICATION OF NFIB AS RECURRENT TRANSLOCATION PARTNER GENE OF HMGIC IN PLEOMORPHIC ADENOMAS, Oncogene, 16(7), 1998, pp. 865-872
Approximately 12% of all pleomorphic adenomas of the salivary glands a
re characterized by chromosome aberrations involving the chromosome se
gment 12q13-15. Several chromosomes have been found as translocation p
artners of chromosome 12, and some of these recurrently. Recently, the
HMGIC gene was identified as the target gene affected by the 12q13-15
aberrations. Here, me report the identification and characterization
of a new translocation partner gene of HMGIC in pleomorphic adenomas,
3'-RACE analysis of a primary adenoma with an apparently normal karyot
ype revealed an HMGIC fusion transcript containing ectopic sequences d
erived from the human NFIB gene, previously mapped to chromosome band
9p24.1. The HMGIC NFIB fusion transcript was also confirmed by RT-PCR,
Since the chromosome segment 9p12-24 is repeatedly involved as transl
ocation partner of chromosome 12q13-15 in pleomorphic adenomas, we tes
ted whether NFIB might be a recurrent partner of HMGIC, RT-PCR analysi
s of a second adenoma with an ins(9;12)(p23;q12q15) as the sole anomal
y, revealed that also in this tumor an HMGIC/NFIB hybrid transcript wa
s present, The reciprocal NFIB/HMGIC fusion transcript, however, could
not be detected in any of these tumors, Nucleotide sequence analysis
of the fusion transcripts indicated that the genetic aberration in bot
h tumors resulted in the replacement of a carboxy-terminal segment of
HMGIC by the last five amino acids of NFIB. In conclusion, our results
reveal the recurrent involvement of the NFIB gene as translocation pa
rtner gene of HMGIC in pleomorphic adenomas.