CHARACTERIZATION OF THE HUMAN P57(KIP2) GENE - ALTERNATIVE SPLICING, INSERTION DELETION POLYMORPHISMS IN VNTR SEQUENCES IN THE CODING REGION, AND MUTATIONAL ANALYSIS
T. Tokino et al., CHARACTERIZATION OF THE HUMAN P57(KIP2) GENE - ALTERNATIVE SPLICING, INSERTION DELETION POLYMORPHISMS IN VNTR SEQUENCES IN THE CODING REGION, AND MUTATIONAL ANALYSIS, Human genetics, 97(5), 1996, pp. 625-631
We have isolated human cDNA and genomic clones of a gene termed p57(KI
P2), which is related to the p21(WAF1) and p27(KIP1) genes that encode
inducible inhibitors of cyclin-dependent kinase activity. The p57 gen
e contains three GC-rich introns of 166 bp, 566 bp, and 83 bp, and two
of the four exons correspond to coding regions. Alternative splicing
generates the heterogeneity in the translational initiations. As this
gene has been localized to chromosomal band 11p15.5, a region thought
to be the location of a tumor suppressor gene(s) for carcinomas of the
breast, bladder, and liver, we have examined a large number of tumors
for genetic alterations of p57. Although no somatic mutation has been
detected, we have found several normal variations in this gene, inclu
ding four types of 12-bp in-frame deletions in the proline/alanine rep
eating domain, in which nearly 40 motifs, viz., 5'CCGGCC-3', are tande
mly repeated.