ALTERNATIVE SPLICING OF AMELOGENIN MESSENGER-RNA FROM RAT INCISOR AMELOBLASTS
Citation
R. Li et al., ALTERNATIVE SPLICING OF AMELOGENIN MESSENGER-RNA FROM RAT INCISOR AMELOBLASTS, Journal of dental research, 74(12), 1995, pp. 1880-1885
Categorie Soggetti
Dentistry,Oral Surgery & Medicine
SICI code
0022-0345(1995)74:12<1880:ASOAMF>2.0.ZU;2-Y
Abstract
Amelogenin proteins are a major component of the developing enamel mat
rix, and are likely to have a key role in the control of enamel biomin
eralization. The heterogeneity of amelogenin is in part due to alterna
tive splicing of the amelogenin RNA transcripts. Several patterns of a
lternative splicing have been described in mouse, bovine, porcine, and
human enamel, with all alternatively spliced products having homologo
us 5' and 3' sequences within the coding regions. In these studies, we
have used anchored PCR to identify alternatively spliced amelogenin c
DNA sequences in the rat. We found amelogenin cDNAs that could be divi
ded into two groups based on their 3' sequence. Group 1 cDNAs had a no
vel terminal sequence that has not been previously identified, while g
roup 2 cDNAs were similar to those previously identified in other anim
al species. We identified a sequence, identical to the novel 3' amelog
enin cDNA sequence, in rat genomic DNA downstream from the previously
identified exon 7. The putative amelogenin proteins predicted for the
two groups differed in their predicted isoelectric points, with the no
vel group 1 proteins having a more basic isoelectric point.