Cy. Liu et al., CHARACTERIZATION AND CHROMOSOMAL LOCALIZATION OF THE CORNEA-SPECIFIC MURINE KERATIN GENE KRT1.12, The Journal of biological chemistry, 269(40), 1994, pp. 24627-24636
Keratins are a group of water-insoluble proteins constituting paired a
cidic and basic keratin molecules that form 10-nm intermediate filamen
ts in epithelial cells. Expression of the K3/K12 keratin pair characte
rizes the cornea-type differentiation. However, the mechanism that reg
ulates this cornea-specific K12 expression remains unknown. To provide
a better understanding of the cornea-specific expression, we have clo
ned the K12 cDNA (Liu, C.-Y., Zhu, G., Westerhausen-Larson, A., Conver
se, R., Kao, C. W.-C., Sun, T.-T., and Kao, W. W.-Y. (1993) Curr. Eye
Res. 12, 963-974). In present studies, the murine K12 keratin gene (Kr
t1.12) was isolated and characterized. The murine Krt1.12 gene spans 6
,567 base pairs of genomic DNA, and the mRNA encoding K12 keratin is d
istributed into eight exons. Chromosome mapping reveals that murine Kr
t1.12 is located within the Krt1 complex of mouse chromosome 11. In ad
dition to the production of authentic K12 mRNA, the Krt1.12 gene gives
rise to several alternate poly(A)(+) RNAs by the use of alternative s
plicing in intron 2, an alternative pro meter in intron 1, and/or both
. Sequence analysis indicates that the transcripts derived from altern
ative splicing and/or the alternative promoter do not have a long open
reading frame for keratin or keratin-like molecules. It is not known
whether these alternate K12 poly(A)(+) RNAs have any biological functi
ons, e.g. regulation of K12 gene expression.