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Tissue-specific Expression Patterns and Fine Mapping of the Human Kallikrein (KLK) Locus on Proximal 19q13.4
Citation
Harvey, TJ and Hoopert, JD and Myers, SA and Stephenson, S-A and Ashworth, L and Clements, JA, Tissue-specific Expression Patterns and Fine Mapping of the Human Kallikrein (KLK) Locus on Proximal 19q13.4, International Journal of Biological Chemistry, 275, (48) pp. 37397-37406. ISSN 1819-155X (2000) [Refereed Article]
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Copyright Statement
Copyright 2000 American Society for Biochemistry and Molecular Biology
DOI: doi:10.1074/jbc.M004525200
Abstract
The tissue or glandular kallikreins (KLK) are members
of a highly conserved multigene family encoding
serine proteases that are central to many biological processes.
The rodent KLK families are large, highly conserved
and clustered at one locus. The human KLK gene
family is clustered on chromosome 19q13.3–13.4, and until
recently consisted of just three members. However,
recent studies have identified up to 11 new members of
the KLK family that are less conserved than their rodent
counterparts. Using a Southern blot and sequence analysis
of 10 BACs and cosmids spanning approximately
400 kilobases (kb) either side of the original KLK 60-kb
locus, we demonstrated that these genes also lie adjacent
to this. We have also clarified the position of several
microsatellite markers in relation to the extended KLK
locus. Moreover, from Southern blot analysis of the cosmids
and BACs with a degenerate oligonucleotide probe
to the histidine-encoding region of serine proteases, we
have shown that there are no other serine protease
genes approximately 400 kb centromeric and 220 kb telomeric
of the extended locus. We performed an extensive
analysis of the expression patterns of these genes by
poly(A)1 RNA dot blot and reverse transcriptase-polymerase
chain reaction analysis, and demonstrated a diverse
pattern of expression. Of interest are clusters of
genes with high prostate (KLK2–4) and pancreatic
(KLK6–13) expression suggesting evolutionary conservation
of elements conferring tissue specificity. From
these findings, it is likely that the human KLK gene
family consists of just 14 clustered genes within 300 kb
and thus is of a comparable size to the rodent families
(13–24 genes within 310 and 480 kb, respectively). In
contrast to the rodent families, the newest members of
the human KLK family are much less conserved in sequence
(23–44% at the protein level) and appear to consist
of at least four subfamilies. In addition, like the rat,
these genes are expressed at varying levels in a diverse
range of tissues although they exhibit quite distinct patterns
of expression
Item Details
Item Type: | Refereed Article |
---|---|
Keywords: | Kallikrein, Locus mapping |
Research Division: | Biological Sciences |
Research Group: | Genetics |
Research Field: | Genomics |
Objective Division: | Health |
Objective Group: | Clinical health |
Objective Field: | Clinical health not elsewhere classified |
UTAS Author: | Myers, SA (Dr Stephen Myers) |
ID Code: | 100901 |
Year Published: | 2000 |
Web of Science® Times Cited: | 137 |
Deposited By: | Health Sciences B |
Deposited On: | 2015-06-03 |
Last Modified: | 2015-06-12 |
Downloads: | 399 View Download Statistics |
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