Pj. Tatnell et al., MOUSE PROCATHEPSIN-E GENE - MOLECULAR-ORGANIZATION AND CHROMOSOMAL LOCALIZATION, Biochimica et biophysica acta, N. Gene structure and expression, 1398(1), 1998, pp. 57-66
A 15.6 kb genomic clone encompassing the mouse procathepsin E gene was
isolated and mapped. Sequencing revealed that the gene consists of ni
ne exons followed by a polyadenylation signal at the 3'-end. The 5'-fl
anking region appears to be a TATA-less promoter but contains a nucleo
tide sequence that matches perfectly with the consensus motif of an in
itiator element [S.T. Smale, Biochim. Biophys. Acta 1351 (1997) 73-88.
] to direct accurate initiation of transcription by RNA polymerase. Th
is overlaps the site that was determined for the start of transcriptio
n. The absence of features considered typical of TATA-box regulated or
housekeeping types of genes is consistent with the low levels of proc
athepsin E gene expression that are normally observed and might imply
a unique sensitivity to or requirement for tissue-specific transcripti
on factors that would account for the sporadic distribution of this as
partic proteinase in cells and tissues. The single copy of the procath
epsin E gene was located on chromosome 1, near to that of mouse proren
in, a closely related aspartic proteinase involved in blood pressure r
egulation. (C) 1998 Elsevier Science B.V. All rights reserved.