Transcriptional regulation of the MHC class I genes leading to their develo
pmental and tissue specific expression is still poorly understood in spite
of the recovery of a large variety of cis-controlling sequences and trans-a
cting factors pertaining to the 5' enhancer and the downstream regulatory e
lement. Here we produced a series transgenic lines of mice with a genomic s
ubclone of the H2-K-b gene consisting of 367 bp of the 5' upstream region,
the coding region and 1.5 kb of the 3' downstream region and carrying all h
itherto known regulatory sequences. The comparison of nine transgenic lines
carrying the same H2-K-b transgene made it possible to ask whether the cis
-information present in the transgene was sufficient for the tissue- and de
velopmental-specific expression and its copy number dependence. We found th
e proper developmental onset of expression of the transgene at day 13 p.c.
and correct tissue specific mRNA levels in adult mice. While in lymphoid ti
ssues and in lung the number of transgene copies still correlated with RNA
levels, the copy number dependence was completely lost in liver, kidney and
embryonic tissues. Comparison with previously published H2-K-b transgenes
indicates that the H2-K-b locus-controlling region is composed of more than
one element. (C) 1999 Elsevier Science Ltd. All rights reserved.