Mc. Walters et al., The chicken beta-globin 5 ' HS4 boundary element blocks enhancer-mediated suppression of silencing, MOL CELL B, 19(5), 1999, pp. 3714-3726
A constitutive DNase I-hypersensitive site 5' of the chicken beta-globin lo
cus, termed 5'HS4 or cHS4, has been shown to insulate a promoter from the e
ffect of an upstream enhancer and to reduce position effects on mini-white
expression in Drosophila cells; on the basis of these findings, it has been
designated a chromatin insulator. We have examined the effect of the cHS4
insulator in a system that assays both the level of gene expression and the
rate of transcriptional silencing. Because transgenes flanked by insulator
elements are shielded from position effects in Drosophila cells, we tested
the ability of cHS4 to protect transgenes from position effects in mammali
an cells. Flanking of an expression vector with the cHS4 insulator in a col
ony assay did not increase the number of G418-resistant colonies. Using lox
/cre-based recombinase-mediated cassette exchange to control integration po
sition, we studied the effect of cHS4 on the silencing of an integrated bet
a-geo reporter at three genomic sites in K562 erythroleukemia cells. In thi
s assay, enhancers act to suppress silencing but do not increase expression
levels. While cHS4 blocked enhancement at each integration site, the stren
gth of the effect varied from site to site. Furthermore, at some sites, cHS
4 inhibited the enhancer effect either when placed between the enhancer and
the promoter or when placed upstream of the enhancer. These results sugges
t that the activity of cHS4 is not dominant in all contexts and is unlikely
to prevent silencing at all genomic integration sites.