The use of complementary RNA sequences such as antisense RNAs and ribo
zymes to regulate the expression of specific genes in eukaryotic cells
has been well-documented, particularly with their application to both
human gene therapy and plant biotechnology. Despite the simplicity of
this approach, this technique usually results in only partial suppres
sion of gene expression and, in some instances, even fails to regulate
the gene of interest. The variation observed with antisense RNA and r
ibozyme-mediated regulation is further complicated by the many factors
with the potential to impact on the effectiveness of these RNAs. Rece
nt advances in the understanding of the global architecture of the nuc
leus, chromatin structure, and RNA metabolism provide useful and neces
sary information for designing novel approaches to improving antisense
RNA and ribozyme regulation. These studies predict that the position
of genes within the nucleus is not random and that transcripts produce
d from these genes follow specific tracks in migrating to the cell cyt
oplasm. These observations have the potential to impact significantly
on the ways in which RNA-mediated forms of gene regulation are applied
. The purpose of this review is to discuss the concept of colocalizing
antisense RNAs and ribozymes with their target mRNAs and to introduce
a variety of approaches aimed at achieving this goal.