The biological meaning of abundant simple repetitive DNA sequences in
eukaryote genomes is obscure. Therefore, (GAA)(n), (GT)(n), and compos
ite (GT)(n)(GA)(m) blocks were characterized for protein binding in th
e repeat and flanking sequences of cloned genomic DNA fragments. In ge
l mobility shift and competition assays the binding of nuclear protein
s to the repeats was specific (including some flanking single copy seq
uences). DNase footprinting revealed the target sequences within and a
djacent to the repeats. Chemical modifications (OsO4, DEPC) demonstrat
ed non-B DNA structures in the polypurine blocks. The binding of nucle
ar proteins in and around simple repeat sequences refute biological in
significance of all of these ubiquitously interspersed elements.