The mammalian chromosome is longitudinally heterogeneous in structure
and function and this is the basis for the specific banding patterns p
roduced by various chromosome staining techniques. The two most freque
ntly used techniques are G, or Giemsa banding and R, or reverse bandin
g. Each type of stained band is characterised by variations in gene de
nsity, time of replication, base composition, density of repeat sequen
ces, and chromatin packaging. It is increasingly apparent that R and G
bands, which are complementary to each other, represent separate comp
artments of the euchromatic human genome, with R bands containing the
vast majority of genes. R bands are also more GC-rich, contain a highe
r density of Alu repeats, and replicate earlier in S phase, than G ban
ds. These properties may be interdependent and may have coevolved.