L. Ramsay et al., Intimate association of microsatellite repeats with retrotransposons and other dispersed repetitive elements in barley, PLANT J, 17(4), 1999, pp. 415-425
Simple sequence repeat (SSR)-based genetic markers are being actively devel
oped for the majority of crop plant species. In barley, characterization of
290 dinucleotide repeat-containing clones from SSR-enriched libraries has
revealed that a high percentage are associated with cereal retrotransposon-
like and other dispersed repetitive elements. Associations found were with
BARE-1, WIS2-1A, PREM1 and the dispersed repetitive element R173. Additiona
l similarities between different SSR clones, which have no matches in DNA s
equence databases, indicate that this phenomenon is probably widespread in
the barley genome. Sequence homologies to the non-coding regions of several
cereal genes were also explained by homology to mobile genetic elements. T
he SSRs found can therefore be classified into two types: (1) those with un
ique sequences on either flank, and (2) those which are intimately associat
ed with retro-transposons and other dispersed repetitive elements. As the c
ereal genome is thought to consist largely of this type of DNA, some random
association would be expected. However, the conserved positions of the SSR
s, relative to repetitive elements, indicate that they have arisen non-rand
omly. Furthermore, this class of SSRs can be classified into three subtypes
: (1) those which are positioned 3' of a transposable element with unique s
equence on the other flank, (2) those positioned 5' of a transposable eleme
nt, and (3) those which have arisen from an internal sequence and so have t
ransposable element sequence on both flanks. The first appear to be analogo
us to the class of SSRs in mammalian systems which are associated with Alu
elements and SINEs (short interspersed elements) and which have been postul
ated to arise following integration of an extended and polyadenylated retro
-transcript into the host genome, followed by mutation of the poly(A) tract
and expansion into an SSR. For the second, we postulate that a proto-SSR (
A-rich sequence) has acted as a 'landing pad' for transposable element inse
rtion (rather than being the result of insertion), while the third includes
those which have evolved as a component of an active transposable element
which has spread throughout the genome during bursts of transposition activ
ity. The implications of these associations for genome and SSR evolution in
barley are discussed.