The replicative retrotransposon life cycle offer's the potential for explos
ive increases in copy number and consequent inflation of genome size. The B
ARE-I retrotransposon family of barley is conserved, disperse, and transcri
ptionally active, To: assess the role of BARE-I in genome evolution, we det
ermined the copy number of its integrase, its reverse transcriptase, and it
s long terminal repeat (LTR) domains throughout the genus Hordeum, On avera
ge, BARE-1 contributes 13.7 x 10(3) full-length copies, amounting to 2.9% o
f the genome. The number increases with genome size. Two LTRs are associate
d with each internal domain in intact retrotransposons, but surprisingly, B
ARE-I LTRs were considerably more prevalent than would be expected from the
numbers of intact elements, The excess in LTRs increases as both genome si
re and BARE-I genomic fraction decrease.: Intrachromosomal homologous recom
bination between LTRs could explain the excess, removing BARE-1 elements an
d leaving behind solo LTRs, thereby reducing the complement of functional r
etrotransposons in the genome and providing at least a partial "return tick
et from genomic obesity,".