Wheat telomere-associated sequences (TASs) were cloned using a Vectore
tte approach and sequenced. Reverse primers specific to the TASs were
combined with labelled degenerate telomere primers in PCR reactions co
ntaining total genomic DNA as template. Amplification products were se
parated on sequencing gels. In total, seventeen primer combinations pr
ovided 47 polymorphic fragments. Nine of these mapped beyond the most
distal RFLP markers and defined the ends of seven chromosome arms. Sev
en of the nine terminal fragments were derived from a 118-bp tandem re
peat, indicating that subtelomeric tandem repeat sequences provide an
efficient means to target chromosome ends. A telomere cloning strategy
and the terminal and interstitial location of TASs are discussed.