The expansion of heterochromatin blocks in rye reflects the co-amplification of tandem repeats and adjacent transposable elements

Table 1 Percent identity of pSc200 monomers present in BAC clone 119C15

Sequence of the pSc200 monomers in contig	fr47-1	fr47-2	exo2-1	T79-1	T79-2	exo6-1	exo7-1	T713-1	exo9-1	exo9-2	T7-6
fr47-1	100	89.36	95.77	88.56	95.23	89.04	98.41	88.86	95.49	89.36	95.77
fr47-2		100	90.16	96.55	89.33	97.60	90.43	99.47	89.36	96.82	89.92
exo2-1			100	90.16	98.41	89.84	96.83	89.66	98.41	90.69	98.94
T79-1				100	89.33	96.27	89.63	96.02	89.10	97.61	89.92
T79-2					100	89.01	96.82	88.83	98.94	89.87	99.47
exo6-1						100	90.11	97.07	89.07	97.07	89.60
exo7-1							100	89.92	97.08	90.43	97.35
T713-1								100	88.86	96.29	89.39
exo9-1									100	89.63	99.73
exo9-2										100	90.45
Т7-6											100

Fragment of the pSc200 array from DNA BAC199C15 was sub-cloned in a plasmid vector pGem-5Zf(+). Then a series of deletion clones was obtained according to [24] and their inserts were sequenced and assembled into a contig encompassing 11 full-length monomers of pSc200

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