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. 2014 May 9;6(6):1335–1352. doi: 10.1093/gbe/evu096

Fig. 3.—

Fig. 3.—

Sequence relationship of recombinant sorghum CR5 and Setaria CR1 elements to their respective parents. The CR elements are drawn to scale, and vertical bars mark the ends of the 5′-LTR, 5′-UTR, polypurine tract preceeding the 3′-LTR and the 3′-LTR. (a) Four recombinant subgroups of sorghum CR5-Sb-[R1-R4] (i.e., R1–R4) are derived from sorghum CR5-Sb/CR6-Sb and rice CR5-Osj-A subfamilies. CR5-Osj-A was transferred to the sorghum genome via HT, where it recombined with CR5-Sb element to form CR5-Sb-R1 recombinants 1–4. CR5-Sb itself is thought to be a recombinant of CR6-Sb-A and a CR5-Sb progenitor that could not be detected. The oldest CR5-Sb-[R1-R4] member inserted 0.900 ± 0.116 Ma, and older members of parent CR5-Osj-A subfamily appear to have been lost from the sequenced Oryza sativa ssp. japonica genome. Only two young members of CR5-Osj-A family less than 0.026 ± 0.018 Ma could be detected in the current rice genome assembly. (b) Three recombinant subgroups of Setaria italica CR1-Si (R1, R1del, and R2) are derived from Se. italica CR1-Si-A and an O. minuta CR1-Om-like element (CR1-Si-B) that was transferred to the Se. italica genome via HT.