Fig. 2.
Presence–absence analyses of SINE integrations. The multilocus markers were detected by Southern blot hybridization with the strepsirrhine-specific Alu probe (A) and the lorisiform-specific tRNA-derived SINE probe (B) are shown. PCR amplification of the Che1 monolocus marker (C) and its schematic presentation (D) are shown. (E) Phylogenetic relationships among analyzed strepsirrhine genera as obtained from SINE integrations, with squares and circles indicating multi- and monolocus markers, respectively. ATR, Allocebus trichotis; CGU, Colobus guereza; CJA, Callithrix jacchus; CME, Cheirogaleus medius; DMA, Daubentonia madagascariensis; DR, direct repeats; GMO, Galago moholi; LCA, Lemur catta; LRU, Lepilemur ruficaudatus; LTA, Loris tardigradus; MCO, Mirza coquereli; MMU, Microcebus murinus; NBE, Nycticebus bengalensis; OCR, Otolemur crassicaudatus; PFU, Phaner furcifer; PPO, Perodicticus potto; PVE, Propithecus verreauxi; St, standard (see also supporting information).