amazonensis (GenBank acc. no. EF559263); Lm, Selleckchem Mocetinostat L. major (TrEMBL acc. no. Q4QDR7); Li, L. infantum (GenBank acc. no. XP_001464939.1); Lb, L. brasiliensis (GenBank acc. no. XP_001564056.1); Tc, Trypanosoma cruzi (GenBank acc. no. XP_819954.1); Tb, Trypanosoma brucei (GenBank acc. no. AY910010); h, human (hTRF1 GenBank Acc. no. P54274.2; hTRF2 GenBank acc. no. Q15554). Figure 1 LaTRF is a homologue of mammalian and T. brucei telomeric TRFs.

(top) Position of the TRFH and Myb domains in LaTRF, according to rpsblast and bl2seq sequence analysis with T. brucei TRF. (bottom) ClustalW multiple alignment of the Myb-like DNA binding domains of human (hTRF2 and hTRF1), L. amazonensis (LaTRF), T. brucei (TbTRF) and T. cruzi (TcTRF) TRFs. In addition, like TbTRF, LaTRF shared sequence similarities with the canonical Myb-like domain and with the TRFH dimerization domain of human TRF1 and TRF2 (Fig 1-bottom and Table 1), but no sequence similarities were found with any other telobox PXD101 order protein (data not shown). Together, these results indicate that although LaTRF shares high sequence similarity with TbTRF, probably because the two species are phylogenetically related [26], further NVP-HSP990 studies are required

to confer any functions to the Leishmania TRF homologue identified here. LaTRF is a nuclear protein that co-localizes with L. amazonensis telomeres In exponentially growing L. amazonensis promastigotes, LaTRF was detected only in nuclear protein extracts. A single ~82.5 kDa protein band was selleck chemicals detected using anti-LaTRF serum (Fig 2 – top panel: lane 1). No protein was detected in cytoplasmic and total protein extracts (Fig 2 – top panel: lanes 2 and 3), indicating that LaTRF is a nuclear protein with very low intracellular abundance. As a control, Western blots were revealed with anti-LaRPA-1 serum, which recognizes a ~51.2 kDa telomeric protein band [23] (Fig 2 – bottom panel: lane 1) and also its phosphorylated forms (Fig 2 – bottom panel: lane 2; da Silveira & Cano, unpublished data). Figure 2 Expression of LaTRF in L. amazonensis promastigotes

extracts. Western blot analyses of extracts from 107 promastigotes/lane, grown in mid-log phase, were probed with anti-LaTRF serum (top panel) and anti-LaRPA-1 serum [31] as the loading control (bottom panel). Lane 1 – total protein extract (T), lane 2 – nuclear extract (N), lane 3 – cytoplasmic extract (C). We also developed an immunofluorescence assay combined with FISH, using anti-LaTRF serum and a PNA-telomere probe specific for TTAGGG repeats. As shown in Fig 3 (panels p1-4, merged images a and b), LaTRF is a nuclear protein that partially co-localizes with parasites telomeres, since some of the LaTRF signal coincided with telomeric foci and some did not (Fig 3, panels p1-4). In most cells, LaTRF appears as a diffuse signal spread all over the nucleoplasm and only in some cases it forms large punctuated foci, which seems to co-localize with the telomeric DNA (yellow dots in Fig 3, panels p2 and p4).