Histone H3 Variants in Trichomonas vaginalis
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
22408228
PubMed Central
PMC3346420
DOI
10.1128/ec.00006-12
PII: EC.00006-12
Knihovny.cz E-zdroje
- MeSH
- aktivace transkripce MeSH
- buněčné jádro genetika metabolismus MeSH
- centromera genetika metabolismus MeSH
- chromozomy genetika metabolismus MeSH
- fluorescenční mikroskopie MeSH
- G1 fáze MeSH
- G2 fáze MeSH
- genom protozoální * MeSH
- histony genetika metabolismus MeSH
- jaderný obal metabolismus MeSH
- mitóza MeSH
- molekulární sekvence - údaje MeSH
- nukleozomy metabolismus MeSH
- protozoální proteiny genetika metabolismus MeSH
- sekvence aminokyselin MeSH
- sekvenční analýza proteinů MeSH
- transformace genetická MeSH
- Trichomonas vaginalis genetika metabolismus MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- histony MeSH
- nukleozomy MeSH
- protozoální proteiny MeSH
The parabasalid protist Trichomonas vaginalis is a widespread parasite that affects humans, frequently causing vaginitis in infected women. Trichomonad mitosis is marked by the persistence of the nuclear membrane and the presence of an asymmetric extranuclear spindle with no obvious direct connection to the chromosomes. No centromeric markers have been described in T. vaginalis, which has prevented a detailed analysis of mitotic events in this organism. In other eukaryotes, nucleosomes of centromeric chromatin contain the histone H3 variant CenH3. The principal aim of this work was to identify a CenH3 homolog in T. vaginalis. We performed a screen of the T. vaginalis genome to retrieve sequences of canonical and variant H3 histones. Three variant histone H3 proteins were identified, and the subcellular localization of their epitope-tagged variants was determined. The localization of the variant TVAG_185390 could not be distinguished from that of the canonical H3 histone. The sequence of the variant TVAG_087830 closely resembled that of histone H3. The tagged protein colocalized with sites of active transcription, indicating that the variant TVAG_087830 represented H3.3 in T. vaginalis. The third H3 variant (TVAG_224460) was localized to 6 or 12 distinct spots at the periphery of the nucleus, corresponding to the number of chromosomes in G(1) phase and G(2) phase, respectively. We propose that this variant represents the centromeric marker CenH3 and thus can be employed as a tool to study mitosis in T. vaginalis. Furthermore, we suggest that the peripheral distribution of CenH3 within the nucleus results from the association of centromeres with the nuclear envelope throughout the cell cycle.
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