Details

Autor(en) / Beteiligte

• Fernandes, Carlos A.H.
• Morea, Edna Gicela O.
• dos Santos, Gabriel A.
• da Silva, Vitor L.
• Vieira, Marina Roveri
• Viviescas, Maria Alejandra
• Chatain, Jean
• Vadel, Aurélie
• Saintomé, Carole
• Fontes, Marcos Roberto M.
• Cano, Maria Isabel Nogueira

Titel

A multi-approach analysis highlights the relevance of RPA-1 as a telomere end-binding protein (TEBP) in Leishmania amazonensis

Ist Teil von

• Biochimica et biophysica acta. General subjects, 2020-07, Vol.1864 (7), p.129607-129607, Article 129607

Ort / Verlag

Netherlands: Elsevier B.V

Erscheinungsjahr

2020

Link zum Volltext

Quelle

Alma/SFX Local Collection

Beschreibungen/Notizen

• Telomeres are chromosome end structures important in the maintenance of genome homeostasis. They are replenished by the action of telomerase and associated proteins, such as the OB (oligonucleotide/oligosaccharide-binding)-fold containing telomere-end binding proteins (TEBP) which plays an essential role in telomere maintenance and protection. The nature of TEBPs is well known in higher and some primitive eukaryotes, but it remains undetermined in trypanosomatids. Previous in silico searches have shown that there are no homologs of the classical TEPBs in trypanosomatids, including Leishmania sp. However, Replication Protein A subunit 1 (RPA-1), an OB-fold containing DNA-binding protein, was found co-localized with trypanosomatids telomeres and showed a high preference for the telomeric G-rich strand. We predicted the absence of structural homologs of OB-fold containing TEBPs in the Leishmania sp. genome using structural comparisons. We demonstrated by molecular docking that the ssDNA binding mode of LaRPA-1 shares features with the higher eukaryotes POT1 and RPA-1 crystal structures ssDNA binding mode. Using fluorescence spectroscopy, protein-DNA interaction assays, and FRET, we respectively show that LaRPA-1 shares some telomeric functions with the classical TEBPs since it can bind at least one telomeric repeat, protect the telomeric G-rich DNA from 3′-5′ Exonuclease I digestion, and unfold telomeric G-quadruplex. Our results suggest that RPA-1 emerges as a TEBP in trypanosomatids, and in this context, we present two possible evolutionary landscapes of trypanosomatids RPA-1 that could reflect upon the evolution of OB-fold containing TEBPs from all eukaryotes. [Display omitted] •Trypanosomatids do not present classical OB-fold containing telomeric proteins.•LaRPA-1/ssDNA binding mode is similar to POT1 and RPA-1 from higher eukaryotes.•LaRPA-1 has protective telomeric functions against 3′-5′ exonucleolytic activity.•LaRPA-1 can unfold G-quadruplex structures similar to POT1, CST and heterotrimeric RPA.•Two possible evolutionary landscapes of trypanosomatids RPA-1 could reflect upon the evolution of TEBPs.