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Characterisation of the Arabidopsis thaliana telomerase TERT-TR complex.
Stefanovie, Barbora; Jenner, Leon P; Bozdechová, Lucie; Fajkus, Petr; Sýkorová, Eva; Fajkus, Jirí; Palecek, Jan J.
Affiliation
  • Stefanovie B; Faculty of Science, National Centre for Biomolecular Research, Masaryk University, Kamenice 5, 62500, Brno, Czech Republic.
  • Jenner LP; Mendel Centre for Plant Genomics and Proteomics, Central European Institute of Technology, Masaryk University, Kamenice 5, 62500, Brno, Czech Republic.
  • Bozdechová L; Institute of Biophysics, The Czech Academy of Sciences, Kralovopolska 135, 61200, Brno, Czech Republic.
  • Fajkus P; Mendel Centre for Plant Genomics and Proteomics, Central European Institute of Technology, Masaryk University, Kamenice 5, 62500, Brno, Czech Republic.
  • Sýkorová E; Faculty of Science, National Centre for Biomolecular Research, Masaryk University, Kamenice 5, 62500, Brno, Czech Republic.
  • Fajkus J; Institute of Biophysics, The Czech Academy of Sciences, Kralovopolska 135, 61200, Brno, Czech Republic.
  • Palecek JJ; Institute of Biophysics, The Czech Academy of Sciences, Kralovopolska 135, 61200, Brno, Czech Republic.
Plant Mol Biol ; 114(3): 56, 2024 May 14.
Article in En | MEDLINE | ID: mdl-38743198
ABSTRACT
Most eukaryotic organisms employ a telomerase complex for the maintenance of chromosome ends. The core of this complex is composed of telomerase reverse transcriptase (TERT) and telomerase RNA (TR) subunits. The TERT reverse transcriptase (RT) domain synthesises telomeric DNA using the TR template sequence. The other TERT domains contribute to this process in different ways. In particular, the TERT RNA-binding domain (TRBD) interacts with specific TR motif(s). Using a yeast 3-hybrid system, we show the critical role of Arabidopsis thaliana (At) TRBD and embryophyta-conserved KRxR motif in the unstructured linker preceding the TRBD domain for binding to the recently identified AtTR subunit. We also show the essential role of the predicted P4 stem and pseudoknot AtTR structures and provide evidence for the binding of AtTRBD to pseudoknot and KRxR motif stabilising interaction with the P4 stem structure. Our results thus provide the first insight into the core part of the plant telomerase complex.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arabidopsis / Telomerase / Arabidopsis Proteins Language: En Journal: Plant Mol Biol / Plant mol. biol / Plant molecular biology Journal subject: BIOLOGIA MOLECULAR / BOTANICA Year: 2024 Type: Article Affiliation country: Czech Republic

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Arabidopsis / Telomerase / Arabidopsis Proteins Language: En Journal: Plant Mol Biol / Plant mol. biol / Plant molecular biology Journal subject: BIOLOGIA MOLECULAR / BOTANICA Year: 2024 Type: Article Affiliation country: Czech Republic