Cargando…

A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution

Telomere loops (t-loops) are formed at the ends of chromosomes in species ranging from humans to worms, plants, and with genetic manipulation, some yeast. Recent in vitro studies demonstrated that transcription of telomeric DNA leads to highly efficient t-loop formation. It was also shown that both...

Descripción completa

Detalles Bibliográficos
Autores principales: Tomaska, Lubomir, Nosek, Jozef, Kar, Anirban, Willcox, Smaranda, Griffith, Jack D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702307/
https://www.ncbi.nlm.nih.gov/pubmed/31475042
http://dx.doi.org/10.3389/fgene.2019.00792
_version_ 1783445201422909440
author Tomaska, Lubomir
Nosek, Jozef
Kar, Anirban
Willcox, Smaranda
Griffith, Jack D.
author_facet Tomaska, Lubomir
Nosek, Jozef
Kar, Anirban
Willcox, Smaranda
Griffith, Jack D.
author_sort Tomaska, Lubomir
collection PubMed
description Telomere loops (t-loops) are formed at the ends of chromosomes in species ranging from humans to worms, plants, and with genetic manipulation, some yeast. Recent in vitro studies demonstrated that transcription of telomeric DNA leads to highly efficient t-loop formation. It was also shown that both DNA termini are inserted into the preceding DNA to generate a highly stable t-loop junction. Furthermore, some telomeric RNA remains present at the junction, potentially acting as a plug to further protect and stabilize the t-loop. Modeling the loop junction reveals two mechanisms by which the canonical chromosomal replication factors could extend the telomere in the absence of telomerase. One mechanism would utilize the annealed 3’ terminus as a de novo replication origin. In vitro evidence for the ability of the t-loop to prime telomere extension using the T7 replication factors is presented. A second mechanism would involve resolution of the Holliday junction present in the t-loop bubble by factors such as GEN1 to generate a rolling circle template at the extreme terminus of the telomere. This could lead to large expansions of the telomeric tract. Here, we propose that telomeres evolved as terminal elements containing long arrays of short nucleotide repeats due to the ability of such arrays to fold back into loops and self-prime their replicative extension. In this view, telomerase may have evolved later to provide a more precise mechanism of telomere maintenance. Both pathways have direct relevance to the alternative lengthening of telomeres (ALT) pathway. This view also provides a possible mechanism for the very large repeat expansions observed in nucleotide repeat diseases such as Fragile X syndrome, myotonic dystrophy, familial amyotrophic lateral sclerosis (ALS), and frontotemporal dementia (FTD). The evolution of telomeres is discussed in the framework of these models.
format Online
Article
Text
id pubmed-6702307
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-67023072019-08-30 A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution Tomaska, Lubomir Nosek, Jozef Kar, Anirban Willcox, Smaranda Griffith, Jack D. Front Genet Genetics Telomere loops (t-loops) are formed at the ends of chromosomes in species ranging from humans to worms, plants, and with genetic manipulation, some yeast. Recent in vitro studies demonstrated that transcription of telomeric DNA leads to highly efficient t-loop formation. It was also shown that both DNA termini are inserted into the preceding DNA to generate a highly stable t-loop junction. Furthermore, some telomeric RNA remains present at the junction, potentially acting as a plug to further protect and stabilize the t-loop. Modeling the loop junction reveals two mechanisms by which the canonical chromosomal replication factors could extend the telomere in the absence of telomerase. One mechanism would utilize the annealed 3’ terminus as a de novo replication origin. In vitro evidence for the ability of the t-loop to prime telomere extension using the T7 replication factors is presented. A second mechanism would involve resolution of the Holliday junction present in the t-loop bubble by factors such as GEN1 to generate a rolling circle template at the extreme terminus of the telomere. This could lead to large expansions of the telomeric tract. Here, we propose that telomeres evolved as terminal elements containing long arrays of short nucleotide repeats due to the ability of such arrays to fold back into loops and self-prime their replicative extension. In this view, telomerase may have evolved later to provide a more precise mechanism of telomere maintenance. Both pathways have direct relevance to the alternative lengthening of telomeres (ALT) pathway. This view also provides a possible mechanism for the very large repeat expansions observed in nucleotide repeat diseases such as Fragile X syndrome, myotonic dystrophy, familial amyotrophic lateral sclerosis (ALS), and frontotemporal dementia (FTD). The evolution of telomeres is discussed in the framework of these models. Frontiers Media S.A. 2019-08-14 /pmc/articles/PMC6702307/ /pubmed/31475042 http://dx.doi.org/10.3389/fgene.2019.00792 Text en Copyright © 2019 Tomaska, Nosek, Kar, Willcox and Griffith http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Tomaska, Lubomir
Nosek, Jozef
Kar, Anirban
Willcox, Smaranda
Griffith, Jack D.
A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution
title A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution
title_full A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution
title_fullStr A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution
title_full_unstemmed A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution
title_short A New View of the T-Loop Junction: Implications for Self-Primed Telomere Extension, Expansion of Disease-Related Nucleotide Repeat Blocks, and Telomere Evolution
title_sort new view of the t-loop junction: implications for self-primed telomere extension, expansion of disease-related nucleotide repeat blocks, and telomere evolution
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6702307/
https://www.ncbi.nlm.nih.gov/pubmed/31475042
http://dx.doi.org/10.3389/fgene.2019.00792
work_keys_str_mv AT tomaskalubomir anewviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT nosekjozef anewviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT karanirban anewviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT willcoxsmaranda anewviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT griffithjackd anewviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT tomaskalubomir newviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT nosekjozef newviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT karanirban newviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT willcoxsmaranda newviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution
AT griffithjackd newviewofthetloopjunctionimplicationsforselfprimedtelomereextensionexpansionofdiseaserelatednucleotiderepeatblocksandtelomereevolution