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Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element

The majority of mitochondrial DNA replication events are terminated prematurely. The nascent DNA remains stably associated with the template, forming a triple-stranded displacement loop (D-loop) structure. However, the function of the D-loop region of the mitochondrial genome remains poorly understo...

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Autores principales: Jemt, Elisabeth, Persson, Örjan, Shi, Yonghong, Mehmedovic, Majda, Uhler, Jay P., Dávila López, Marcela, Freyer, Christoph, Gustafsson, Claes M., Samuelsson, Tore, Falkenberg, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627069/
https://www.ncbi.nlm.nih.gov/pubmed/26253742
http://dx.doi.org/10.1093/nar/gkv804
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author Jemt, Elisabeth
Persson, Örjan
Shi, Yonghong
Mehmedovic, Majda
Uhler, Jay P.
Dávila López, Marcela
Freyer, Christoph
Gustafsson, Claes M.
Samuelsson, Tore
Falkenberg, Maria
author_facet Jemt, Elisabeth
Persson, Örjan
Shi, Yonghong
Mehmedovic, Majda
Uhler, Jay P.
Dávila López, Marcela
Freyer, Christoph
Gustafsson, Claes M.
Samuelsson, Tore
Falkenberg, Maria
author_sort Jemt, Elisabeth
collection PubMed
description The majority of mitochondrial DNA replication events are terminated prematurely. The nascent DNA remains stably associated with the template, forming a triple-stranded displacement loop (D-loop) structure. However, the function of the D-loop region of the mitochondrial genome remains poorly understood. Using a comparative genomics approach we here identify two closely related 15 nt sequence motifs of the D-loop, strongly conserved among vertebrates. One motif is at the D-loop 5′-end and is part of the conserved sequence block 1 (CSB1). The other motif, here denoted coreTAS, is at the D-loop 3′-end. Both these sequences may prevent transcription across the D-loop region, since light and heavy strand transcription is terminated at CSB1 and coreTAS, respectively. Interestingly, the replication of the nascent D-loop strand, occurring in a direction opposite to that of heavy strand transcription, is also terminated at coreTAS, suggesting that coreTAS is involved in termination of both transcription and replication. Finally, we demonstrate that the loading of the helicase TWINKLE at coreTAS is reversible, implying that this site is a crucial component of a switch between D-loop formation and full-length mitochondrial DNA replication.
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spelling pubmed-46270692015-11-13 Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element Jemt, Elisabeth Persson, Örjan Shi, Yonghong Mehmedovic, Majda Uhler, Jay P. Dávila López, Marcela Freyer, Christoph Gustafsson, Claes M. Samuelsson, Tore Falkenberg, Maria Nucleic Acids Res Genome Integrity, Repair and Replication The majority of mitochondrial DNA replication events are terminated prematurely. The nascent DNA remains stably associated with the template, forming a triple-stranded displacement loop (D-loop) structure. However, the function of the D-loop region of the mitochondrial genome remains poorly understood. Using a comparative genomics approach we here identify two closely related 15 nt sequence motifs of the D-loop, strongly conserved among vertebrates. One motif is at the D-loop 5′-end and is part of the conserved sequence block 1 (CSB1). The other motif, here denoted coreTAS, is at the D-loop 3′-end. Both these sequences may prevent transcription across the D-loop region, since light and heavy strand transcription is terminated at CSB1 and coreTAS, respectively. Interestingly, the replication of the nascent D-loop strand, occurring in a direction opposite to that of heavy strand transcription, is also terminated at coreTAS, suggesting that coreTAS is involved in termination of both transcription and replication. Finally, we demonstrate that the loading of the helicase TWINKLE at coreTAS is reversible, implying that this site is a crucial component of a switch between D-loop formation and full-length mitochondrial DNA replication. Oxford University Press 2015-10-30 2015-08-07 /pmc/articles/PMC4627069/ /pubmed/26253742 http://dx.doi.org/10.1093/nar/gkv804 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genome Integrity, Repair and Replication
Jemt, Elisabeth
Persson, Örjan
Shi, Yonghong
Mehmedovic, Majda
Uhler, Jay P.
Dávila López, Marcela
Freyer, Christoph
Gustafsson, Claes M.
Samuelsson, Tore
Falkenberg, Maria
Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element
title Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element
title_full Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element
title_fullStr Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element
title_full_unstemmed Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element
title_short Regulation of DNA replication at the end of the mitochondrial D-loop involves the helicase TWINKLE and a conserved sequence element
title_sort regulation of dna replication at the end of the mitochondrial d-loop involves the helicase twinkle and a conserved sequence element
topic Genome Integrity, Repair and Replication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4627069/
https://www.ncbi.nlm.nih.gov/pubmed/26253742
http://dx.doi.org/10.1093/nar/gkv804
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