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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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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. |
format | Online Article Text |
id | pubmed-4627069 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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