TY - JOUR
T1 - Increased negative supercoiling of mtDNA in TOP1mt knockout mice and presence of topoisomerases IIα and IIβ in vertebrate mitochondria
AU - Zhang, Hongliang
AU - Zhang, Yong Wei
AU - Yasukawa, Takehiro
AU - Dalla Rosa, Ilaria
AU - Khiati, Salim
AU - Pommier, Yves
N1 - Funding Information:
NIH Intramural Program, Center for Cancer Research, National Cancer Institute [Z01 BC 006161]; Biotechnol- ogy and Biological Sciences Research Council (UK) David Phillips Fellowship (to T.Y.). Funding for open access charge: NIH Intramural Program, Center for Cancer Research, National Cancer Institute [Z01 BC 006161]. Conflict of interest statement. None declared.
PY - 2014/6/17
Y1 - 2014/6/17
N2 - Topoisomerases are critical for replication, DNA packing and repair, as well as for transcription by allowing changes in DNA topology. Cellular DNA is present both in nuclei and mitochondria, and mitochondrial topoisomerase I (Top1mt) is the only DNA topoisomerase specific for mitochondria in vertebrates. Here, we report in detail the generation of TOP1mt knockout mice, and demonstrate that mitochondrial DNA (mtDNA) displays increased negative supercoiling in TOP1mt knockout cells and murine tissues. This finding suggested imbalanced topoisomerase activity in the absence of Top1mt and the activity of other topoisomerases in mitochondria. Accordingly, we found that both Top2α and Top2β are present and active in mouse and human mitochondria. The presence of Top2α-DNA complexes in the mtDNA D-loop region, at the sites where both ends of 7S DNA are positioned, suggests a structural role for Top2 in addition to its classical topoisomerase activities.
AB - Topoisomerases are critical for replication, DNA packing and repair, as well as for transcription by allowing changes in DNA topology. Cellular DNA is present both in nuclei and mitochondria, and mitochondrial topoisomerase I (Top1mt) is the only DNA topoisomerase specific for mitochondria in vertebrates. Here, we report in detail the generation of TOP1mt knockout mice, and demonstrate that mitochondrial DNA (mtDNA) displays increased negative supercoiling in TOP1mt knockout cells and murine tissues. This finding suggested imbalanced topoisomerase activity in the absence of Top1mt and the activity of other topoisomerases in mitochondria. Accordingly, we found that both Top2α and Top2β are present and active in mouse and human mitochondria. The presence of Top2α-DNA complexes in the mtDNA D-loop region, at the sites where both ends of 7S DNA are positioned, suggests a structural role for Top2 in addition to its classical topoisomerase activities.
UR - http://www.scopus.com/inward/record.url?scp=84903120104&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84903120104&partnerID=8YFLogxK
U2 - 10.1093/nar/gku384
DO - 10.1093/nar/gku384
M3 - Article
C2 - 24803675
AN - SCOPUS:84903120104
SN - 0305-1048
VL - 42
SP - 7259
EP - 7267
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 11
ER -