scholarly journals Exposure to environmental radionuclides alters mitochondrial DNA maintenance in a wild rodent

2020 ◽  
Vol 34 (2) ◽  
pp. 163-174 ◽  
Author(s):  
Jenni Kesäniemi ◽  
Anton Lavrinienko ◽  
Eugene Tukalenko ◽  
Ana Filipa Moutinho ◽  
Tapio Mappes ◽  
...  
2011 ◽  
Vol 39 (12) ◽  
pp. 5098-5108 ◽  
Author(s):  
A. Reyes ◽  
J. He ◽  
C. C. Mao ◽  
L. J. Bailey ◽  
M. Di Re ◽  
...  

2016 ◽  
Vol 1857 ◽  
pp. e27
Author(s):  
Eduardo Silva Ramos ◽  
Elisa Motori ◽  
Christian Brüser ◽  
Inge Kühl ◽  
Benedetta Ruzzenente ◽  
...  

2019 ◽  
Vol 97 (2) ◽  
pp. 276-286
Author(s):  
Ewen W. Sommerville ◽  
Ilaria Dalla Rosa ◽  
Masha M. Rosenberg ◽  
Francesco Bruni ◽  
Kyle Thompson ◽  
...  

Brain ◽  
2014 ◽  
Vol 137 (5) ◽  
pp. 1323-1336 ◽  
Author(s):  
Gerald Pfeffer ◽  
Gráinne S Gorman ◽  
Helen Griffin ◽  
Marzena Kurzawa-Akanbi ◽  
Emma L. Blakely ◽  
...  

mBio ◽  
2015 ◽  
Vol 6 (1) ◽  
Author(s):  
Jiří Týč ◽  
Michele M. Klingbeil ◽  
Julius Lukeš

ABSTRACT  Mitochondrial chaperones have multiple functions that are essential for proper functioning of mitochondria. In the human-pathogenic protist Trypanosoma brucei, we demonstrate a novel function of the highly conserved machinery composed of mitochondrial heat shock proteins 70 and 40 (mtHsp70/mtHsp40) and the ATP exchange factor Mge1. The mitochondrial DNA of T. brucei, also known as kinetoplast DNA (kDNA), is represented by a single catenated network composed of thousands of minicircles and dozens of maxicircles packed into an electron-dense kDNA disk. The chaperones mtHsp70 and mtHsp40 and their cofactor Mge1 are uniformly distributed throughout the single mitochondrial network and are all essential for the parasite. Following RNA interference (RNAi)-mediated depletion of each of these proteins, the kDNA network shrinks and eventually disappears. Ultrastructural analysis of cells depleted for mtHsp70 or mtHsp40 revealed that the otherwise compact kDNA network becomes severely compromised, a consequence of decreased maxicircle and minicircle copy numbers. Moreover, we show that the replication of minicircles is impaired, although the lack of these proteins has a bigger impact on the less abundant maxicircles. We provide additional evidence that these chaperones are indispensable for the maintenance and replication of kDNA, in addition to their already known functions in Fe-S cluster synthesis and protein import. IMPORTANCE  Impairment or loss of mitochondrial DNA is associated with mitochondrial dysfunction and a wide range of neural, muscular, and other diseases. We present the first evidence showing that the entire mtHsp70/mtHsp40 machinery plays an important role in mitochondrial DNA replication and maintenance, a function likely retained from prokaryotes. These abundant, ubiquitous, and multifunctional chaperones share phenotypes with enzymes engaged in the initial stages of replication of the mitochondrial DNA in T. brucei.


2009 ◽  
Vol 29 (15) ◽  
pp. 4274-4282 ◽  
Author(s):  
Julien P. Duxin ◽  
Benjamin Dao ◽  
Peter Martinsson ◽  
Nina Rajala ◽  
Lionel Guittat ◽  
...  

ABSTRACT Dna2 is a highly conserved helicase/nuclease that in yeast participates in Okazaki fragment processing, DNA repair, and telomere maintenance. Here, we investigated the biological function of human Dna2 (hDna2). Immunofluorescence and biochemical fractionation studies demonstrated that hDna2 was present in both the nucleus and the mitochondria. Analysis of mitochondrial hDna2 revealed that it colocalized with a subfraction of DNA-containing mitochondrial nucleoids in unperturbed cells. Upon the expression of disease-associated mutant forms of the mitochondrial Twinkle helicase which induce DNA replication pausing/stalling, hDna2 accumulated within nucleoids. RNA interference-mediated depletion of hDna2 led to a modest decrease in mitochondrial DNA replication intermediates and inefficient repair of damaged mitochondrial DNA. Importantly, hDna2 depletion also resulted in the appearance of aneuploid cells and the formation of internuclear chromatin bridges, indicating that nuclear hDna2 plays a role in genomic DNA stability. Together, our data indicate that hDna2 is similar to its yeast counterpart and is a new addition to the growing list of proteins that participate in both nuclear and mitochondrial DNA maintenance.


Mitochondrion ◽  
2007 ◽  
Vol 7 (6) ◽  
pp. 414
Author(s):  
Matthew J. Young ◽  
Deborah A. Court

2015 ◽  
Vol 112 (30) ◽  
pp. 9334-9339 ◽  
Author(s):  
J. Bradley Holmes ◽  
Gokhan Akman ◽  
Stuart R. Wood ◽  
Kiran Sakhuja ◽  
Susana M. Cerritelli ◽  
...  

Encoding ribonuclease H1 (RNase H1) degrades RNA hybridized to DNA, and its function is essential for mitochondrial DNA maintenance in the developing mouse. Here we define the role of RNase H1 in mitochondrial DNA replication. Analysis of replicating mitochondrial DNA in embryonic fibroblasts lacking RNase H1 reveals retention of three primers in the major noncoding region (NCR) and one at the prominent lagging-strand initiation site termed Ori-L. Primer retention does not lead immediately to depletion, as the persistent RNA is fully incorporated in mitochondrial DNA. However, the retained primers present an obstacle to the mitochondrial DNA polymerase γ in subsequent rounds of replication and lead to the catastrophic generation of a double-strand break at the origin when the resulting gapped molecules are copied. Hence, the essential role of RNase H1 in mitochondrial DNA replication is the removal of primers at the origin of replication.


2020 ◽  
Vol 131 (4) ◽  
pp. e179
Author(s):  
D. Lehmann ◽  
H. Rosa ◽  
M. Rocha ◽  
S. Zierz ◽  
R.W. Taylor ◽  
...  

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