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9103 - 12977 Mus Musculus - Deletions Deletion length: 3873 bp |
Breakpoint flanking sequences more information in Documentation - Flanking regions |
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Two-dimensional scatterplot showing the location of the selected deletion (red diamond) versus the full dataset (grey dots). Each point represents an mtDNA rearrangement with the 5’ breakpoint on the x-axis and the 3’ breakpoint on the y-axis. |
Circular mtDNA plot specifying the location of the deleted region (black bar). |
Length distribution of the deleted region in the selected deletion (red bar) versus the full dataset (grey bars) .The cases were grouped 100-nt windows. |
References
[2] Tanhauser, S. M., Laipis, P. J., Multiple deletions are detectable in mitochondrial DNA of aging mice.The Journal of Biological Chemistry. 1995. 270(42): p. 24769-75.
[4] Chung, S. S., et al., Analysis of age-associated mitochondrial DNA deletion breakpoint regions from mice suggests a novel model of deletion formation.Age. 1996. 19(4): p. 117-128.
[5] Wang, E., et al., The rate of mitochondrial mutagenesis is faster in mice than humans.Mutation Research. 1997. 377(2): p. 157-66.
[8] Fujibayashi, Y., et al., Increased mitochondrial DNA deletion in the brain of SAMP8, a mouse model for spontaneous oxidative stress barin.Neuroscience Letters. 1998. 254(2): p. 109-12.
[14] Vermulst, M., et al., DNA deletions and clonal mutations drive premature aging in mitochondrial mutator mice.Nature Genetics. 2008. 40(4): p. 392-4.
[18] Brossas, J. Y., et al., Multiple deletions in mitochondrial DNA are present in senescent mouse brain.Biochemical and Biophysical Research Communications. 1994. 202(2): p. 654-9.
[21] Zeng, Z., et al., Mitochondrial DNA deletions are associated with ischemia and aging in Balb/c mouse brain.Journal of Cellular Biochemistry. 1999. 73(4): p. 545-53.
[22] Zhang, W., et al., Mediating effect of ROS on mtDNA damage and low ATP content induced by arsenic trioxide in mouse oocytes.Toxicology in Vitro. 2011. 25(4): p. 979-84.
[23] Kronenberg, G., et al., Folate deficiency increases mtDNA and D-1 mtDNa deletion in aged brain of mice lacking uracil-DNA glycosylase.Experimental Neurology. 2011. 228(2): p. 253-8.