Searching journal content for articles similar to Woischnik and Moraes 12 (6): 885.

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  1. ..., Golovko G, Rojas M, Pavlidis I, Chumakov S, Aguilar G, Chávez A, Widger WR, et al. 2016. The ability of human nuclear DNA to cause false positive low-abundance heteroplasmy calls varies across the mitochondrial . BMC Genomics 17: 1017. doi:10.1186/s12864-016-3375-x ↵Barends M, Verschuren L, Morava E...
  2. ...of related species. Note that the gray branch is a separate background branch because it denotes the branch when the potential nuclear genomic integration took place.Selection analysis on isolated dcNUMT genes imply noncanonical NUMT integrations and “missing” mitochondrial sWe first conducted a codon...
  3. ...-coding genes, and StringTie transcriptsOf 19,972 nuclear protein-coding genes in N2 (WS292), 19,790 (99.1%) of N2 protein-coding genes encoded at least one unchanged product after mapping to CGC1. There were 46 protein-coding genes of N2 that, when lifted over to CGC1, overlapped AUGUSTUS predictions that also...
  4. ...kb mitochondrial , for which we obtained a complete and circularized sequence, whereas contigs 19–29 contain only 45S rDNA arrays. We found an enrichment of TTAGGG telomere repeats, typical of many eukaryotes, including true truffles (Martin et al. 2010), toward both ends of all 17 majors nuclear...
  5. ...in the assembly. As such, reads that would have mapped to ChrM mapped to the nuclear-embedded mitochondrial (NUMT) DNA sequences instead. In some cases, this would have resulted in Pilon editing the nuclear to match alleles found in the mitochondrial . These artifacts along with the other homozygous differences...
  6. ...ATP and ligating the cross-linked fragments to the blunt end. Proximal chromatin DNA was religated with the ligation enzyme. Nuclear complexes were reverse-cross-linked by incubation with Proteinase K at 65°C. DNA was purified by phenol–chloroform extraction. Biotin was removed from the ends of unligated fragments...
  7. ...interactions between mitochondrial (mtDNA)- and nuclear (nDNA)-encoded protein subunits. Although such interactions are fundamental to OXPHOS, bi-genomic coregulation is poorly understood. To address this question, we analyzed ∼8500 RNA-seq experiments from 48 human body sites. Despite well-known variation...
  8. ...in their nuclear organization and topological features, which prevented rediploidization, whereas sequence exchanges at LORe loci on other homeologs may have been locally maintained as a result of selection, for example by removing deleterious mutations or transferring favorable alleles at all gene loci...
  9. ...maps mitochondrial translationMitochondria have their own translation machinery to generate the 13 proteins encoded by the mitochondrial , which are all subunits of respiratory chain complexes (Pearce et al. 2017). As proteins composing the mitochondrial translation machinery are encoded by the nuclear...
  10. ...mitochondrial chromosomes in the absence of telomeric sequences (Supplemental Fig. S10). In addition, the presence of nonfunctional (and gradually degrading) nuclear copies of mtDNA (NUMTs) have previously been identified in H. vulgaris (Song et al. 2013). Sequence similarity searches did not detect NUMTs...
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