PubMed · 14478173
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T NAKAMURA. 1962. [Exercise load tests. In conclusion].. https://pubmed.ncbi.nlm.nih.gov/14478173/
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To determine the pathogenicities of mutated mtDNAs in patients with respiration defects, the possible involvement of nuclear DNA mutations has to be excluded, since respiratory function is controlled by both nuclear DNA and mtDNA. This was achieved by showing that the mutated mtDNAs and respiration defects were co-transferred from patients to mtDNA-less human cells, and the resultant cybrid clones carrying mutated mtDNAs expressed respiration defects. To decide whether the cybrid clones expressed respiration defects, in this study the lowest limits of normal respiratory function were evaluated by transfer of mtDNAs from 54 normal subjects to mtDNA-less HeLa cells. The resultant cybrid clones showed that 71% respiratory function was the lowest limit of mtDNAs from normal subjects. On the other hand, cybrid clones carrying pathogenic mtDNAs from patients with mitochondrial diseases showed 0-64% respiratory function, suggesting that less than 71% respiratory function in cybrid clones should be a reliable indicator of whether the mutated mtDNAs of the patients were pathogenic.
Current regional estimates of net primary productivity (NPP) of boreal black spruce overlook the large variation in NPP caused by small-scale topographic effects on soil water, temperature and nutrient availability. Topographic effects on black spruce NPP could likely be modeled by simulating the lateral and vertical movement of water, and its effects on soil nutrient transformation and uptake, through three-dimensional watersheds defined by aspects and slopes of their topographic positions. To examine this likelihood, the ecosystem model 'ecosys' was run for 120 years on a transect that included upper- and lower-slope positions and a basin in which a basal water table was set 0.5 m below the soil surface. For the run, we used soil properties and weather conditions recorded at the 115-year-old BOREAS Southern Old Black Spruce site. Short-term model performance was tested by comparing diurnal and annual carbon (C) transfers simulated under 1994 weather conditions during the 115th year of the model run with those measured at this site during 1994 by eddy covariance, surface chambers and allometry. After 115 years, annual spruce NPP simulated at the upper-slope positions was twice that at the basin (350 versus 170 g C m-2), whereas accumulated wood C was almost three times as large (6.8 versus 2.4 kg C m-2). In the model, increases in NPP and wood growth in upper-slope positions were caused by lower soil water contents, higher soil temperatures, and more rapid O2 uptake that accelerated heterotrophic respiration and hence nutrient mineralization and uptake. Modeled differences in wood growth with topographic position were quantitatively consistent with measurements of boreal black spruce at several research sites differing in water table depth. Modeled differences also agreed with differences in wood growth rates derived from allometric measurements at boreal black spruce sites differing in productivity indices as a result of differences in subsurface hydrology. The magnitude of these differences clearly indicates the importance of accounting for subsurface hydrology in regional estimates of boreal forest productivity.
Cytochrome c peroxidase (CcP) uses hydrogen peroxide as an electron acceptor to oxidize cytochrome c (Cc) in the mitochondrial intermembrane space. A null allele of yeast CCP1 gene encoding CcP was created by one-step gene disruption method in a diploid yeast strain. Haploid yeast cells with the disrupted CCP1 gene were viable and able to grow in a medium containing lactic acid or glycerol as an energy source, indicating that CcP is not essential for both cell viability and respiration. However, CCP1-disrupted cells were more sensitive to H2O2 than wild-type cells. We also constructed a CCP1-lacZ fused gene and integrated this gene into yeast chromosomal DNA to monitor the expression of CCP1 gene. We found that expression of CCP1 gene increases under respiratory culture conditions and by treatments with H2O2. These results hint that the biological function of CcP is to reduce H2O2 generated during aerobic respiratory process. Moreover, expression of CCP1 gene increased by treatments with peroxynitrite, indicating that CcP may act as a peroxynitrite scavenger.