860 research outputs found
Knockout of the US29 Gene of Human Cytomegalovirus Using BAC Recombineering
Color poster with text, diagrams, images, and charts.The purpose of this study was to determine the function of the US29 gene in Human Cytomegalovirus (HCMV) by knocking it out using Bacterial Artificial Chromosome (BAC) technology.University of Wisconsin--Eau Claire Office of Research and Sponsored Programs
Coal-packed methane biofilter for mitigation of green house gas emissions from coal mine ventilation air
Methane emitted by coal mine ventilation air (MVA) is a significant greenhouse gas. A mitigation strategy is the oxidation of methane to carbon dioxide, which is approximately twenty-one times less effective at global warming than methane on a mass-basis. The low non-combustible methane concentrations at high MVA flow rates call for a catalytic strategy of oxidation. A laboratory-scale coal-packed biofilter was designed and partially removed methane from humidified air at flow rates between 0.2 and 2.4 L min -1 at 30°C with nutrient solution added every three days. Methane oxidation was catalysed by a complex community of naturally-occurring microorganisms, with the most abundant member being identified by 16S rRNA gene sequence as belonging to the methanotrophic genus Methylocystis. Additional inoculation with a laboratorygrown culture of Methylosinus sporium, as investigated in a parallel run, only enhanced methane consumption during the initial 12 weeks. The greatest level of methane removal of 27.260.66 g methane m23 empty bed h21 was attained for the non-inoculated system, which was equivalent to removing 19.762.9% methane from an inlet concentration of 1% v/v at an inlet gas flow rate of 1.6 L min21 (2.4 min empty bed residence time). These results show that low-cost coal packing holds promising potential as a suitable growth surface and contains methanotrophic microorganisms for the catalytic oxidative removal of methane.©2014 Limbri et al
Use of high throughput sequencing to observe genome dynamics at a single cell level
With the development of high throughput sequencing technology, it becomes
possible to directly analyze mutation distribution in a genome-wide fashion,
dissociating mutation rate measurements from the traditional underlying
assumptions. Here, we sequenced several genomes of Escherichia coli from
colonies obtained after chemical mutagenesis and observed a strikingly
nonrandom distribution of the induced mutations. These include long stretches
of exclusively G to A or C to T transitions along the genome and orders of
magnitude intra- and inter-genomic differences in mutation density. Whereas
most of these observations can be explained by the known features of enzymatic
processes, the others could reflect stochasticity in the molecular processes at
the single-cell level. Our results demonstrate how analysis of the molecular
records left in the genomes of the descendants of an individual mutagenized
cell allows for genome-scale observations of fixation and segregation of
mutations, as well as recombination events, in the single genome of their
progenitor.Comment: 22 pages, 9 figures (including 5 supplementary), one tabl
Infection with Salmonella enterica Serovar Typhimurium Leads to Increased Proportions of F4/80+ Red Pulp Macrophages and Decreased Proportions of B and T Lymphocytes in the Spleen.
Infection of mice with Salmonella enterica serovar Typhimurium (Salmonella) causes systemic inflammatory disease and enlargement of the spleen (splenomegaly). Splenomegaly has been attributed to a general increase in the numbers of phagocytes, lymphocytes, as well as to the expansion of immature CD71+Ter119+ reticulocytes. The spleen is important for recycling senescent red blood cells (RBCs) and for the capture and eradication of blood-borne pathogens. Conservation of splenic tissue architecture, comprised of the white pulp (WP), marginal zone (MZ), and red pulp (RP) is essential for initiation of adaptive immune responses to captured pathogens. Using flow cytometry and four color immunofluorescence microscopy (IFM), we show that Salmonella-induced splenomegaly is characterized by drastic alterations of the splenic tissue architecture and cell population proportions, as well as in situ cell distributions. A major cause of splenomegaly appears to be the significant increase in immature RBC precursors and F4/80+ macrophages that are important for recycling of heme-associated iron. In contrast, the proportions of B220+, CD4+ and CD8+ lymphocytes, as well as MZ MOMA+ macrophages decrease significantly as infection progresses. Spleen tissue sections show visible tears and significantly altered tissue architecture with F4/80+ macrophages and RBCs expanding beyond the RP and taking over most of the spleen tissue. Additionally, F4/80+ macrophages actively phagocytose not only RBCs, but also lymphocytes, indicating that they may contribute to declining lymphocyte proportions during Salmonella infection. Understanding how these alterations of spleen microarchitecture impact the generation of adaptive immune responses to Salmonella has implications for understanding Salmonella pathogenesis and for the design of more effective Salmonella-based vaccines
The Giving Trees: The (Un)Sustainability of Palm Oil in Indonesia
Palm oil is the main source of cooking oil for much of Africa, Asia and Brazil. Due to the increasingly high demand for palm oil, countries such as Indonesia and Malaysia have cleared millions of acres of tropical rainforests to create space for oil palm plantations. This deforestation has led to extreme environmental and social concerns such as the burning of peatlands, the endangerment of a number of species, including the Sumatran Tiger, rhinos and orangutans, and the displacement of native populations. Indonesia is the world’s largest consumer and producer of palm oil, producing almost half of the world’s supply which has created a dependence on palm oil for the success of their economy. This has created an economics-ecology dilemma for the country, yet, still, the success of their economy is dependent on the sustainability of their environment. There have been a number of international efforts to improve the sustainability of the industry, but there has been no lasting change as the attraction to profits has greatly outweighed the negative implications of growth. The environmental impacts of the industry raise serious concerns for the survival of these rich and vital rainforests. In his book, Loving Nature, James A. Nash discusses a number of theological arguments for ecology that are can be directly applied to the palm oil industry of Indonesia. Christians, Nash discusses, are called to love thy neighbor, which must include non-human neighbors. Christians also have the responsibility to care for future generations, which entails preserving the natural resources of our planet. The social and ecological effects of the Indonesian palm oil industry violate the integrity of the planet, our neighbors, and future generations, and is thus violating Christian ecological responsibility
Another Description of Ross\u27 Gull
One immature was observed at Sutherland Reservoir, Lincoln County, on 17 December (myself) and 19 December (myself and Dorothy J. Rosche), 1992. I saw this bird a few hours after Silcock and Dinsmore discovered it on 17 Dec. [See article on p. 88.] It flew by the end of the pier at close distances (as close as 20 feet) for hours on both days of observation. It sometimes landed momentarily on small pieces of ice as it picked up morsels floating in the water. It was a small gull and much more dainty than the nearby Bonaparte\u27s Gulls. It had a very small, rounded head and a very short, stubby, blackish bill. I believe it was a first-year bird molting into second-year plumage. The obviously wedge-shaped tail possessed well-worn tips. The only thing left of the dark tail band was a dark spot or two. The dark wing band of the immature was reduced to a short, dark bar on the inner wing, more noticeable on one side of the bird than the other (and very visible when the bird perched). The dark black collar marking was just beginning to appear, a small, darkish line being the only thing visible on each side of the head at this time. The pointed wings were rather uniformly gray on both sides; the trailing edge of the wing was whitish. The bird remained until 3 January, 1993, when it was last seen at the inlet to the reservoir. I personally visited with some 18 people who travelled to observe the bird from New York, Massachusetts, New Jersey, Colorado, and Florida
Phenotypic landscape inference reveals multiple evolutionary paths to C photosynthesis
C photosynthesis has independently evolved from the ancestral C
pathway in at least 60 plant lineages, but, as with other complex traits, how
it evolved is unclear. Here we show that the polyphyletic appearance of C
photosynthesis is associated with diverse and flexible evolutionary paths that
group into four major trajectories. We conducted a meta-analysis of 18 lineages
containing species that use C, C, or intermediate C-C forms of
photosynthesis to parameterise a 16-dimensional phenotypic landscape. We then
developed and experimentally verified a novel Bayesian approach based on a
hidden Markov model that predicts how the C phenotype evolved. The
alternative evolutionary histories underlying the appearance of C
photosynthesis were determined by ancestral lineage and initial phenotypic
alterations unrelated to photosynthesis. We conclude that the order of C
trait acquisition is flexible and driven by non-photosynthetic drivers. This
flexibility will have facilitated the convergent evolution of this complex
trait
Cytosine-to-Uracil Deamination by SssI DNA Methyltransferase
The prokaryotic DNA(cytosine-5)methyltransferase M.SssI shares the specificity of eukaryotic DNA methyltransferases (CG) and is an important model and experimental tool in the study of eukaryotic DNA methylation. Previously, M.SssI was shown to be able to catalyze deamination of the target cytosine to uracil if the methyl donor S-adenosyl-methionine (SAM) was missing from the reaction. To test whether this side-activity of the enzyme can be used to distinguish between unmethylated and C5-methylated cytosines in CG dinucleotides, we re-investigated, using a sensitive genetic reversion assay, the cytosine deaminase activity of M.SssI. Confirming previous results we showed that M.SssI can deaminate cytosine to uracil in a slow reaction in the absence of SAM and that the rate of this reaction can be increased by the SAM analogue 5’-amino-5’-deoxyadenosine. We could not detect M.SssI-catalyzed deamination of C5-methylcytosine (m5C). We found conditions where the rate of M.SssI mediated C-to-U deamination was at least 100-fold higher than the rate of m5C-to-T conversion. Although this difference in reactivities suggests that the enzyme could be used to identify C5-methylated cytosines in the epigenetically important CG dinucleotides, the rate of M.SssI mediated cytosine deamination is too low to become an enzymatic alternative to the bisulfite reaction. Amino acid replacements in the presumed SAM binding pocket of M.SssI (F17S and G19D) resulted in greatly reduced methyltransferase activity. The G19D variant showed cytosine deaminase activity in E. coli, at physiological SAM concentrations. Interestingly, the C-to-U deaminase activity was also detectable in an E. coli ung+ host proficient in uracil excision repair
Interplay between pleiotropy and secondary selection determines rise and fall of mutators in stress response
Dramatic rise of mutators has been found to accompany adaptation of bacteria
in response to many kinds of stress. Two views on the evolutionary origin of
this phenomenon emerged: the pleiotropic hypothesis positing that it is a
byproduct of environmental stress or other specific stress response mechanisms
and the second order selection which states that mutators hitchhike to fixation
with unrelated beneficial alleles. Conventional population genetics models
could not fully resolve this controversy because they are based on certain
assumptions about fitness landscape. Here we address this problem using a
microscopic multiscale model, which couples physically realistic molecular
descriptions of proteins and their interactions with population genetics of
carrier organisms without assuming any a priori fitness landscape. We found
that both pleiotropy and second order selection play a crucial role at
different stages of adaptation: the supply of mutators is provided through
destabilization of error correction complexes or fluctuations of production
levels of prototypic mismatch repair proteins (pleiotropic effects), while rise
and fixation of mutators occur when there is a sufficient supply of beneficial
mutations in replication-controlling genes. This general mechanism assures a
robust and reliable adaptation of organisms to unforeseen challenges. This
study highlights physical principles underlying physical biological mechanisms
of stress response and adaptation
Tumor suppressor p53 binds with high affinity to CTG-CAG trinucleotide repeats and induces topological alterations in mismatched duplexes
DNA binding is central to the ability of p53 to function as a tumor suppressor. In line with the remarkable functional versatility of p53, which can act on DNA as a transcription, repair, recombination, replication, and chromatin accessibility factor, the modes of p53 interaction with DNA are also versatile. One feature common to all modes of p53-DNA interaction is the extraordinary sensitivity of p53 to the topology of its target DNA. Whereas the strong impact of DNA topology has been demonstrated for p53 binding to sequence-specific sites or to DNA lesions, the possibility that DNA structure-dependent recognition may underlie p53 interaction with other types of DNA has not been addressed until now. We demonstrate for the first time that conformationally flexible CTG·CAG trinucleotide repeats comprise a novel class of p53-binding sites targeted by p53 in a DNA structure-dependent mode in vitro and in vivo. Our major finding is that p53 binds to CTG·CAG tracts by different modes depending on the conformation of DNA. Although p53 binds preferentially to hairpins formed by either CTG or CAG strands, it can also bind to linear forms of CTG·CAG tracts such as canonic B DNA or mismatched duplex. Intriguingly, by binding to a mismatched duplex p53 can induce further topological alterations in DNA, indicating that p53 may act as a DNA topology-modulating factor
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