scholarly journals 18 TILRR Functional Mutants Selectively Inhibit Inflammatory and Anti-Apoptotic Responses

Heart ◽  
2012 ◽  
Vol 98 (Suppl 3) ◽  
pp. A6.1-A6
Author(s):  
M Neilan ◽  
X Zhang ◽  
T Steiner ◽  
J Boyle ◽  
S Francis ◽  
...  
Keyword(s):  
Genetics ◽  
1980 ◽  
Vol 94 (4) ◽  
pp. 859-870
Author(s):  
Takehiro Oshima ◽  
Isamu Takano

ABSTRACT Mutation of the two homothallic genes, HMLα/HMLa and HMRa/HMRα, in homothallic strains of Saccharomyces cereuisiae was studied. Of 11 mutants of the HMLa gene, eight were due to a phenotypic mutation from HMLα to HMLa, i.e., a mutation causing a change in function of the original HML allele to that of the other HML allele (functional mutation), and three were due to a defective mutation at the HMLα gene, i.e., a mutation causing a non-functional allele (nonfunctional mutation). All 14 mutants of the HMRa gene, on the other hand, were due to a phenotypic mutation from HMRa to HMRα i.e., a functional mutation. Phenotypic reverse mutations, i.e., HMLa to HMLα and HMRα to HMRa, were also observed in the cultivation of EMS (ethyl methanesulfonate) treated spores having the HO HMRα HMLa genotype. Mutation from heterothallic cells to homothallism was observed in a nonfunctional mutant of the HMLα gene, by mutagenesis with EMS, but not in the functional mutants of the HMLα and HMRa genes or in the authentic strains having the α HO HMRα HMLα (α Hp) and a HO HMRa HMLa (a Hq) genotypes. These observations suggest that the functional mutation is not caused by the direct mutation from a homothallic allele to the opposite, but by replacement of a transposable genic element produced from a homothallic locus with a region of a different homothallic locus. These observations also support the controlling-element model and the cassette model, which have been proposed to explain the mating-type differentiation by the homothallic genes.


2005 ◽  
Vol 49 (8) ◽  
pp. 3421-3427 ◽  
Author(s):  
Fahd K. Majiduddin ◽  
Timothy Palzkill

ABSTRACT Carbapenem antibiotics are used as antibiotics of last resort because they possess a broad spectrum of antimicrobial activity and are not easily hydrolyzed by β-lactamases. Recently, class A enzymes, such as the SME-1, NMC-A, and IMI-1 β-lactamases, have been identified with the capacity to hydrolyze carbapenem antibiotics. Traditional class A β-lactamases, such as TEM-1 and SHV-1, are unable to hydrolyze carbapenem antibiotics and exhibit some differences in sequence from those that are able to hydrolyze carbapenem antibiotics. The positions that differ may contribute to the unique substrate specificity of the class A carbapenemase SME-1. Codons in the SME-1 gene representing residues 104, 105, 132, 167, 237, and 241 were randomized by site-directed mutagenesis, and functional mutants were selected for the ability to hydrolyze imipenem, ampicillin, or cefotaxime. Although several positions are important for hydrolysis of β-lactam antibiotics, no single position was found to uniquely contribute to carbapenem hydrolysis. The results of this study support a model whereby the carbapenemase activity of SME-1 is due to a highly distributed set of interactions that subtly alter the structure of the active-site pocket.


1985 ◽  
Vol 4 (2) ◽  
pp. 509-513 ◽  
Author(s):  
J. Vacher ◽  
M. Springer ◽  
R.H. Buckingham

1973 ◽  
Vol 241 (105) ◽  
pp. 13-14 ◽  
Author(s):  
P. M. NAHA

1997 ◽  
Vol 93 (4) ◽  
pp. 335-341 ◽  
Author(s):  
Qiuping Zhang ◽  
Elisabeth Cavallero ◽  
Michael M. Hoffmann ◽  
Julian Cavanna ◽  
Andrea Kay ◽  
...  

1. The common association of obesity, diabetes mellitus and hyperlipidaemia may have a primary aetiological basis. Insulin resistance has been postulated as a possible cause, but defects in the plasma transport of triacylglycerol or fatty acids could also be primary determinants. 2. We have therefore, studied 18 patients with diabetes mellitus, obesity and severe hypertriglyceridaemia for defects of a key protein involved in the clearance of plasma triacylglycerols, lipoprotein lipase. 3. DNA was prepared from leucocytes of 18 patients with the above syndrome, and exons encoding lipoprotein lipase were amplified by PCR. The products were sequenced using the dideoxy chain-termination method. 4. Eight of the subjects were found to possess genetic variants at the lipoprotein lipase gene locus. These were: (a) G579→A, V108V; (b) G818→A, G188E; (c) C829→T, R192; (d) A1127→G, N291S; (e) C1308→G, F351L;(f) C1338→A, T361T; and (g) C1595→G, S447. Three of these, (c), (e) and (f), have not hitherto been described. Variant (f), appears to be a population polymorphism whose allele frequency in normolipidaemic diabetics was found to be 0.12 (162 chromosomes studied). The others are all rare at frequencies of <0.01 and may contribute to the phenotype by impairing clearance of plasma triacylglycerols. 5. We conclude that genetic variants at the lipoprotein lipase locus occur commonly in subjects with this syndrome (four out of 18 subjects with probably functional mutants) and may affect the individual's response to obesity and diabetes mellitus for the development of lipaemia.


Cancers ◽  
2021 ◽  
Vol 13 (17) ◽  
pp. 4413
Author(s):  
Sol-Bi Shin ◽  
Dae-Hoon Kim ◽  
Da-Eun Kim ◽  
Mark Borris D. Aldonza ◽  
Yoosik Kim ◽  
...  

To overcome the limitations of chemoresistance, combination therapies using druggable targets have been investigated. Our previous studies led us to hypothesize that the downregulation of PLK1 expression or activity can be one strategy to overcome the hurdles of taxane resistance by the downregulation of ABC transporters. To explore this, various versions of PLK1 including a constitutively active version, kinase-dead form, and polo-box domain mutant were expressed in paclitaxel-resistant lung adenocarcinoma (LUADTXR). Targeting PLK1 using shRNA or non-functional mutants downregulated ABCB1, ABCC9, and ABCG2 in LUADTXR cells, which was similar to the downregulation effects from treatment with PLK1 inhibitors. The high expression of EGFR in LUAD led us to administer gefitinib, showing a markedly reduced EGFR level in LUADTXR cells. When gefitinib and PLK1 inhibitors were combined, LUADTXR cells tended to undergo apoptosis more effectively than parental cells, showing a synergistic effect on the downregulation of ABC transporters through c-Myc and AP-1. Clinical data provide evidence for the relevance between survival rates and expressions of PLK1 and EGFR in LUAD patients. Based on these results, we suggest that a combination of gefitinib and PLK1 inhibitors exerts strong synergism in LUADTXR, which helps to overcome the limitations associated with taxanes.


2021 ◽  
Author(s):  
◽  
Alexandra Bauer Housh

Tracers are used for qualitative and quantitative investigation of a system. Radiotracers have a radionuclide to observe chemical or biological processes by detection of the radionuclide's decay energy. They are non-disruptive and non-destructive to living systems and can be quantified, imaged, and measured in real time, adding value. This work focuses on radiochemistry and radiotracer techniques to understand maize uptake and localization of micronutrients and the impact of Azospirillum brasilense microbial interactions on these processes. Further, it explored how such interactions can influence stress responses in maize. Finally, it examined how the natural biological functions of A. brasilense bacteria respond to light stimulus conducted through the plant tissues. In this dissertation, the efficacy of using 4-fluorophenylboronic acid (FPBA) as a boton (B) imaging agent, which is a derivative of the B deficiency mimic phenylboronic acid (PBA), was explored. It is shown that radioactively labelled [18F]FPBA (t [subscript 1/2] [equals] 110 m) accumulates at the root tip, the root elongation zone and at lateral root initiation sites in maize roots, and also translocates to the shoot where it accumulates along leaf edges. This is the first time a radiotracer has been utilized to image B in plant systems. Nutritional iron (Fe) content was explored in Azospirillum brasilense associated maize. 59Fe (t [subscript 1/2] [equals] 44.5 d) was used to trace iron uptake kinetics and allocation to leaf. In the presence of functional mutants of this bacteria, iron uptake and allocation to leaf was enhanced in maize seedlings. Maize were grown to maturity and plants associated with the bacteria had greater crop yield (kernels cob-1) and enhanced iron and protein ferritin- the bioavailable form of iron to humans- seed content. Similar studies were completed using zinc (65Zn, t¬Ω= 244 d), where it was noted that the presence of the low-auxin producing and nitrogen-fixing bacteria strain, ipdC, enhanced zinc uptake but had no enhancement effect on allocation or zinc seed filling. Carbon metabolism in response to stresses and microbial interaction was also investigated in maize with [11C]CO2 (t [subscript 1/2] [equals] 20.4 m) radiotracer. In association with A. brasilense, maize fixed more carbon dioxide, allocated more 11C-photosynthates to the roots, and produced more 11C-exudates than control maize. Metabolic differences were studied via radio-HPLC and radio-TLC to reveal association enhanced 11C flow into hydrophobic structural components and amino acids. When nitrogen stressed, non-inoculated maize exhibited a decrease in carbon dioxide fixation, root allocation of 11C-photosynthates, and decreased 11Cexudation compared to control maize. They also saw increased 11C flow into hydrophobic structural components and sugars. When inoculated with A. brasilense and subjected to nitrogen stress, the same enhancements occurred- but fixation, allocation, and exudation recovered to near control maize levels, suggesting these bacteria ameliorate some abiotic stresses. Finally, 59Fe and [11C]CO2 radiotracers were applied to the functional mutants of A. brasilense to uncover how various biological functions were impacted by light exposure. First, light transmittance from shoot to root tissues, called light piping, in maize was shown using a DSLR camera and image intensifier. Studies showed the functional mutants with biological nitrogen fixation (BNF) capacity had enhanced assimilation of 59Fe when exposed to light relative to dark treatments and greater activity of the nitrogenase enzyme as measured by acetylene reduction assay in light, with a greater response noted for red than blue light wavelengths. Carbon assimilation as [11C]CO2 and subsequent metabolism in these bacteria were also impacted by light stimulus.


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