scholarly journals Chemical and functional characterization of an altered form of ribosomal protein S4 derived from a strain ofE. colidefective in auto-regulation of the alpha operon

1986 ◽  
Vol 14 (17) ◽  
pp. 6929-6944 ◽  
Author(s):  
Li-Ming Changchien ◽  
Richard C. Conrad ◽  
Gary R. Craven
1983 ◽  
Vol 3 (5) ◽  
pp. 761-772
Author(s):  
S Chang ◽  
J J Wasmuth

Starting with hybrid cell lines between a Chinese hamster cell EmtA mutant and a Chinese hamster cell EmtB mutant, we have constructed cell lines that are homozygous for mutant alleles at both the emtA locus and the emtB locus, by using a two-step segregation protocol. The EmtA EmtB double mutants are approximately 10-fold more resistant to emetine inhibition than either of the parental mutants. Having both the EmtA mutation and the EmtB mutation expressed in the same cell also results in a level of resistance to cryptopleurine that is significantly higher than a simple additive effect of the two mutations alone. Analysis of ribosomal proteins by two-dimensional polyacrylamide gel electrophoresis demonstrated that a parental hybrid and a first-step segregant, which has lost the wild-type emtA allele, synthesize both a normal and an altered form of ribosomal protein S14, whereas an EmtA EmtB double mutant synthesizes only the altered form of this ribosomal protein. This result confirms that the emtB locus is the structural gene for ribosomal protein S14. Our results also suggest that the products of the emtA and emtB loci interact directly, indicating that the emtA locus, like the emtB locus, encodes a component of the ribosome.


PLoS ONE ◽  
2012 ◽  
Vol 7 (8) ◽  
pp. e42523 ◽  
Author(s):  
Drago Perina ◽  
Marina Korolija ◽  
Andreja Mikoč ◽  
Maša Roller ◽  
Bruna Pleše ◽  
...  

2009 ◽  
Vol 55 (2) ◽  
pp. 111-125 ◽  
Author(s):  
Ivailo Simoff ◽  
Hossein Moradi ◽  
Odd Nygård

2007 ◽  
Vol 102 (4) ◽  
pp. 473-479 ◽  
Author(s):  
Mariana Pérez-Escobar ◽  
Ana María Cevallos ◽  
Bertha Espinoza ◽  
Norma Espinosa ◽  
Ignacio Martínez ◽  
...  

Author(s):  
Xiaobang Hu ◽  
Weijie Wang ◽  
Donghui Zhang ◽  
Jianhua Jiao ◽  
Wenbin Tan ◽  
...  

1983 ◽  
Vol 3 (5) ◽  
pp. 761-772 ◽  
Author(s):  
S Chang ◽  
J J Wasmuth

Starting with hybrid cell lines between a Chinese hamster cell EmtA mutant and a Chinese hamster cell EmtB mutant, we have constructed cell lines that are homozygous for mutant alleles at both the emtA locus and the emtB locus, by using a two-step segregation protocol. The EmtA EmtB double mutants are approximately 10-fold more resistant to emetine inhibition than either of the parental mutants. Having both the EmtA mutation and the EmtB mutation expressed in the same cell also results in a level of resistance to cryptopleurine that is significantly higher than a simple additive effect of the two mutations alone. Analysis of ribosomal proteins by two-dimensional polyacrylamide gel electrophoresis demonstrated that a parental hybrid and a first-step segregant, which has lost the wild-type emtA allele, synthesize both a normal and an altered form of ribosomal protein S14, whereas an EmtA EmtB double mutant synthesizes only the altered form of this ribosomal protein. This result confirms that the emtB locus is the structural gene for ribosomal protein S14. Our results also suggest that the products of the emtA and emtB loci interact directly, indicating that the emtA locus, like the emtB locus, encodes a component of the ribosome.


2020 ◽  
Vol 477 (7) ◽  
pp. 1261-1286 ◽  
Author(s):  
Marie Anne Richard ◽  
Hannah Pallubinsky ◽  
Denis P. Blondin

Brown adipose tissue (BAT) has long been described according to its histological features as a multilocular, lipid-containing tissue, light brown in color, that is also responsive to the cold and found especially in hibernating mammals and human infants. Its presence in both hibernators and human infants, combined with its function as a heat-generating organ, raised many questions about its role in humans. Early characterizations of the tissue in humans focused on its progressive atrophy with age and its apparent importance for cold-exposed workers. However, the use of positron emission tomography (PET) with the glucose tracer [18F]fluorodeoxyglucose ([18F]FDG) made it possible to begin characterizing the possible function of BAT in adult humans, and whether it could play a role in the prevention or treatment of obesity and type 2 diabetes (T2D). This review focuses on the in vivo functional characterization of human BAT, the methodological approaches applied to examine these features and addresses critical gaps that remain in moving the field forward. Specifically, we describe the anatomical and biomolecular features of human BAT, the modalities and applications of non-invasive tools such as PET and magnetic resonance imaging coupled with spectroscopy (MRI/MRS) to study BAT morphology and function in vivo, and finally describe the functional characteristics of human BAT that have only been possible through the development and application of such tools.


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