The Brazilian GMO Regulatory System: A Historical View and Perspective

Author(s):  
Edivaldo Domingues Velini ◽  
Maria Lúcia Zaidan Dagli ◽  
Gutemberg Delfino de Souza ◽  
Rubens José Nascimento ◽  
Tassiana Fronza Pinho ◽  
...  
1987 ◽  
Vol 7 (7) ◽  
pp. 2367-2377 ◽  
Author(s):  
N Segev ◽  
D Botstein

The Saccharomyces cerevisiae gene YPT1 encodes a protein that exhibits significant homology to the mammalian ras proteins. Using gene disruption techniques, we have shown that the intact YPT1 gene is required for spore viability. Lethality caused by loss of YPT1 function, unlike that caused by loss of the yeast ras homologs RAS1 and RAS2 function, is not suppressed by the bcy1 mutation, suggesting that YPT1 does not act through the adenylate cyclase regulatory system. A cold-sensitive allele, ypt1-1, was constructed. At the nonpermissive temperature, mutants died, exhibiting aberrant nuclear morphology, as well as abnormal distribution of actin and tubulin. The mutant cells died without exhibiting classical cell-cycle-specific arrest; nevertheless, examination of cellular DNA content suggests that the YPT1 function is required, particularly after S phase. Cells carrying the ypt1-1 mutation died upon nitrogen starvation even at a temperature permissive for growth; diploid cells homozygous for ypt1-1 did not sporulate. The YPT1 gene is thus involved in nutritional regulation of the cell cycle as well as in normal progression through the mitotic cell cycle.


Author(s):  
Tony Carden ◽  
Natassia Goode ◽  
Paul Salmon

Led outdoor activities such as rock climbing, canoeing, and hiking, involve intentional engagement with risk. Organizations that provide these activities are obliged to manage risk by eliminating or minimizing health and safety risks so far as is reasonably practicable. Regulating safety across this industry sector therefore presents special challenges. The current regulatory environment for led outdoor activity safety in Victoria, Australia consists of multiple, loosely connected instruments and agencies. This study used Work Domain Analysis to develop a model of the functional structure of the regulatory system. The model was then used in interviews with domain experts to identify problems with the structure, efficiency and effectiveness of the regulatory system. A model of the functional structure of the system was developed and system weaknesses identified. Next steps toward reform of this system and implications for other regulatory regimes are discussed.


1998 ◽  
Vol 180 (1) ◽  
pp. 20-26 ◽  
Author(s):  
Hai-Ping Cheng ◽  
Graham C. Walker

ABSTRACT The Rhizobium meliloti exoS gene is involved in regulating the production of succinoglycan, which plays a crucial role in the establishment of the symbiosis between R. melilotiRm1021 and its host plant, alfalfa. TheexoS96::Tn5 mutation causes the upregulation of the succinoglycan biosynthetic genes, thereby resulting in the overproduction of succinoglycan. Through cloning and sequencing, we found that the exoS gene is a close homolog of theAgrobacterium tumefaciens chvG gene, which has been proposed to encode the sensor protein of the ChvG-ChvI two-component regulatory system, a member of the EnvZ-OmpR family. Further analyses revealed the existence of a newly discovered A. tumefaciens chvI homolog located just upstream of the R. meliloti exoS gene. R. meliloti ChvI may serve as the response regulator of ExoS in a two-component regulatory system. By using ExoS-specific antibodies, it was found that the ExoS protein cofractionated with membrane proteins, suggesting that it is located in the cytoplasmic membrane. By using the same antibodies, it was shown that the exoS96::Tn5 allele encodes an N-terminal truncated derivative of ExoS. The cytoplasmic histidine kinase domain of ExoS was expressed in Escherichia coli and purified, as was the R. meliloti ChvI protein. The ChvI protein autophosphorylated in the presence of acetylphosphate, and the ExoS cytoplasmic domain fragment autophosphorylated at a histidine residue in the presence of ATP. The ChvI protein was phosphorylated in the presence of ATP only when the histidine kinase domain of ExoS was also present. We propose a model for regulation of succinoglycan production by R. meliloti through the ExoS-ChvI two-component regulatory system.


2005 ◽  
Vol 187 (14) ◽  
pp. 4967-4975 ◽  
Author(s):  
J. Newcombe ◽  
J. C. Jeynes ◽  
E. Mendoza ◽  
J. Hinds ◽  
G. L. Marsden ◽  
...  

ABSTRACT We previously identified and characterized a two-component regulatory system in the meningococcus with homology to the phoP-phoQ system in salmonella and showed that allele replacement of the NMB0595 regulator gene led to loss of virulence, sensitivity to antimicrobial peptides, perturbed protein expression, and magnesium-sensitive growth. On the basis of these findings we proposed that the system should be designated the meningococcal PhoPQ system. Here we further characterized the NMB0595 mutant and demonstrated that it had increased membrane permeability and was unable to form colonies on solid media with low magnesium concentrations, features that are consistent with disruption of PhoPQ-mediated modifications to the lipooligosaccharide structure. We examined the transcriptional profiles of wild-type and NMB0595 mutant strains and found that magnesium-regulated changes in gene expression are completely abrogated in the mutant, indicating that, similar to the salmonella PhoPQ system, the meningococcal PhoPQ system is regulated by magnesium. Transcriptional profiling of the mutant indicated that, also similar to the salmonella PhoPQ system, the meningococcal system is involved in control of virulence and remodeling of the bacterial cell surface in response to the host environment. The results are consistent with the hypothesis that the PhoP homologue plays a role in the meningococcus similar to the role played by PhoP in salmonella. Elucidating the role that the PhoPQ system and PhoPQ-regulated genes play in the response of the meningococcus to the host environment may provide new insights into the pathogenic process.


2020 ◽  
Vol 63 (3) ◽  
pp. 443-446
Author(s):  
Jian Xiao ◽  
Zhuofeng Lin ◽  
Hua Qin ◽  
Zhilong Zheng ◽  
Fanghua Gong ◽  
...  

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