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Dr. Luis Rogelio Cruz-Vera
Assistant Professor
Department of Biological Sciences


 

 

 

 

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Molecular Biology, Microbiology
Translation and Gene expression regulation


Research Description

 

Our goal is to understand how biomolecules can modulate the ribosome function to influence gene expression, metabolism and cellular phenotype.

Translation elongation can be controlled by diverse mechanisms since a substantial number of different factors and events are involved in the process. Despite the diversity, the elongation regulatory mechanisms keep two common and essential characteristics: 1) the translated sequence itself plays an important role in the regulatory process; and 2) the inhibition, or delay in the elongation due to a regulated event can lead to the accumulation of the involved translating peptidyl-tRNA. The objective of our research is to identify genes subject to translation elongation regulation in several model organisms detecting peptidyl-tRNAs involved in the gene expression under relevant cell growth conditions. Also, determine the molecular mechanism(s) responsible for these translational regulation examples. We expect to produce a gene-expression profiling technology to analyze in vivo other important phenomena related to the accumulation of peptidyl-tRNA such as: the action of antibiotic translation inhibitors, codon translation efficiency, coupling translation-protein folding, among other processes.

Selected Publications

  • Cruz-Vera, L. R., Gong, M. and Yanofsky, C. (2008). Physiological effects of anti-TRAP protein activity and tRNA(Trp) charging on trp operon expression in Bacillus subtilis. J. Bacteriol. 190:1937-1945
  • Gong, M., Cruz-Vera, L. R. and Yanofsky, C. (2007). Ribosome recycling factor and release factor 3 action promotes TnaC-peptidyl-tRNA drop off and relieves ribosome stalling during tryptophan induction of tna oepron expression in Escherichia coli. J. Bacteriol. 189:3147-3155
  • Cruz-Vera, L. R., Rajagopal, S., Squires, C. and Yanofsky, C. (2005). Features of ribosome-peptidyl-tRNA interactions essential for tryptophan induction of tna operon expression. Mol. Cell. 19:333-343
  • Cruz-Vera, L. R., Magos-Castro, M. A., Zamora-Romo, E. and Guarneros, G. (2004). Ribosome stalling and peptidyl-tRNA drop-off during translation delay at AGA codons. Nucleic Acids Res. 18:4462-4468

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Copyright © 2006 Biological Sciences, UAH. All rights reserved.