GcvB RNA | |
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![]() Predicted secondary structure and sequence conservation of GcvB | |
Identifiers | |
Symbol | GcvB |
Rfam | RF00022 |
Other data | |
RNA type | Gene |
Domain(s) | Bacteria |
SO | SO:0000379 |
PDB structures | PDBe |
The gcvB RNA gene encodes a small non-coding RNA involved in the regulation of a number of amino acid transport systems as well as amino acid biosynthetic genes. The GcvB gene is found in enteric bacteria such as Escherichia coli . GcvB regulates genes by acting as an antisense binding partner of the mRNAs for each regulated gene. This binding is dependent on binding to a protein called Hfq. Transcription of the GcvB RNA is activated by the adjacent GcvA gene and repressed by the GcvR gene. [1] A deletion of GcvB RNA from Y. pestis changed colony shape as well as reducing growth. [2] It has been shown by gene deletion that GcvB is a regulator of acid resistance in E. coli. GcvB enhances the ability of the bacterium to survive low pH by upregulating the levels of the alternate sigma factor RpoS. [3] A polymeric form of GcvB has recently been identified.[ citation needed ] Interaction of GcvB with small RNA SroC triggers the degradation of GcvB by RNase E, lifting the GcvB-mediated mRNA repression of its target genes. [4]
GcvB has been shown to regulate a large number of genes in E. coli and Salmonella species. GcvB was shown to bind to Oppa and DppA which transport oligopeptides and dipeptides respectively. [5] [6] It has been shown to also regulate gltL, argT, STM, livK, livJ, brnQ, sstT and cycA which are involved in uptake of a variety of amino acids. [7] [8] [9] GcvB RNA also is involved in regulating a variety of genes involved in amino acid biosynthesis such as ilvC, gdhA, thrL and serA. [10] GcvB RNA binds PhoPQ mRNA, which encodes a two-component system involved in magnesium homeostasis. [11]
There is evidence that E. coli GcvB can form polymers. Native polyacrylamide gel electrophoresis was used to show a higher molecular weight band corresponding to a potential polymer. [12] Transmission electron microscopy was then used to identify a filamentous structure for the polymer. However, the authors suggest that these long filaments are unlikely to be physiologically relevant. It was shown that a construct containing only the first 61 nucleotides including the first stem-loop was sufficient for polymerisation. Similar results were recently shown for the DsrA RNA. [13] The physiological relevance of polymerisation is not known.
The GcvB RNA is found in a range of bacteria including: [14]