All entries for Monday 09 January 2006
January 09, 2006
Writing about web page http://dx.doi.org/10.1016/S0966-842X(00)01709-1
The Atkinson 2003 synthetic gene circuit relies among others on components of the bacterial nitrogen regulation system, more precisely on
- the glnG gene and its product, the NRI protein
- the glnAp2 promoter (product of glnA gene is GS) (requires NRI-P for activation)
- the glnKp promoter (also requires NRI-P for activation, activation less potent) (prodcut of glnK gene is glnK protein, PII like, see below)
To have a better understanding where these components are coming from I had a look at the above named paper Ninfa 2000 .
It seem noteworthy that NRI-P has a inhibiting influence on the glnA transcritption at higher concentrations, and that glnK is only expressed at these higher concentrations. Or so I understand the description of the various levels of the response to nitrogen stress, see below .
- PII proteins, found in bacteria, Archaea and plants, are involved in coordinating carbon and nitrogen assimilation by regulation of correponding signal transduction enzymes. They integrate antagonistic signals of carbon and nitrogen status.
- developmental regulation systems probably eveolved from metabolic regulation systems.
- switching between regulatory cell types depending on carbon-nitrogen condition is reversible, but cell should not flip back and forth to often -> certain constraints.
- PII is direct and indirect sensor of various stimuli that cause the formation of different PII conformations
Nitrogen regulation in E. coli
- if ammonia is present, assimilation of ammonia into glutamine is regulated in response to the intracellular concentration of glutamine (nitrogen signal) and 2-ketoglutarate (2KG) (carbon signal).
- glutamine synthetase (GS) is responsible for most of the ammonia assimilation, closely regulated and limits the rate of nitrogen assimilation to keep it in balance with the rate of caron assimilation.
- GS regulated by a) regulation of its structural gene glnA and b) by regulation of GS activity by reversible covalent adenylylation.
- Adenylylation state of GS is controlled by the bifunctional enzyme adenylyltransferase (ATase)
- transcription of glnA requires transcription factor NRI-P (phosporylated NRI)
- phosphorylation of NRI is controlled by NRII
- So NRII and ATase control level and activity (respectively) and are at least in part controlled by PII
Role of PII
- PII inhibits autophosphorylation of NRII and activates its phophatase activity -> results in decrease in the extent of NRI phosphorylation.
- PII, by binding to ATase, activates GS adenylylation.
Regulation of PII
- PII activity in turn is regulated by small-molecule signals of carbon and nitrogen status:
PII regulation by nitrogen signal
- Glutamine is sensed by ATase and a bifunctional uridylyltransferase-uridylylremoving enzyme UTase-UR, which controls PII activity: it uridylylates PII if glutamine concentration is low and deuridylylates PII when the glutamine concentration is high.
- PII-UMP does not bind to NRII, thus at low glutamine, NRII can phosphorylate NRI, thus turning on nitrogen-regulated gene expresion Ntr including glnA, gene of GS.
- Further PII-UMP binds to ATase, stimulating deadenylylation of GS-AMP, activating GS.
PII regulation by carbon signal
- Carbon signals, mainly 2KG, directly bind to PII, which as a trimer has three binding sites for 2KG and ATP. Synergistic dynamics lead to binding of one 2KG and three ATP at normal concentrations and saturation of PII only at very high 2KG levels.
- 2KG saturated PII cannot interact with NRII or ATase. So carbon signal can counteract the effect of the nitrogen signal.
- Signals are sensed independently since saturation of PII by 2KG does not affect its interaction with UTase-UR.
- Concentration of the components of the signal transduction system must be balanced
- Level One: Increase of NRI and NRII expression.
- Level Two: Switching on of Ntr genes.
- Level Three: Switching on of nif genes (in some organisms).
Closer look at switch from first two second level response:
- The transcription factor NRI-P binds upstream enhancers and interacts with sigma RNA polymerase at the target promoters by means of a DNA loop, whose stability is further regulated by other factors.
- Boils down to: Each Ntr promoter becomes activated only when the NRI-P concentration is above a certain threshhold.
- Negative regulation of NRI-P has also been observed. In particular, the expression of glnA first increases and then decreases at high NRI-P concentrations.
- The Ntr genes of the second level require a higher level of NRI-P concentration than the glnA promoter.
- One second level gene is GlnK, which encodes the PII like protein GlnK, which seems to be designed to function under nitrogen starvation conditions. It might serve a role similar to PII or replacing it under these conditions. Not fully understood.