| Autor: |
Heindl JE; 1Department of Biology, Indiana University, Bloomington, IN 47405, USA.; 2Department of Biological Sciences, University of the Sciences in Philadelphia, Philadelphia, PA 19104, USA., Crosby D; 2Department of Biological Sciences, University of the Sciences in Philadelphia, Philadelphia, PA 19104, USA.; †Present address: Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, PA 15213, USA., Brar S; 2Department of Biological Sciences, University of the Sciences in Philadelphia, Philadelphia, PA 19104, USA., Pinto JF; 2Department of Biological Sciences, University of the Sciences in Philadelphia, Philadelphia, PA 19104, USA., Singletary T; 2Department of Biological Sciences, University of the Sciences in Philadelphia, Philadelphia, PA 19104, USA., Merenich D; 2Department of Biological Sciences, University of the Sciences in Philadelphia, Philadelphia, PA 19104, USA., Eagan JL; 1Department of Biology, Indiana University, Bloomington, IN 47405, USA., Buechlein AM; 3Center for Genomics and Bioinformatics, Indiana University, Bloomington, IN 47405, USA., Bruger EL; 4Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA.; ‡Present address: Department of Biological Sciences, University of Idaho, Moscow, ID 83844, USA., Waters CM; 4Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA., Fuqua C; 1Department of Biology, Indiana University, Bloomington, IN 47405, USA. |
| Abstrakt: |
A core regulatory pathway that directs developmental transitions and cellular asymmetries in Agrobacterium tumefaciens involves two overlapping, integrated phosphorelays. One of these phosphorelays putatively includes four histidine sensor kinase homologues, DivJ, PleC, PdhS1 and PdhS2, and two response regulators, DivK and PleD. In several different alphaproteobacteria, this pathway influences a conserved downstream phosphorelay that ultimately controls the phosphorylation state of the CtrA master response regulator. The PdhS2 sensor kinase reciprocally regulates biofilm formation and swimming motility. In the current study, the mechanisms by which the A. tumefaciens sensor kinase PdhS2 directs this regulation are delineated. PdhS2 lacking a key residue implicated in phosphatase activity is markedly deficient in proper control of attachment and motility phenotypes, whereas a kinase-deficient PdhS2 mutant is only modestly affected. A genetic interaction between DivK and PdhS2 is revealed, unmasking one of several connections between PdhS2-dependent phenotypes and transcriptional control by CtrA. Epistasis experiments suggest that PdhS2 may function independently of the CckA sensor kinase, the cognate sensor kinase for CtrA, which is inhibited by DivK. Global expression analysis of the pdhS2 mutant reveals a restricted regulon, most likely functioning through CtrA to separately control motility and regulate the levels of the intracellular signal cyclic diguanylate monophosphate (cdGMP), thereby affecting the production of adhesive polysaccharides and attachment. We hypothesize that in A. tumefaciens the CtrA regulatory circuit has expanded to include additional inputs through the addition of PdhS-type sensor kinases, likely fine-tuning the response of this organism to the soil microenvironment. |
