| Autor: |
Katona LI; Department of Molecular Genetics and Microbiology, Center for Infectious Diseases, Stony Brook University, Stony Brook, NY, USA. |
| Jazyk: |
angličtina |
| Zdroj: |
Microbiology (Reading, England) [Microbiology (Reading)] 2015 Nov; Vol. 161 (11), pp. 2243-55. Date of Electronic Publication: 2015 Aug 27. |
| DOI: |
10.1099/mic.0.000166 |
| Abstrakt: |
Borrelia burgdorferi is the causative agent of Lyme disease. In B. burgdorferi, RpoS controls the expression of virulence genes needed for mammalian infection. The Fur homologue BosR regulates the transcription of rpoS and therefore BosR determines, albeit indirectly, the infection status of the spirochaete. Transcription of rpoS in B. burgdorferi is complex: rpoS can be transcribed either from an RpoD-dependent promoter to yield a long transcript or from an RpoN-dependent promoter to yield a short transcript. This study shows that BosR repressed synthesis of the long transcript while at the same time activating synthesis of the short transcript. How BosR does this is unclear. To address this, spirochaetes were engineered to express either BosR or the naturally occurring variant BosRR39K. Mice became infected by the spirochaetes expressing BosR but not by the spirochaetes expressing BosRR39K. Furthermore, the spirochaetes expressing BosR activated rpoS transcription during growth in culture whereas the spirochaetes expressing BosRR39K did not. Thus, BosR's activation of rpoS transcription somehow involves Arg39. This arginine is highly conserved in other FUR proteins and therefore other FUR proteins may also require this arginine to function. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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