TABLE 4.
Gene type | First gene in operon | Relevant gene | No. of genes in operon | σ54 promoter sequencea | Reference |
---|---|---|---|---|---|
Genes known to be required for A motility | MXAN2991 | aglZ | 1 | TGGCAAC-N4-CTGCT | 34 |
MXAN3502 | agmI | 2 | TGGGGCG-N4-TTGCC | 35 | |
MXAN4799 | agmC | 2 | TGACAGA-N4-TTTCA | 35 | |
MXAN5818 | agmR | 2 | TGGCACA-N4-GTGCT | 35 | |
MXAN5820 | agmM | 1 | TGGCCCT-N4-CTGCT | 35 | |
Genes known to be required for sporulation | MXAN2269 | mspA | 1 | TGGCCTA-N4-GTGCT | 3 |
MXAN3225 | exo | 5 | TGGCACA-N4-CTGCT | 21 | |
MXAN5432 | tps | 2 | TGGGGCA-N4-TTGCT | 18 |
The putative promoter regions of operons containing A-motility and sporulation genes were analyzed using the M. xanthus genome sequence (5) and PromScan (http://molbiol-tools.ca/promscan/), a bioinformatics tool that was specifically developed to identify σ54-RNA polymerase binding sites in the sequences of bacterial DNA. To be designated a σ54 promoter, there had to be a potential binding site for σ54-RNA polymerase and a potential EBP binding site, which is a tandem repeat of at least 7 bp (27). On the basis of tests done with known promoter sequences and intragenic sequences, we estimated that our analysis had a false-positive rate of about 4% and a false-negative rate of about 23%. The −12 and −24 regions of the putative σ54 promoters are shown. Bold, underlined nucleotides are those that match nucleotides in the σ54 consensus sequence, which is TGGCACG-N4-TTGC(T/A) (1).