![]() ![]() ![]() |
Name: | rmf | ||||||||||
Gene(s): | rmf Genome Browser M3D Gene expression COLOMBOS | ||||||||||
Note(s): | Analysis of gene expression has proved that under NlpE lipoprotein overexpression, the presence of the protein CpxR causes increased transcription of the rmf gene; however, no DNA sequence related to the consensus DNA-binding site of CpxR has been identified in the regulatory region of the gene. Therefore, the effect of CpxR on rmf is probably indirect Raivio TL,2013 An rmf mutant had reduced viability during stationary phase and did not contain ribosome dimers Yamagishi M,1993, whereas the essential role of RMF is for the storage of unused ribosomes under starvation conditions Shimada T,2013. Based on analysis using a promoter-specific transcription factor screening system (PS-TF), it has been shown that the rsd and rmf promoters are repressed by ArcA and activated by McbR, RcdA, SdiA, and SlyA transcription factors (TFs) during the transition from exponential to stationary growth phase. On the other hand, a total of 2 TFs (DsdC and PaaX) were estimated to bind to the rmf promoter Yoshida H,2018 The binding regions for TFs regulating rmf expression were predicted on the basis of the gel pattern. The order of the size increase of TF-binding sequences is as follows: ArcA < SlyA < McbR < RcdA < SdiA. The sizes of these TFs were basically the same as those observed with the rsd promoter Yoshida H,2018 The TFs are controlled by specific effector ligands which decrease in the presence of the corresponding effector, such as AcP for ArcA and AI-1 for SdiA, and increase in its presence, such as AI-2 for McbR, acetate for RcdA, and ppGpp for SlyA Yoshida H,2018 |
||||||||||
Evidence: | [COMP-AINF] Inferred computationally without human oversight [EXP-IDA-BOUNDARIES-DEFINED] Boundaries of transcription experimentally identified |
||||||||||
Reference(s): | [1] Aiso T., et al., 2005 | ||||||||||
Promoter | |||||||||||
Name: | rmfp | ||||||||||
+1: | 1015657 | ||||||||||
Distance from start of the gene: | 58 | ||||||||||
Sequence: |
tggcgtgaattttgcgcattgacggcagttatgattcgcggtattgcttaactgtgattgCacatttagtaatcactgttt |
||||||||||
Evidence: | [EXP-IDA-TRANSCRIPTION-INIT-MAPPING] | ||||||||||
Reference(s): | [1] Aiso T., et al., 2005 | ||||||||||
Terminator(s) | |||||||||||
Type: | rho-independent | ||||||||||
Sequence: | tctttaaaaaGAAACCTCCGCATTGCGGAGGTTTCgccttttgat | ||||||||||
Reference(s): | [1] Aiso T., et al., 2005 |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
nd | ArcA-phosphorylated | repressor | rmfp | nd | nd | nd | nd | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [EXP-GSELEX], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [3] |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
remote | CRP-cyclic-AMP | activator | rmfp | 1015536 | 1015552 | -113.5 | tgcggaaaaaTTTGTTCCTCTTCACATtttttgtaca | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [COMP-AINF-SIMILAR-TO-CONSENSUS], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [2] |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
nd | McbR | activator | rmfp | nd | nd | nd | nd | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [EXP-GSELEX], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [3] |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
nd | RcdA | activator | rmfp | nd | nd | nd | nd | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [EXP-GSELEX], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [3] |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
nd | SdiA | activator | rmfp | nd | nd | nd | nd | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [EXP-GSELEX], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [3] |
Type | Transcription factor | Function | Promoter | Binding Sites | Growth Conditions | Evidence | Confidence level (C: Confirmed, S: Strong, W: Weak) | Reference(s) | |||
---|---|---|---|---|---|---|---|---|---|---|---|
LeftPos | RightPos | Central Rel-Pos | Sequence | ||||||||
nd | SlyA | activator | rmfp | nd | nd | nd | nd | nd | [EXP-IEP-GENE-EXPRESSION-ANALYSIS], [EXP-GSELEX], [EXP-IDA-BINDING-OF-PURIFIED-PROTEINS] | W | [3] |
Evidence: | [EXP-IEP] Inferred from expression pattern |
Reference(s): | [4] Izutsu K., et al., 2001 |
RNA cis-regulatory element | ![]() |
---|
Regulation, transcriptional elongation | |
Attenuator type: | Transcriptional |
Strand: | forward |
Structure type | Energy | LeftPos | RightPos | Sequence (RNA-strand) | |
---|---|---|---|---|---|
terminator | -17.1 | 1015480 | 1015517 | tgtaaatataACCGTCTCCGGTATGTTGCCTGAGGCGGTTTTTTTGTctctaacgtg | |
anti-terminator | -3.8 | 1015476 | 1015496 | gatttgtaaaTATAACCGTCTCCGGTATGTtgcctgaggc |
Notes: "The provided "Sequence" is that of the RNA strand, i.e. U's are shown instead of T's and regulators on the reverse strand will appear as the reverse complement of the sequence delimited by LeftPos-RigtPos" |
Reference(s) |
![]() |
---|---|