| RRC ID |
89131
|
| Author |
Akiyama K, Yano K, Niki H.
|
| Title |
Involvement of the inner surface residues of bacterial SMC protein MukB in the ssDNA binding in vitro.
|
| Journal |
Commun Biol
|
| Abstract |
The bacterial condensin MukB facilitates proper chromosome segregation in Escherichia coli. MukB protein localizes at the ori adjacent region by unknown mechanism. The MukB protein entraps the single-stranded DNA (ssDNA) molecule more efficiently than double-stranded DNA (dsDNA). In the bacterial genome, several copies of the rrn genes are encoded near the ori region. The rrn regions are expected to efficiently generate ssDNA due to their high transcriptional activity and the frequent formation of R-loops. In this study, we identified residues involved in DNA binding. The mutations impaired ssDNA binding more severely than dsDNA binding in vitro, and also caused deficiencies in cell growth and nucleoid segregation. These amino acid residues are aligned and are thought to bind DNA when the MukB dimer entraps a DNA molecule within its ring, thereby likely enhancing the DNA-binding activity of MukB. These residues may contribute to the accumulation of MukB on the chromosome, including the rrn regions.
|
| Volume |
9(1)
|
| Pages |
79
|
| Published |
2025-12-16
|
| DOI |
10.1038/s42003-025-09345-5
|
| PII |
10.1038/s42003-025-09345-5
|
| PMID |
41402526
|
| PMC |
PMC12820191
|
| MeSH |
Bacterial Proteins / metabolism
Chromosomal Proteins, Non-Histone* / chemistry
Chromosomal Proteins, Non-Histone* / genetics
Chromosomal Proteins, Non-Histone* / metabolism
DNA, Bacterial / genetics
DNA, Bacterial / metabolism
DNA, Single-Stranded* / genetics
DNA, Single-Stranded* / metabolism
DNA-Binding Proteins* / chemistry
DNA-Binding Proteins* / genetics
DNA-Binding Proteins* / metabolism
Escherichia coli* / genetics
Escherichia coli* / metabolism
Escherichia coli Proteins* / chemistry
Escherichia coli Proteins* / genetics
Escherichia coli Proteins* / metabolism
Mutation
Protein Binding
|
| Resource |
| Prokaryotes E. coli |
|