ZapA employs a two-pronged mechanism to facilitate Z ring formation in Escherichia coli
Yuanyuan CuiiD, Han Gong, Di YaniD, Hao LiiD, Wenjie Yang, Ying LiiD, Xiangdong CheniD, Joe LutkenhausiD, S Huang, Xinxing YangiD, Shishen DuiD
Abstract
The tubulin-like protein FtsZ assembles into the Z ring which leads to the assembly and activation of the division machinery in most bacteria. ZapA, a widely conserved protein that interacts with FtsZ, plays a pivotal role in organizing FtsZ filaments into a coherent Z ring. Previous studies revealed that ZapA forms a dumbbell-like tetramer that binds cooperatively to FtsZ filaments and aligns them in parallel, leading to the straightening and organization of FtsZ filament bundles. However, how ZapA interacts with FtsZ remains obscure. In this study, we uncover how ZapA interacts with FtsZ to facilitate Z ring formation in Escherichia coli. We find that mutations affecting surface exposed residues at the junction between adjacent FtsZ subunits in a filament as well as in an N-terminal motif of FtsZ weaken its interaction with ZapA in vivo and in vitro, indicating that ZapA binds to these regions of FtsZ. Consistent with this, ZapA prefers FtsZ polymers over monomeric FtsZ molecules and site-specific crosslinking confirmed that the dimer head domain of ZapA is in contact with the junction of FtsZ subunits. As a result, disruption of the putative interaction interfaces between FtsZ and ZapA abolishes the midcell localization of ZapA. Taken together, our results suggest that ZapA tetramers grab the N-terminal tails of FtsZ and then bind to the junctions between FtsZ subunits in the filament to straighten and crosslink parallel FtsZ filaments into the Z ring. SignificanceZapA is a widely conserved FtsZ-associated protein that promotes the organization of the Z ring, the key cytoskeletal element in the bacterial divisome. Although ZapA is known to crosslink FtsZ filaments, how it interacts with FtsZ remains enigmatic. In this study, we find that E. coli ZapA utilizes a dual binding mode in which it binds the junction between FtsZ subunits in a filament and to an N-terminal motif in FtsZ so that it can straighten and crosslink parallel FtsZ filaments simultaneously. Since the junction is formed when FtsZ polymerizes and falls apart when FtsZ depolymerizes, this interaction mode indicates that ZapA employs the polymerization dynamics of FtsZ to organize the filaments into the Z ring.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 1
- FWCI
- 0.52
- Field percentile
- top 31%
- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- ZapC crosslinks FtsZ filaments through a dual-binding mechanism modulated by the intrinsically disordered linker of FtsZ
Ying Li, Han Gong, … Shishen Du·bioRxiv·May 7, 2025
- Structural basis for the interaction between the bacterial cell division proteins FtsZ and ZapA
Junso Fujita, Kazuki Kasai, … Hiroyoshi Matsumura·Nature CommunicationsPeer-reviewed·Jul 1, 2025
- Escherichia coli ZipA organizes FtsZ polymers into dynamic ring-like protofilament structures
W. Margolin, M. Krupka, … G. Rivas·bioRxiv·May 14, 2018
- Crosslinking by ZapD drives the assembly of short FtsZ filaments into toroidal structures in solution
A. Merino-Salomon, J. Schneider, … G. Rivas·bioRxiv·Jan 12, 2023
- Coregulated assembly of actin-like FtsA polymers with FtsZ during Z-ring formation and division in Escherichia coli
J. J. Morrison, J. Conti, J. L. Camberg·bioRxiv·Jan 12, 2021
- ZapA tetramerization is required for midcell localization and ZapB interaction in Escherichia coli
N. Y. Meiresonne, T. den Blaauwen·bioRxiv·Aug 29, 2019