Membrane fission during bacterial spore development requires cellular inflation driven by DNA translocation.
Membrane fission during bacterial spore development requires cellular inflation driven by DNA translocation.
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DOI:
10.1016/j.cub.2022.08.014
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发表时间:
2022-10-10
期刊:
影响因子:
9.2
通讯作者:
Karatekin, Erdem
中科院分区:
文献类型:
--
作者:
Landajuela, Ane;Braun, Martha;Martinez-Calvo, Alejandro;Rodrigues, Christopher D. A.;Perez, Carolina Gomis;Doan, Thierry;Rudner, David Z.;Wingreen, Ned S.;Karatekin, Erdem
Bacteria require membrane fission for both cell division and endospore formation. In Bacillus subtilis, sporulation initiates with an asymmetric division that generates a large mother cell and a smaller forespore that contains only a quarter of its genome. As the mother cell membranes engulf the forespore, a DNA translocase pumps the rest of the chromosome into the small forespore compartment, inflating it due to increased turgor. When the engulfing membrane undergoes fission, the forespore is released into the mother cell cytoplasm. The B. subtilis protein FisB catalyzes membrane fission during sporulation, but the molecular basis is unclear. Here we show that forespore inflation and FisB accumulation are both required for efficient membrane fission. Forespore inflation leads to higher membrane tension in the engulfment membrane than in the mother cell membrane, causing membrane to flow through the neck connecting the two membrane compartments. Thus, the mother cell supplies some of the membrane required for the growth of the membranes surrounding the forespore. Oligomerization of FisB at the membrane neck slows equilibration of membrane tension by impeding membrane flow. This leads to a further increase in the tension of the engulfment membrane, promoting its fission through lysis. Collectively our data indicate that DNA-translocation has a previously unappreciated second function in energizing FisB-mediated membrane fission under energy-limited conditions. Landajuela et al. show that fission of a membrane neck during endospore formation in Bacillus subtilis results from an interplay between increasing membrane tension on one side of the neck and accumulation of a cluster of FisB proteins inside it, impeding membrane flux and tension equilibration.
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