Altruistic feeding and cell-cell signaling during bacterial differentiation actively enhance phenotypic heterogeneity.


Journal

Science advances
ISSN: 2375-2548
Titre abrégé: Sci Adv
Pays: United States
ID NLM: 101653440

Informations de publication

Date de publication:
18 Oct 2024
Historique:
medline: 18 10 2024
pubmed: 18 10 2024
entrez: 18 10 2024
Statut: ppublish

Résumé

Starvation triggers bacterial spore formation, a committed differentiation program that transforms a vegetative cell into a dormant spore. Cells in a population enter sporulation nonuniformly to secure against the possibility that favorable growth conditions, which put sporulation-committed cells at a disadvantage, may resume. This heterogeneous behavior is initiated by a passive mechanism: stochastic activation of a master transcriptional regulator. Here, we identify a cell-cell communication pathway containing the proteins ShfA (YabQ) and ShfP (YvnB) that actively promotes phenotypic heterogeneity, wherein

Identifiants

pubmed: 39423260
doi: 10.1126/sciadv.adq0791
doi:

Substances chimiques

Bacterial Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

eadq0791

Auteurs

Taylor B Updegrove (TB)

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Thomas Delerue (T)

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Vivek Anantharaman (V)

Computational Biology Branch, Division of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.

Hyomoon Cho (H)

Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

Carissa Chan (C)

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Thomas Nipper (T)

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Hyoyoung Choo-Wosoba (H)

Office of Collaborative Biostatistics, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Lisa M Jenkins (LM)

Laboratory of Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

Lixia Zhang (L)

Advanced Imaging and Microscopy Resource, National Institutes of Health, Bethesda, MD, USA.

Yijun Su (Y)

Laboratory of High Resolution Optical Imaging, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, USA.
Janelia Farm Research Campus, Howard Hughes Medical Institute (HHMI), Ashburn, VA, USA.

Hari Shroff (H)

Laboratory of High Resolution Optical Imaging, National Institute of Biomedical Imaging and Bioengineering, National Institutes of Health, Bethesda, MD, USA.
Janelia Farm Research Campus, Howard Hughes Medical Institute (HHMI), Ashburn, VA, USA.

Jiji Chen (J)

Advanced Imaging and Microscopy Resource, National Institutes of Health, Bethesda, MD, USA.

Carole A Bewley (CA)

Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD, USA.

L Aravind (L)

Computational Biology Branch, Division of Intramural Research, National Library of Medicine, National Institutes of Health, Bethesda, MD, USA.

Kumaran S Ramamurthi (KS)

Laboratory of Molecular Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.

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Classifications MeSH