• HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
Thursday, August 28, 2025
BIOENGINEER.ORG
No Result
View All Result
  • Login
  • HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
        • Lecturer
        • PhD Studentship
        • Postdoc
        • Research Assistant
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
  • HOME
  • NEWS
  • EXPLORE
    • CAREER
      • Companies
      • Jobs
        • Lecturer
        • PhD Studentship
        • Postdoc
        • Research Assistant
    • EVENTS
    • iGEM
      • News
      • Team
    • PHOTOS
    • VIDEO
    • WIKI
  • BLOG
  • COMMUNITY
    • FACEBOOK
    • INSTAGRAM
    • TWITTER
No Result
View All Result
Bioengineer.org
No Result
View All Result
Home NEWS Science News Biology

Phase separation of scaffold protein regulates microbial asymmetric cell division

Bioengineer by Bioengineer
December 13, 2022
in Biology
Reading Time: 2 mins read
0
Share on FacebookShare on TwitterShare on LinkedinShare on RedditShare on Telegram

By polarizing different cell fate determinants at opposite cell poles, asymmetric cell division (ACD) that produces distinct daughter cells is an evolutionarily conserved mechanism to generate cellular diversity in both eukaryotes and prokaryotes. 

Distinct signaling hubs localized at the opposite cell poles in C. crescentus

Credit: SIAT

By polarizing different cell fate determinants at opposite cell poles, asymmetric cell division (ACD) that produces distinct daughter cells is an evolutionarily conserved mechanism to generate cellular diversity in both eukaryotes and prokaryotes. 

The polarization of the scaffold-signaling hubs at cell poles constitutes the basis of ACD. However, the biomolecular basis and regulatory mechanism of the polar signaling complexes has been largely unclear.

Recently, a research team led by Prof. ZHAO Wei from the Shenzhen Institute of Advanced Technology (SIAT) of the Chinese Academy of Sciences proposed that the polar organelle development scaffold protein PodJ in the new cell pole forms biomolecular condensates with physiological functions via phase separation, which help to establish and regulate the asymmetry of bacterial cells.

The study was published in Nature Communications on Nov. 23.

As a well-established model for studying bacterial ACD, Caulobacter crescentus produces a motile swarmer cell and a sessile stalked cell during each cell cycle. In the pre-division cell stage, the polarization of new-pole signaling proteins by the scaffold PodJ coordinates to modulate the phosphorylation levels of a set of downstream signaling proteins, thus determining the cell fate of C. crescentus.

The researchers found that phase separation played an essential role in the C. crescentus PodJ-signaling hub assembly. PodJ formed biomolecular condensates both in vitro and in vivo. Either the coiled-coil 4–6 region or the intrinsically disordered region in PodJ could mediate PodJ phase separation. In addition, both of the phase separation-related domains were found to be involved in recruiting client signaling proteins, indicating that phase separation of PodJ functionally contributes to forming the PodJ–client complexes.

Moreover, a negative regulation of PodJ phase separation by the old-cell-pole scaffold protein SpmX was observed. SpmX inhibited PodJ condensate formation and promoted PodJ condensate aging in vitro. In living cells, SpmX was found to impede the cell-pole accumulation of PodJ and client recruitment, suggesting it may be involved in the new-to-old cell-pole remodeling.

“The results revealed that phase separation modulates the assembly and dynamics of scaffold-signaling hubs in C. crescentus,” said Prof. ZHAO Wei, corresponding author of the study. “It may serve as a general biophysical approach for assembling scaffold-signaling complexes and regulating ACD. Similar methods could be employed for rational engineering of artificial organelles and other membraneless biocatalytic compartments.”



Journal

Nature Communications

DOI

10.1038/s41467-022-35000-2

Article Title

Phase separation modulates the assembly and dynamics of a polarity-related scaffold-signaling hub

Article Publication Date

23-Nov-2022

Share12Tweet8Share2ShareShareShare2

Related Posts

Ferroptosis Links to Acute Kidney Disease Genes

Ferroptosis Links to Acute Kidney Disease Genes

August 28, 2025
Red Beet Gene Boosts Tuber Growth and Disease Resistance

Red Beet Gene Boosts Tuber Growth and Disease Resistance

August 28, 2025

VHL Inhibits Angiogenesis via HIF-1a in Macrophages

August 28, 2025

Trainer Insights on Canine Aggression and Behavior Solutions

August 27, 2025

POPULAR NEWS

  • blank

    Breakthrough in Computer Hardware Advances Solves Complex Optimization Challenges

    149 shares
    Share 60 Tweet 37
  • Molecules in Focus: Capturing the Timeless Dance of Particles

    142 shares
    Share 57 Tweet 36
  • New Drug Formulation Transforms Intravenous Treatments into Rapid Injections

    115 shares
    Share 46 Tweet 29
  • Neuropsychiatric Risks Linked to COVID-19 Revealed

    82 shares
    Share 33 Tweet 21

About

We bring you the latest biotechnology news from best research centers and universities around the world. Check our website.

Follow us

Recent News

Ferroptosis Links to Acute Kidney Disease Genes

Transforming Biomedical Engineering Education in the Philippines

TLR4 Polymorphisms Increase Risk in CMV-Positive Pregnancies

  • Contact Us

Bioengineer.org © Copyright 2023 All Rights Reserved.

Welcome Back!

Login to your account below

Forgotten Password?

Retrieve your password

Please enter your username or email address to reset your password.

Log In
No Result
View All Result
  • Homepages
    • Home Page 1
    • Home Page 2
  • News
  • National
  • Business
  • Health
  • Lifestyle
  • Science

Bioengineer.org © Copyright 2023 All Rights Reserved.