Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Asymmetric Lipid Bilayer01:35

Asymmetric Lipid Bilayer

9.6K
Biological membranes show uneven distribution of different types of lipids in the inner and outer layers, resulting in transverse asymmetric membranes. The treatment of the erythrocyte membrane with the enzyme phospholipase confirmed the asymmetric nature of the lipid bilayer. The enzyme hydrolyzes lipids into fatty acids and hydrophilic groups. The phospholipase acts only on the outer layer of the membrane, while the inner layer remains intact. The phospholipase treatment resulted in 80%...
9.6K
Mechanisms of Membrane-bending01:15

Mechanisms of Membrane-bending

3.3K
The living membranes are flexible due to their fluid mosaic nature; however, their bending into different shapes is an active process regulated by specific lipids and proteins. The membrane bending can be transient as seen in vesicles or stable for a long time as in microvilli. Cells regulate the size, location, and duration of the membrane curvature.
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
3.3K
Membrane Asymmetry Regulating Transporters01:19

Membrane Asymmetry Regulating Transporters

6.9K
Enzymes like flippase, floppase, and scramblase transfer phospholipids from one layer to another in the membrane, thereby affecting membrane asymmetry.
Flippase
Eukaryotic flippases are type-IV P-type ATPases or P4-ATPases belonging to P-type ATPase family proteins that are membrane-bound pumps involved in the ATP-mediated transport of ions and molecules across the membrane. Flippases flip specific phospholipids from the outer to the inner leaflet of a membrane. All P4-ATPases have one...
6.9K
Enlargement of the Plasma Membrane01:22

Enlargement of the Plasma Membrane

2.2K
Cell division and enlargement are processes that require precise control. The control ensures that cell division cannot proceed unless the cell has grown to a specific size. A spherical, dividing cell requires an approximately 1.6X increase in its surface area to double its volume. The secretory pathway also has a significant role in cell membrane enlargement. Secretory vesicles that bud off from the Golgi apparatus and later fuse with the plasma membrane during exocytosis are a major source of...
2.2K
What are Membranes?01:24

What are Membranes?

18.3K
A cell's plasma membrane demarcates the cell's borders and determines the nature of its interaction with the environment. Cells exclude certain substances, take in others, and excrete some others in controlled quantities. The plasma membrane must be flexible to allow certain cells, such as red and white blood cells, to change their shape while passing through narrow capillaries. These are the more obvious plasma membrane functions. In addition, the plasma membrane's surface carries...
18.3K
What are Membranes?01:54

What are Membranes?

188.0K
A key characteristic of life is the ability to separate the external environment from the internal space. To do this, cells have evolved semi-permeable membranes that regulate the passage of biological molecules. Additionally, the cell membrane defines a cell’s shape and interactions with the external environment. Eukaryotic cell membranes also serve to compartmentalize the internal space into organelles, including the endomembrane structures of the nucleus, endoplasmic reticulum and...
188.0K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Reliable replicative lifespan determination of yeast with a single-channel microfluidic chip.

Biology open·2024
Same author

Discovery of archaeal fusexins homologous to eukaryotic HAP2/GCS1 gamete fusion proteins.

Nature communications·2022
Same author

Scalable phylogenetic profiling using MinHash uncovers likely eukaryotic sexual reproduction genes.

PLoS computational biology·2020
Same journal

Mechanistic insights into acetylated histone recognition by the CECR2 bromodomain.

The Biochemical journal·2026
Same journal

Nanobodies against Plasmodium adhesins that block receptor engagement and malaria parasite invasion.

The Biochemical journal·2026
Same journal

Persistence without turnover: the RhoG G12E mutant highlights the role of nucleotide cycling in RhoG signaling.

The Biochemical journal·2026
Same journal

Alternative Splicing of Rice Chloroplastic CuZn Superoxide Dismutase, OsCSD2: Impact on expression and protein characteristics.

The Biochemical journal·2026
Same journal

Difference and similarity between the ubiquitous secretory pathway Ca2+-ATPases, SERCA2b, and SPCA1a.

The Biochemical journal·2026
Same journal

A molecular perspective on dimethylarginine dimethylaminohydrolases structure and function.

The Biochemical journal·2026
See all related articles

Related Experiment Video

Updated: Jan 15, 2026

Cell Membrane Repair Assay Using a Two-photon Laser Microscope
06:35

Cell Membrane Repair Assay Using a Two-photon Laser Microscope

Published on: January 2, 2018

13.4K

Cell membrane asymmetries and cellular aging.

Valentina Salzman1, Pablo S Aguilar1

  • 1Instituto de FisiologĂ­a, BiologĂ­a Molecular y Neurociencias (IFIBYNE), CONICET, Buenos Aires, C1428EGA, Argentina.

The Biochemical Journal
|October 9, 2025
PubMed
Summary
This summary is machine-generated.

Budding yeast cells reset their lifespan through asymmetric cell division, ensuring daughters inherit full potential. This process relies on membrane proteins that asymmetrically distribute aging factors from mother to daughter cells.

Keywords:
agingasymmetric cell divisionmembraneyeast

More Related Videos

Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions
06:32

Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions

Published on: July 28, 2022

2.6K
A Model Membrane Platform for Reconstituting Mitochondrial Membrane Dynamics
10:31

A Model Membrane Platform for Reconstituting Mitochondrial Membrane Dynamics

Published on: September 2, 2020

8.0K

Related Experiment Videos

Last Updated: Jan 15, 2026

Cell Membrane Repair Assay Using a Two-photon Laser Microscope
06:35

Cell Membrane Repair Assay Using a Two-photon Laser Microscope

Published on: January 2, 2018

13.4K
Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions
06:32

Reconstitution of Septin Assembly at Membranes to Study Biophysical Properties and Functions

Published on: July 28, 2022

2.6K
A Model Membrane Platform for Reconstituting Mitochondrial Membrane Dynamics
10:31

A Model Membrane Platform for Reconstituting Mitochondrial Membrane Dynamics

Published on: September 2, 2020

8.0K

Area of Science:

  • Cellular Biology
  • Aging Research
  • Yeast Genetics

Background:

  • Saccharomyces cerevisiae, a model eukaryote, divides asymmetrically, producing daughter cells with reset lifespans.
  • Cellular aging is linked to asymmetric inheritance of aging factors during budding.
  • Membrane-associated mechanisms are crucial for this asymmetric inheritance.

Purpose of the Study:

  • To compile a comprehensive catalog of asymmetrically distributed membrane proteins in yeast involved in replicative aging.
  • To synthesize existing knowledge on the establishment and maintenance of membrane asymmetry in yeast.
  • To identify gaps in understanding how membrane asymmetry influences cellular aging.

Main Methods:

  • Literature review and synthesis of existing research on yeast cell division and aging.
  • Identification and cataloging of asymmetrically distributed membrane proteins.
  • Analysis of the roles of these proteins in replicative aging.

Main Results:

  • A comprehensive resource of asymmetrically distributed membrane proteins with roles in yeast replicative aging has been compiled.
  • Existing knowledge regarding the establishment and maintenance of membrane asymmetry has been synthesized.
  • Key gaps in understanding the contribution of membrane asymmetry to cellular aging have been identified.

Conclusions:

  • Asymmetric cell division in yeast resets daughter cell lifespan through mechanisms involving membrane proteins.
  • Further research is needed to fully elucidate the role of membrane asymmetry in cellular aging.
  • This review serves as a foundational resource for future studies in yeast aging.