RhoA regulation in space and time. Issue 6 (29th January 2023)
- Record Type:
- Journal Article
- Title:
- RhoA regulation in space and time. Issue 6 (29th January 2023)
- Main Title:
- RhoA regulation in space and time
- Authors:
- de Seze, Jean
Gatin, Joséphine
Coppey, Mathieu - Other Names:
- Cherfils Jacqueline guestEditor.
- Abstract:
- Abstract : RhoGTPases are well known for being controllers of cell cytoskeleton and share common features in the way they act and are controlled. These include their switch from GDP to GTP states, their regulations by different guanine exchange factors (GEFs), GTPase‐activating proteins and guanosine dissociation inhibitors (GDIs), and their similar structure of active sites/membrane anchors. These very similar features often lead to the common consideration that the differences in their biological effects mainly arise from the different types of regulators and specific effectors associated with each GTPase. Focusing on data obtained through biosensors, live cell microscopy and recent optogenetic approaches, we highlight in this review that the regulation of RhoA appears to depart from Cdc42 and Rac1 modes of regulation through its enhanced lability at the plasma membrane. RhoA presents a high dynamic turnover at the membrane that is regulated not only by GDIs but also by GEFs, effectors and a possible soluble conformational state. This peculiarity of RhoA regulation may be important for the specificities of its functions, such as the existence of activity waves or its putative dual role in the initiation of protrusions and contractions. Abstract : RhoA is a key regulator of cell cytoskeleton dynamics, usually described as a simple switch residing at the plasma membrane. In this review, we show that the highly diverse patterns of RhoA activity call for additional layers ofAbstract : RhoGTPases are well known for being controllers of cell cytoskeleton and share common features in the way they act and are controlled. These include their switch from GDP to GTP states, their regulations by different guanine exchange factors (GEFs), GTPase‐activating proteins and guanosine dissociation inhibitors (GDIs), and their similar structure of active sites/membrane anchors. These very similar features often lead to the common consideration that the differences in their biological effects mainly arise from the different types of regulators and specific effectors associated with each GTPase. Focusing on data obtained through biosensors, live cell microscopy and recent optogenetic approaches, we highlight in this review that the regulation of RhoA appears to depart from Cdc42 and Rac1 modes of regulation through its enhanced lability at the plasma membrane. RhoA presents a high dynamic turnover at the membrane that is regulated not only by GDIs but also by GEFs, effectors and a possible soluble conformational state. This peculiarity of RhoA regulation may be important for the specificities of its functions, such as the existence of activity waves or its putative dual role in the initiation of protrusions and contractions. Abstract : RhoA is a key regulator of cell cytoskeleton dynamics, usually described as a simple switch residing at the plasma membrane. In this review, we show that the highly diverse patterns of RhoA activity call for additional layers of regulation: RhoA residence time at the plasma membrane, localization in space and time, and positive/negative feedback loops. … (more)
- Is Part Of:
- FEBS letters. Volume 597:Issue 6(2023)
- Journal:
- FEBS letters
- Issue:
- Volume 597:Issue 6(2023)
- Issue Display:
- Volume 597, Issue 6 (2023)
- Year:
- 2023
- Volume:
- 597
- Issue:
- 6
- Issue Sort Value:
- 2023-0597-0006-0000
- Page Start:
- 836
- Page End:
- 849
- Publication Date:
- 2023-01-29
- Subjects:
- biosensor -- membrane signalling -- optogenetics -- regulation -- RhoA -- Rho‐GTPases -- signalling waves
Biochemistry -- Periodicals
Biophysics -- Periodicals
Molecular biology -- Periodicals
Biochimie -- Périodiques
Biochemistry
Biophysics
Molecular biology
Periodicals
572.05 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00145793 ↗
http://febs.onlinelibrary.wiley.com/hub/journal/10.1002/(ISSN)1873-3468/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1002/1873-3468.14578 ↗
- Languages:
- English
- ISSNs:
- 0014-5793
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3901.600000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 26621.xml