Combining genetic and biophysical approaches to probe the structure and function relationships of the notch receptor. (17th February 2017)
- Record Type:
- Journal Article
- Title:
- Combining genetic and biophysical approaches to probe the structure and function relationships of the notch receptor. (17th February 2017)
- Main Title:
- Combining genetic and biophysical approaches to probe the structure and function relationships of the notch receptor
- Authors:
- Baron, Martin
- Abstract:
- Abstract: Notch is a conserved cell signalling receptor regulating many aspects of development and tissue homeostasis. Notch is activated by ligand-induced proteolytic cleavages that release the Notch intracellular domain, which relocates to the nucleus to regulate gene transcription. Proteolytic activation first requires mechanical force to be applied to the Notch extracellular domain through an endocytic pulling mechanism transmitted through the ligand/receptor interface. This exposes the proteolytic cleavage site allowing the signal to be initiated following removal of the Notch extracellular domain. Ligands can also act, when expressed in the same cell, through non-productive cis-interactions to inhibit Notch activity. Furthermore, ligand selectivity and Notch activation are regulated by numerous post-translational modifications of the extracellular domain. Additional non-canonical trans and cis interactions with other regulatory proteins may modulate alternative mechanisms of Notch activation that depend on endocytic trafficking of the full-length receptor and proteolytic release of the intracellular domain from endo-lysosomal surface. Mutations of Notch, located in different regions of the protein, are associated with a spectrum of different loss and gain of function phenotypes and offer the possibility to dissect distinct regulatory interactions and mechanisms, particularly when combined with detailed structural analysis of Notch in complex with various regulatoryAbstract: Notch is a conserved cell signalling receptor regulating many aspects of development and tissue homeostasis. Notch is activated by ligand-induced proteolytic cleavages that release the Notch intracellular domain, which relocates to the nucleus to regulate gene transcription. Proteolytic activation first requires mechanical force to be applied to the Notch extracellular domain through an endocytic pulling mechanism transmitted through the ligand/receptor interface. This exposes the proteolytic cleavage site allowing the signal to be initiated following removal of the Notch extracellular domain. Ligands can also act, when expressed in the same cell, through non-productive cis-interactions to inhibit Notch activity. Furthermore, ligand selectivity and Notch activation are regulated by numerous post-translational modifications of the extracellular domain. Additional non-canonical trans and cis interactions with other regulatory proteins may modulate alternative mechanisms of Notch activation that depend on endocytic trafficking of the full-length receptor and proteolytic release of the intracellular domain from endo-lysosomal surface. Mutations of Notch, located in different regions of the protein, are associated with a spectrum of different loss and gain of function phenotypes and offer the possibility to dissect distinct regulatory interactions and mechanisms, particularly when combined with detailed structural analysis of Notch in complex with various regulatory partners. … (more)
- Is Part Of:
- Molecular membrane biology. Volume 34:Number 1/2(2017)
- Journal:
- Molecular membrane biology
- Issue:
- Volume 34:Number 1/2(2017)
- Issue Display:
- Volume 34, Issue 1/2 (2017)
- Year:
- 2017
- Volume:
- 34
- Issue:
- 1/2
- Issue Sort Value:
- 2017-0034-NaN-0000
- Page Start:
- 33
- Page End:
- 49
- Publication Date:
- 2017-02-17
- Subjects:
- Notch -- EGF-module -- cell signalling -- endocytosis -- mechano-transduction
Membranes (Biology) -- Periodicals
Biochemistry -- Periodicals
Cell membranes -- Periodicals
Molecular biology -- Periodicals
571.64 - Journal URLs:
- http://informahealthcare.com/loi/mbc ↗
http://informahealthcare.com ↗ - DOI:
- 10.1080/09687688.2018.1503742 ↗
- Languages:
- English
- ISSNs:
- 0968-7688
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817955
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 7997.xml