2008
DOI: 10.1016/j.cyto.2008.07.029
|View full text |Cite
|
Sign up to set email alerts
|

PL-7 Mechanism of foreign RNA recognition in the cytoplasm

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

1
2
0

Year Published

2016
2016
2022
2022

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 0 publications
1
2
0
Order By: Relevance
“…The 5′-triphosphate of RNA plays a role in the recognition of pathogenic RNA genomes by RIG-I. 25 We confirmed that calf intestinal alkaline phosphatase (CIAP)-treated IVT-B2 RNA lost the capability of inducing RIG-I/MAVS-related downstream Noxa and TRAIL expression (Supplementary Figure S7a) and IFN-β secretion in PC3 cells (Supplementary Figure S7b). These results suggested that both the double-stranded stem region and 5′-triphosphate of IVT-B2 are crucial in inducing the RIG-I/ MAVS-related downstream anticancer effects.…”
Section: Ivt-di Rna-induced Cancer Cell Death and The Expression Of Apoptosis-related Proteins In Pc3 Cellssupporting
confidence: 55%
“…The 5′-triphosphate of RNA plays a role in the recognition of pathogenic RNA genomes by RIG-I. 25 We confirmed that calf intestinal alkaline phosphatase (CIAP)-treated IVT-B2 RNA lost the capability of inducing RIG-I/MAVS-related downstream Noxa and TRAIL expression (Supplementary Figure S7a) and IFN-β secretion in PC3 cells (Supplementary Figure S7b). These results suggested that both the double-stranded stem region and 5′-triphosphate of IVT-B2 are crucial in inducing the RIG-I/ MAVS-related downstream anticancer effects.…”
Section: Ivt-di Rna-induced Cancer Cell Death and The Expression Of Apoptosis-related Proteins In Pc3 Cellssupporting
confidence: 55%
“…The C-terminal domain (CTD) consists of four conserved cysteines (C810, C813, C864, C869) linked by zinc or, less commonly, a mercury atom. These are the major structural and functional components of this protein that is responsible for transmitting the signal that activates the antiviral response by binding dsRNA and ssRNA 5'-triphosphate (23,24). The activation of RIG-I receptor expression is only possible when the appropriate ligand interacts with the CTD domain (9).…”
Section: Rig-i-like Receptorsmentioning
confidence: 99%
“…Retinoic acid-induced gene I (RIG-I) is a cytosolic receptor that senses double-stranded RNA (dsRNA) originating from pathogens such as viruses (2)(3)(4)(5). Binding to dsRNA disrupts an intramolecular interaction that keeps RIG-I in an autoinhibitory state (6,7), triggering an overall conformational change that releases the N-terminal CARD domain (8, 9). The N-terminal CARD of RIG-I undergoes homotypic oligomerization and heterooligomerization with that of the mitochondrion antiviral signaling (MAVS) adaptor molecule (10).…”
mentioning
confidence: 99%