Matches in SemOpenAlex for { <https://semopenalex.org/work/W2022100907> ?p ?o ?g. }
- W2022100907 endingPage "760" @default.
- W2022100907 startingPage "748" @default.
- W2022100907 abstract "The human lymphocyte toxins granzyme B (hGrzB) and perforin cooperatively induce apoptosis of virus-infected or transformed cells: perforin pores enable entry of the serine protease hGrzB into the cytosol, where it processes Bid to selectively activate the intrinsic apoptosis pathway. Truncated Bid (tBid) induces Bax/Bak-dependent mitochondrial outer membrane permeability and the release of cytochrome c and Smac/Diablo. To identify cellular proteins that regulate perforin/hGrzB-mediated Bid cleavage and subsequent apoptosis, we performed a gene-knockdown (KD) screen using a lentiviral pool of short hairpin RNAs embedded within a miR30 backbone (shRNAmiR). We transduced HeLa cells with a lentiviral pool expressing shRNAmiRs that target 1213 genes known to be involved in cell death signaling and selected cells with acquired resistance to perforin/hGrzB-mediated apoptosis. Twenty-two shRNAmiRs were identified in the positive-selection screen including two, PCAF and ADA3, whose gene products are known to reside in the same epigenetic regulatory complexes. Small interfering (si)RNA-mediated gene-KD of PCAF or ADA3 also conferred resistance to perforin/hGrzB-mediated apoptosis providing independent validation of the screen results. Mechanistically, PCAF and ADA3 exerted their pro-apoptotic effect upstream of mitochondrial membrane permeabilization, as indicated by reduced cytochrome c release in PCAF-KD cells exposed to perforin/hGrzB. While overall levels of Bid were unaltered, perforin/hGrzB-mediated cleavage of Bid was reduced in PCAF-KD or ADA3-KD cells. We discovered that PCAF-KD or ADA3-KD resulted in reduced expression of PACS2, a protein implicated in Bid trafficking to mitochondria and importantly, targeted PACS2-KD phenocopied the effect of PCAF-KD or ADA3-KD. We conclude that PCAF and ADA3 regulate Bid processing via PACS2, to modulate the mitochondrial cell death pathway in response to hGrzB." @default.
- W2022100907 created "2016-06-24" @default.
- W2022100907 creator A5001165148 @default.
- W2022100907 creator A5002951761 @default.
- W2022100907 creator A5004454968 @default.
- W2022100907 creator A5036417435 @default.
- W2022100907 creator A5037071541 @default.
- W2022100907 creator A5040335760 @default.
- W2022100907 creator A5044516621 @default.
- W2022100907 creator A5052829828 @default.
- W2022100907 creator A5064650798 @default.
- W2022100907 date "2014-01-24" @default.
- W2022100907 modified "2023-10-06" @default.
- W2022100907 title "A functional genomics screen identifies PCAF and ADA3 as regulators of human granzyme B-mediated apoptosis and Bid cleavage" @default.
- W2022100907 cites W1948155768 @default.
- W2022100907 cites W1966291495 @default.
- W2022100907 cites W1966969821 @default.
- W2022100907 cites W1973109581 @default.
- W2022100907 cites W1987702938 @default.
- W2022100907 cites W1995926647 @default.
- W2022100907 cites W1997586085 @default.
- W2022100907 cites W2002057703 @default.
- W2022100907 cites W2003137211 @default.
- W2022100907 cites W2004391198 @default.
- W2022100907 cites W2006419043 @default.
- W2022100907 cites W2006981341 @default.
- W2022100907 cites W2010105460 @default.
- W2022100907 cites W2020490276 @default.
- W2022100907 cites W2023075010 @default.
- W2022100907 cites W2023661503 @default.
- W2022100907 cites W2027396500 @default.
- W2022100907 cites W2028526641 @default.
- W2022100907 cites W2033482909 @default.
- W2022100907 cites W2033807824 @default.
- W2022100907 cites W2037485296 @default.
- W2022100907 cites W2041999543 @default.
- W2022100907 cites W2046833816 @default.
- W2022100907 cites W2048607411 @default.
- W2022100907 cites W2063639409 @default.
- W2022100907 cites W2064706357 @default.
- W2022100907 cites W2067322705 @default.
- W2022100907 cites W2078565981 @default.
- W2022100907 cites W2080559728 @default.
- W2022100907 cites W2080915541 @default.
- W2022100907 cites W2081848012 @default.
- W2022100907 cites W2087593127 @default.
- W2022100907 cites W2088474136 @default.
- W2022100907 cites W2092967259 @default.
- W2022100907 cites W2094629286 @default.
- W2022100907 cites W2095217266 @default.
- W2022100907 cites W2098609440 @default.
- W2022100907 cites W2103699489 @default.
- W2022100907 cites W2106526289 @default.
- W2022100907 cites W2109956888 @default.
- W2022100907 cites W2110077740 @default.
- W2022100907 cites W2110396981 @default.
- W2022100907 cites W2113505777 @default.
- W2022100907 cites W2116393840 @default.
- W2022100907 cites W2117316674 @default.
- W2022100907 cites W2119502441 @default.
- W2022100907 cites W2121445223 @default.
- W2022100907 cites W2123600404 @default.
- W2022100907 cites W2133898735 @default.
- W2022100907 cites W2158575103 @default.
- W2022100907 cites W2164296948 @default.
- W2022100907 cites W2166219468 @default.
- W2022100907 cites W2166802464 @default.
- W2022100907 cites W2168001629 @default.
- W2022100907 cites W2170243414 @default.
- W2022100907 cites W2320870975 @default.
- W2022100907 cites W2322040583 @default.
- W2022100907 doi "https://doi.org/10.1038/cdd.2013.203" @default.
- W2022100907 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3978306" @default.
- W2022100907 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24464226" @default.
- W2022100907 hasPublicationYear "2014" @default.
- W2022100907 type Work @default.
- W2022100907 sameAs 2022100907 @default.
- W2022100907 citedByCount "14" @default.
- W2022100907 countsByYear W20221009072014 @default.
- W2022100907 countsByYear W20221009072015 @default.
- W2022100907 countsByYear W20221009072016 @default.
- W2022100907 countsByYear W20221009072017 @default.
- W2022100907 countsByYear W20221009072018 @default.
- W2022100907 countsByYear W20221009072019 @default.
- W2022100907 countsByYear W20221009072020 @default.
- W2022100907 countsByYear W20221009072021 @default.
- W2022100907 countsByYear W20221009072022 @default.
- W2022100907 crossrefType "journal-article" @default.
- W2022100907 hasAuthorship W2022100907A5001165148 @default.
- W2022100907 hasAuthorship W2022100907A5002951761 @default.
- W2022100907 hasAuthorship W2022100907A5004454968 @default.
- W2022100907 hasAuthorship W2022100907A5036417435 @default.
- W2022100907 hasAuthorship W2022100907A5037071541 @default.
- W2022100907 hasAuthorship W2022100907A5040335760 @default.
- W2022100907 hasAuthorship W2022100907A5044516621 @default.
- W2022100907 hasAuthorship W2022100907A5052829828 @default.
- W2022100907 hasAuthorship W2022100907A5064650798 @default.
- W2022100907 hasBestOaLocation W20221009072 @default.