2016
DOI: 10.7554/elife.12821
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HSF-1 activates the ubiquitin proteasome system to promote non-apoptotic developmental cell death in C. elegans

Abstract: Apoptosis is a prominent metazoan cell death form. Yet, mutations in apoptosis regulators cause only minor defects in vertebrate development, suggesting that another developmental cell death mechanism exists. While some non-apoptotic programs have been molecularly characterized, none appear to control developmental cell culling. Linker-cell-type death (LCD) is a morphologically conserved non-apoptotic cell death process operating in Caenorhabditis elegans and vertebrate development, and is therefore a compelli… Show more

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Cited by 23 publications
(36 citation statements)
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“…However, there is now increasing evidence from a number of biological systems that HSF1 is important for diverse “non-stress” conditions including development [26, 40], energy metabolism [27], programmed cell death [41, 42] and carcinogenesis [28, 43]. For these non-heat shock conditions, the transcriptomes regulated by HSF1 are distinct from that of acute heat shock [26, 40].…”
Section: Hsf1 Directs Transcriptional Programs That Are Uncoupled Fromentioning
confidence: 99%
“…However, there is now increasing evidence from a number of biological systems that HSF1 is important for diverse “non-stress” conditions including development [26, 40], energy metabolism [27], programmed cell death [41, 42] and carcinogenesis [28, 43]. For these non-heat shock conditions, the transcriptomes regulated by HSF1 are distinct from that of acute heat shock [26, 40].…”
Section: Hsf1 Directs Transcriptional Programs That Are Uncoupled Fromentioning
confidence: 99%
“…The death of the male linker cell does not involve the ced-3-encoded caspase or other canonical apoptosis pathway genes, but instead uses the heat shock factor HSF-1 and the ubiquitin proteasome system. EGL-20/LIN-44 WNT ligands, LIN-29-mediated transcriptional regulation, and the TIR-1/SEK-1 kinase pathway provide three redundant systems that regulate the positional timing of the male linker cell's death (Abraham et al 2007) (Blum et al 2012;Kinet et al 2016). After the linker cell dies and its corpse is engulfed, one of the proctodeal cells, B.ae(left or right)aav, directly connects the vas deferens' opening to the proctodeal cavity.…”
Section: Sexual Dimorphism In the Hindgut: Sex-specific Development Amentioning
confidence: 99%
“…The LC is born in the L2 stage and leads elongation of the male gonad during the L3 and L4 stages (Schwarz et al, 2012). The cell undergoes non-apoptotic programmed cell death in the late L4 stage (Blum et al, 2012), and the genetic basis for this has been under recent investigation (Blum et al, 2012; Kinet et al, 2016). Live imaging of LC death has been a major challenge in the field, as imaging over >10 hours is required, often through the L4-adult molt.…”
Section: Introductionmentioning
confidence: 99%