1990
DOI: 10.1016/0896-6273(90)90080-y
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Activation of polyubiquitin gene expression during developmentally programmed cell death

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Cited by 199 publications
(129 citation statements)
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“…This induction is more rapid than that of mdm-2, in agreement with the pro- Table 1 Expression of genes indentified by their diffential expression during apoptosis Gene(s) Induced in Expression in REtsAF Calmodulin, chondroitin sulfate Glucocorticoids induced thymocyte apoptosis [11,20] Not detected proteoglycan core protein RP8 Glutathione S-transferase Ybl Clusterin Ubiquitin Glucocorticoids or radiation induced thymocyte apoptosis [15] Prostate regression [32] and steroid induced lymphocyte apoptosis [21] Prostate regression and various other cell death process [17] Radiation-induced lymphocyte apoptosis [18] and insect muscles degeneration [19] [29], which suggest that, in some cells, p53 can mediate apoptosis by repressing survival genes. Recently, a reevaluation of the role of de novo protein synthesis in thymocyte apoptosis has also suggested that inhibitors of protein synthesis may delay apoptosis rather than prevent it [30], suggesting that some of the components of the apoptotic machinery are already present before apoptosis induction.…”
Section: Discussionsupporting
confidence: 64%
See 1 more Smart Citation
“…This induction is more rapid than that of mdm-2, in agreement with the pro- Table 1 Expression of genes indentified by their diffential expression during apoptosis Gene(s) Induced in Expression in REtsAF Calmodulin, chondroitin sulfate Glucocorticoids induced thymocyte apoptosis [11,20] Not detected proteoglycan core protein RP8 Glutathione S-transferase Ybl Clusterin Ubiquitin Glucocorticoids or radiation induced thymocyte apoptosis [15] Prostate regression [32] and steroid induced lymphocyte apoptosis [21] Prostate regression and various other cell death process [17] Radiation-induced lymphocyte apoptosis [18] and insect muscles degeneration [19] [29], which suggest that, in some cells, p53 can mediate apoptosis by repressing survival genes. Recently, a reevaluation of the role of de novo protein synthesis in thymocyte apoptosis has also suggested that inhibitors of protein synthesis may delay apoptosis rather than prevent it [30], suggesting that some of the components of the apoptotic machinery are already present before apoptosis induction.…”
Section: Discussionsupporting
confidence: 64%
“…Three types of genes were studied: (1) genes identified during glucocorticoid-induced thymocyte apoptosis (RP-8) [11,15]; (2) during prostate regression and other cell-death processes (clusterin) [17]; and (3) during y irradiation-induced lymphocyte apoptosis [18] and insect muscle degeneration [19] (polyubiquitin). Fig.…”
Section: Expression Of Genes Induced During Apoptosis In Other Systemsmentioning
confidence: 99%
“…2g), a marker for epithelial-mesenchymal transformation and cell migration (Wunsch and Hass, 1995). Alternatively, the conjugated form of ubiquitin is a known component of cell death pathways in development (Schwartz et al, 1990). The positive staining in the midline may also indicate regulated cell death, giving rise to the cell fragments detected along the primitive groove.…”
Section: Identification Of Midline Cellsmentioning
confidence: 99%
“…Emerging evidence suggests a role for the ubiquitin system in selective developmental processes (Pickart et al, 1989;Schwartz et al, 1990;Glotzer et al, 1991;Scotting et al, 1991;Muralidhar and Thomas, 1993;Haas et al, 1995). We have therefore taken the first systematic approach towards identifying and characterizing ubiquitin and its associated enzymes in early development using a single vertebrate animal model.…”
Section: Discussionmentioning
confidence: 99%
“…The restricted expression of ben to the nervous system during development suggests a role for ubiquitin-mediated protein modification in nervous system development, including growth cone guidance (Muralidhar and Thomas, 1993;Oh et al, 1994). Studies have demonstrated a role for ubiquitin in the degeneration of the intersegmental muscles (ISM) following pupation in the tobacco hawkmoth, Manduca sexta (Schwartz et al, 1990). Subsequently, it was revealed that a 10-fold increase in ISM ubiquitin-conjugate levels, under the regulation of glucocorticoid 20-hydroxyecdysone, is responsible for the ISM developmentally programmed cell death (Haas et al, 1995).…”
Section: Introductionmentioning
confidence: 99%