| Id |
Subject |
Object |
Predicate |
Lexical cue |
| T1 |
0-104 |
Sentence |
denotes |
Characterization of a mutant cell line that does not activate NF-kappaB in response to multiple stimuli. |
| T1 |
0-104 |
Sentence |
denotes |
Characterization of a mutant cell line that does not activate NF-kappaB in response to multiple stimuli. |
| T2 |
105-255 |
Sentence |
denotes |
Numerous genes required during the immune or inflammation response as well as the adhesion process are regulated by nuclear factor kappaB (NF-kappaB). |
| T2 |
105-255 |
Sentence |
denotes |
Numerous genes required during the immune or inflammation response as well as the adhesion process are regulated by nuclear factor kappaB (NF-kappaB). |
| T3 |
256-352 |
Sentence |
denotes |
Associated with its inhibitor, I kappaB, NF-kappaB resides as an inactive form in the cytoplasm. |
| T3 |
256-352 |
Sentence |
denotes |
Associated with its inhibitor, I kappaB, NF-kappaB resides as an inactive form in the cytoplasm. |
| T4 |
353-492 |
Sentence |
denotes |
Upon stimulation by various agents, I kappaB is proteolyzed and NF-kappaB translocates to the nucleus, where it activates its target genes. |
| T4 |
353-492 |
Sentence |
denotes |
Upon stimulation by various agents, I kappaB is proteolyzed and NF-kappaB translocates to the nucleus, where it activates its target genes. |
| T5 |
493-579 |
Sentence |
denotes |
The transduction pathways that lead to I kappaB inactivation remain poorly understood. |
| T5 |
493-579 |
Sentence |
denotes |
The transduction pathways that lead to I kappaB inactivation remain poorly understood. |
| T6 |
580-748 |
Sentence |
denotes |
In this study, we have characterized a cellular mutant, the 70/Z3-derived 1.3E2 murine pre-B cell line, that does not activate NF-kappaB in response to several stimuli. |
| T6 |
580-748 |
Sentence |
denotes |
In this study, we have characterized a cellular mutant, the 70/Z3-derived 1.3E2 murine pre-B cell line, that does not activate NF-kappaB in response to several stimuli. |
| T7 |
749-988 |
Sentence |
denotes |
We demonstrate that upon stimulation by lipopolysaccharide, Taxol, phorbol myristate acetate, interleukin-1, or double-stranded RNA, I kappaB alpha is not degraded, as a result of an absence of induced phosphorylation on serines 32 and 36. |
| T7 |
749-988 |
Sentence |
denotes |
We demonstrate that upon stimulation by lipopolysaccharide, Taxol, phorbol myristate acetate, interleukin-1, or double-stranded RNA, I kappaB alpha is not degraded, as a result of an absence of induced phosphorylation on serines 32 and 36. |
| T8 |
989-1153 |
Sentence |
denotes |
Neither a mutation in I kappaB alpha nor a mutation in p50 or relA, the two major subunits of NF-kappaB in this cell line, accounts for this phosphorylation defect. |
| T8 |
989-1153 |
Sentence |
denotes |
Neither a mutation in I kappaB alpha nor a mutation in p50 or relA, the two major subunits of NF-kappaB in this cell line, accounts for this phosphorylation defect. |
| T9 |
1154-1375 |
Sentence |
denotes |
As well as culminating in the inducible phosphorylation of I kappaB alpha on serines 32 and 36, all the stimuli that are inactive on 1.3E2 cells exhibit a sensitivity to the antioxidant pyrrolidine dithiocarbamate (PDTC). |
| T9 |
1154-1375 |
Sentence |
denotes |
As well as culminating in the inducible phosphorylation of I kappaB alpha on serines 32 and 36, all the stimuli that are inactive on 1.3E2 cells exhibit a sensitivity to the antioxidant pyrrolidine dithiocarbamate (PDTC). |
| T10 |
1376-1531 |
Sentence |
denotes |
In contrast, stimuli such as hyperosmotic shock or phosphatase inhibitors, which use PDTC-insensitive pathways, induce I kappaB alpha degradation in 1.3E2. |
| T10 |
1376-1531 |
Sentence |
denotes |
In contrast, stimuli such as hyperosmotic shock or phosphatase inhibitors, which use PDTC-insensitive pathways, induce I kappaB alpha degradation in 1.3E2. |
| T11 |
1532-1622 |
Sentence |
denotes |
Analysis of the redox status of 1.3E2 does not reveal any difference from wild-type 70Z/3. |
| T11 |
1532-1622 |
Sentence |
denotes |
Analysis of the redox status of 1.3E2 does not reveal any difference from wild-type 70Z/3. |
| T12 |
1623-1834 |
Sentence |
denotes |
We also report that the human T-cell leukemia virus type 1 (HTLV-1)-derived Tax trans-activator induces NF-kappaB activity in 1.3E2, suggesting that this viral protein does not operate via the defective pathway. |
| T12 |
1623-1834 |
Sentence |
denotes |
We also report that the human T-cell leukemia virus type 1 (HTLV-1)-derived Tax trans-activator induces NF-kappaB activity in 1.3E2, suggesting that this viral protein does not operate via the defective pathway. |
| T13 |
1835-2009 |
Sentence |
denotes |
Finally, we show that two other I kappaB molecules, I kappaB beta and the recently identified I kappaB epsilon, are not degraded in the 1.3E2 cell line following stimulation. |
| T13 |
1835-2009 |
Sentence |
denotes |
Finally, we show that two other I kappaB molecules, I kappaB beta and the recently identified I kappaB epsilon, are not degraded in the 1.3E2 cell line following stimulation. |
| T14 |
2010-2177 |
Sentence |
denotes |
Our results demonstrate that 1.3E2 is a cellular transduction mutant exhibiting a defect in a step that is required by several different stimuli to activate NF-kappaB. |
| T14 |
2010-2177 |
Sentence |
denotes |
Our results demonstrate that 1.3E2 is a cellular transduction mutant exhibiting a defect in a step that is required by several different stimuli to activate NF-kappaB. |
| T15 |
2178-2331 |
Sentence |
denotes |
In addition, this analysis suggests a common step in the signaling pathways that trigger I kappaB alpha, I kappaB beta, and I kappaB epsilon degradation. |
| T15 |
2178-2331 |
Sentence |
denotes |
In addition, this analysis suggests a common step in the signaling pathways that trigger I kappaB alpha, I kappaB beta, and I kappaB epsilon degradation. |