Id |
Subject |
Object |
Predicate |
Lexical cue |
T1 |
0-106 |
Sentence |
denotes |
Cross-talk between different enhancer elements during mitogenic induction of the human stromelysin-1 gene. |
T2 |
107-261 |
Sentence |
denotes |
Platelet-derived growth factor (PDGF) induces the expression of human stromelysin-1, a matrix metalloproteinase involved in tumor invasion and metastasis. |
T3 |
262-577 |
Sentence |
denotes |
Here it is shown that stromelysin-1 gene induction by PDGF depends on Ras and involves three previously identified promoter elements (the stromelysin-1 PDGF-responsive element (SPRE) site, the two head-to-head polyomavirus enhancer A-binding protein-3 (PEA3) sites, and the activator protein-1 (AP-1) binding site). |
T4 |
578-771 |
Sentence |
denotes |
During mitogenic induction, these responsive elements appear to be organized in two independent transcriptional units, SPRE-AP-1 and PEA3-AP-1, which result from specific element cross-talking. |
T5 |
772-945 |
Sentence |
denotes |
Interestingly, expression of a dominant negative mutant of Raf-1 significantly interfered with the induction through PEA3-AP-1 but not with that operating through SPRE-AP-1. |
T6 |
946-1142 |
Sentence |
denotes |
Conversely, only the induction operating through SPRE-AP-1 was affected significantly by the expression of a dominant negative mutant of the atypical lambda/iota protein kinase C (lambda/iotaPKC). |
T7 |
1143-1400 |
Sentence |
denotes |
These data strongly suggest that the signal triggered by PDGF flows through Ras and bifurcates toward two distinct pathways, one operating through Raf and involving PEA3-AP-1 and the other one Raf-independent, operating through lambda/iotaPKC and SPRE-AP-1. |
T8 |
1401-1555 |
Sentence |
denotes |
Furthermore, we present evidence suggesting that the novel SPRE-binding transcription factor SPBP cross-couples with c-Jun to transactivate the SPRE site. |
T1 |
0-106 |
Sentence |
denotes |
Cross-talk between different enhancer elements during mitogenic induction of the human stromelysin-1 gene. |
T2 |
107-261 |
Sentence |
denotes |
Platelet-derived growth factor (PDGF) induces the expression of human stromelysin-1, a matrix metalloproteinase involved in tumor invasion and metastasis. |
T3 |
262-577 |
Sentence |
denotes |
Here it is shown that stromelysin-1 gene induction by PDGF depends on Ras and involves three previously identified promoter elements (the stromelysin-1 PDGF-responsive element (SPRE) site, the two head-to-head polyomavirus enhancer A-binding protein-3 (PEA3) sites, and the activator protein-1 (AP-1) binding site). |
T4 |
578-771 |
Sentence |
denotes |
During mitogenic induction, these responsive elements appear to be organized in two independent transcriptional units, SPRE-AP-1 and PEA3-AP-1, which result from specific element cross-talking. |
T5 |
772-945 |
Sentence |
denotes |
Interestingly, expression of a dominant negative mutant of Raf-1 significantly interfered with the induction through PEA3-AP-1 but not with that operating through SPRE-AP-1. |
T6 |
946-1142 |
Sentence |
denotes |
Conversely, only the induction operating through SPRE-AP-1 was affected significantly by the expression of a dominant negative mutant of the atypical lambda/iota protein kinase C (lambda/iotaPKC). |
T7 |
1143-1400 |
Sentence |
denotes |
These data strongly suggest that the signal triggered by PDGF flows through Ras and bifurcates toward two distinct pathways, one operating through Raf and involving PEA3-AP-1 and the other one Raf-independent, operating through lambda/iotaPKC and SPRE-AP-1. |
T8 |
1401-1555 |
Sentence |
denotes |
Furthermore, we present evidence suggesting that the novel SPRE-binding transcription factor SPBP cross-couples with c-Jun to transactivate the SPRE site. |