Effects of AML1-ETO on transcription activity of p21WAF1/CIP1 gene promoter / 中华血液学杂志
Chinese Journal of Hematology
; (12): 545-548, 2007.
Article
in Zh
| WPRIM
| ID: wpr-262986
Responsible library:
WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To observe the effects of AML1-ETO fusion gene on the transcription activity of p21WAF1/CIP1 gene. And to explore the enhancement of leukemia pathogenesis of AML1-ETO.</p><p><b>METHODS</b>The luciferase reporter plasmids of p21WAF1/CIP1 gene promoter were constructed, and co-transfected into CV-1 cells with AML1-ETO, AML1b and AML1a expression plasmids. The trans-activity of p21WAF1/CIP1 gene promoter was assayed by luminometer.</p><p><b>RESULTS</b>AML1-ETO exhibited a distinct inhibition activity of p21WAF1/CIP1 gene promoter with a sequence-specificity and dosage-dependent manner. The trans-activity of p21WAF1/CIP1 gene promoter decreased to (19 +/- 4)% compared to control group, when 1000 ng pCMV5-AML1-ETO plasmid was used. AML1b and AMLla showed less inhibition activity. The trans-activity of p21WAF1/CIP1 gene promoter decreased to (61 +/- 16)% and (59 +/- 16)% compared to control group, respectively, when 1000 ng plasmid was used.</p><p><b>CONCLUSION</b>AML1-ETO exhibits more inhibition activity of p21WAF1/CIP1 gene promoter than AML1b and AMLla, results from recruiting transcription co-repression complex efficiently by ETO. Based on previous researches, the effects of exogenous AML1-ETO on p21WAF1/CIP1 gene promote may be dependent on the type of cell lines.</p>
Full text:
1
Index:
WPRIM
Main subject:
Plasmids
/
Transcription, Genetic
/
Transfection
/
Oncogene Proteins, Fusion
/
Cell Line
/
Promoter Regions, Genetic
/
Haplorhini
/
Cyclin-Dependent Kinase Inhibitor p21
/
Core Binding Factor Alpha 2 Subunit
/
RUNX1 Translocation Partner 1 Protein
Limits:
Animals
Language:
Zh
Journal:
Chinese Journal of Hematology
Year:
2007
Type:
Article