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JCR 2016
جستجوی مقالات
یکشنبه 23 آذر 1404
Iranian Biomedical Journal
، جلد ۲۷، شماره ۴، صفحات ۱۸۳-۱۹۰
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Gαq Signaling Activates β-Catenin-Dependent Gene Transcription
چکیده انگلیسی مقاله
Background
: The canonical Wnt signal transduction or the Wnt/
β
-catenin pathway plays a crucial role in both carcinogenesis and development of animals. Activation of the G
α
q class of G
α
proteins positively regulates Wnt/
β
-catenin pathway, and expression of G
α
q in
human embryonic kidney 293 (
HEK293T) cells or
Xenopus
oocytes leads to the inhibition of
glycogen synthase kinase-3 beta
and cellular accumulation of
β
-catenin. This study investigated whether G
α
q-mediated cellular accumulation of
β-catenin could affect the transcriptional activity of this protein.
Methods:
HEK-293T and HT-29 cells were used for cell culture and transfection. Protein localization and quantification were assessed by using immunofluorescence microscopy, cell fractionation assay, and Western blotting analysis. Gene expression at the transcription level was examined by quantitative reverse
transcriptase/real-time PCR method.
Results
: Transcription of two cellular
β
-catenin target genes (
c-MYC
and
CCND1
) and the
β
-catenin/
T-cell factor
reporter
luciferase
gene (TopFlash plasmid) significantly increased by G
α
q activation. The G
α
q-mediated increase in the expression level of the
β
-catenin-target genes was sensitive to the expression of a minigene encoding a specific G
α
q blocking peptide. The results of cell fractionation and Western blotting experiments showed that activation of G
α
q signaling increased the intracellular
β-catenin protein level, but it blocked its membrane localization.
Conclusion
:
Our results reveal that the G
α
q-dependent cellular accumulation of
β
-catenin can enhance
β
-catenin transcriptional activity.
کلیدواژههای انگلیسی مقاله
β-catenin, Wnt signaling, G proteins
نویسندگان مقاله
| Sara Ansari
Department of Cell and Molecular Biology, School of Biology, College of Sciences, University of Tehran, P.O.Box 14155-6455, Tehran, Iran
| Sedighe Kolivand
Department of Cell and Molecular Biology, School of Biology, College of Sciences, University of Tehran, P.O.Box 14155-6455, Tehran, Iran
| Sara Salmanian
Department of Cell and Molecular Biology, School of Biology, College of Sciences, University of Tehran, P.O.Box 14155-6455, Tehran, Iran
| Marie Saghaeian Jazi
Department of Cell and Molecular Biology, School of Biology, College of Sciences, University of Tehran, P.O.Box 14155-6455, Tehran, Iran
| S Mahmoud A Najafi
Department of Cell and Molecular Biology, School of Biology, College of Sciences, University of Tehran, P.O.Box 14155-6455, Tehran, Iran
نشانی اینترنتی
http://ibj.pasteur.ac.ir/browse.php?a_code=A-10-3459-3&slc_lang=en&sid=1
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کد مقاله (doi)
زبان مقاله منتشر شده
en
موضوعات مقاله منتشر شده
Cancer Biology
نوع مقاله منتشر شده
مقاله کامل
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