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Updated: Jun 12, 2026

Temporal Quantification of MAPK Induced Expression in Single Yeast Cells
Published on: October 4, 2013
[Construction of eukaryotic plasmid expression Hsf4b and phosphorylation of Hsf4b by MAP kinase P38]
Zheng-yi Ma1, Jun Zhang, Xue-li Li
1Key laboratory of Cell and Molecular Immunology, Medical college of Henan University, Kaifeng, China.
Aim:
Ton construct eukaryotic plasmid expressing Hsf4B and to investigate Hsf4b is phosphorylated by MAP kinase P38:
Methods:
The total RNA of human heart tissues were prepared. Hsf4b cDNA were then synthesized with RT-PCR. The PCR products were digested with Kpn I and EcoR I and subcloned into pcDNA3.0, pcDNA-Flag-Hsf4b was transfected into HEK293T cells. The expression of Hsf4b was testified with Western blotting. The interaction between Hsf4b and P38 was assayed by immunoprecipitation. In vivo pull down GST demonstrated that Hsf4B (196-493) could interact with P38, P38 phosphorylation of Hsf4b were testified with Kinase assay.
Results:
We subcloned the human cDNA of Hsf4b into eukaryotic expression vectors pcDNA3 and PEBG, and Hsf4b was overexpressed in HEK293T cells. Further studies demonstrated that Hsf4b could interact with and phosphorylated by MAP kinase P38.
Conclusion:
Hsf4b could interact with and phosphorylated by MAP kinase P38. Our results will provide more evidence for understanding the signal regulation of Hsf4b transcription activity during lens development.
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