Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/98611
Title: AT-hook DNA-binding motif-containing protein one knockdown downregulates EWS - FLI1 transcriptional activity in Ewing’s sarcoma cells
Authors: Kitagawa, Takao
Kobayashi, Daiki
Baron, Byron
Okita, Hajime
Miyamoto, Tatsuo
Takai, Rie
Paudel, Durga
Ohta, Tohru
Asaoka, Yoichi
Tokunaga, Masayuki
Nakagawa, Koji
Furutani-Seiki, Makoto
Araki, Norie
Kuramitsu, Yasuhiro
Kobayashi, Masanobu
Keywords: Tumors in children
Ewing's sarcoma
Cancer in children
Transcription factors
Issue Date: 2022
Publisher: bioRxiv
Citation: Kitagawa, T., Kobayashi, D., Baron, B., Okita, H., Miyamoto, T., Takai, R., ... & Kobayashi, M. (2022). AT-hook DNA-binding motif-containing protein one knockdown downregulates EWS-FLI1 transcriptional activity in Ewing’s sarcoma cells. bioRxiv.
Abstract: Ewing’s sarcoma is the second most common bone malignancy in children or young adults and is caused by an oncogenic transcription factor by a chromosomal translocation between the EWSR1 gene and the ETS transcription factor family. However, the transcriptional mechanism of EWS-ETS fusion proteins is still unclear. To identify the transcriptional complexes of EWS-ETS fusion transcription factors, we applied a proximal labeling system called BioID in Ewing’s sarcoma cells. We identified AHDC1 as a proximal protein of EWS-ETS fusion proteins. AHDC1 knockdown showed a reduced cell growth and transcriptional activity of EWS-FLI1. AHDC1 knockdown also reduced BRD4 and BRG1 protein levels, both known as interacting proteins of EWS-FLI1. In addition, AHDC1 co-localized with BRD4. Our results suggest that AHDC1 supports cell growth through EWS-FLI1.
URI: https://www.um.edu.mt/library/oar/handle/123456789/98611
Appears in Collections:Scholarly Works - CenMMB



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