Automethylation of protein arginine methyltransferase 7 and its impact on breast cancer progression. Issue 6 (10th February 2017)
- Record Type:
- Journal Article
- Title:
- Automethylation of protein arginine methyltransferase 7 and its impact on breast cancer progression. Issue 6 (10th February 2017)
- Main Title:
- Automethylation of protein arginine methyltransferase 7 and its impact on breast cancer progression
- Authors:
- Geng, Pengyu
Zhang, Yu
Liu, Xiaoqing
Zhang, Na
Liu, Yingqi
Liu, Xin
Lin, Cong
Yan, Xu
Li, Zhongwei
Wang, Guannan
Li, Yuxin
Tan, Jiang
Liu, Dong‐Xu
Huang, Baiqu
Lu, Jun - Abstract:
- ABSTRACT: Protein arginine methyltransferases (PRMTs) catalyze protein arginine methylation and are linked to carcinogenesis and metastasis. Some members of PRMTs have been found to undergo automethylation; however, the biologic significance of this self‐modification is not entirely clear. In this report, we demonstrate that R531 of PRMT7 is self‐methylated, both in vitro and in vivo . Automethylation of PRMT7 plays a key role in inducing the epithelial–mesenchymal transition (EMT) program and in promoting the migratory and invasive behavior of breast cancer cells. We also prove in a nude mouse model that expression of wild‐type PRMT7 in MCF7 breast cancer cells promotes metastasis in vivo, in contrast to the PRMT7 R531K mutant (a mimic of the unmethylated status). Moreover, our immunohistochemical data unravel a close link between PRMT7 automethylation and the clinical outcome of breast carcinomas. Mechanistically, we determine that loss of PRMT7 automethylation leads to the reduction of its recruitment to the E‐cadherin promoter by YY1, which consequently derepresses the E‐cadherin expression through decreasing the H4R3me2s level. The findings in this work define a novel post‐translational modification of PRMT7 that has a promoting impact on breast cancer metastasis.—Geng, P., Zhang, Y., Liu, X., Zhang, N., Liu, Y., Liu, X., Lin, C., Yan, X., Li, Z., Wang, G., Li, Y., Tan, J., Liu, D.‐X., Huang, B., Lu, J. Automethylation of protein arginine methyltransferase 7 and itsABSTRACT: Protein arginine methyltransferases (PRMTs) catalyze protein arginine methylation and are linked to carcinogenesis and metastasis. Some members of PRMTs have been found to undergo automethylation; however, the biologic significance of this self‐modification is not entirely clear. In this report, we demonstrate that R531 of PRMT7 is self‐methylated, both in vitro and in vivo . Automethylation of PRMT7 plays a key role in inducing the epithelial–mesenchymal transition (EMT) program and in promoting the migratory and invasive behavior of breast cancer cells. We also prove in a nude mouse model that expression of wild‐type PRMT7 in MCF7 breast cancer cells promotes metastasis in vivo, in contrast to the PRMT7 R531K mutant (a mimic of the unmethylated status). Moreover, our immunohistochemical data unravel a close link between PRMT7 automethylation and the clinical outcome of breast carcinomas. Mechanistically, we determine that loss of PRMT7 automethylation leads to the reduction of its recruitment to the E‐cadherin promoter by YY1, which consequently derepresses the E‐cadherin expression through decreasing the H4R3me2s level. The findings in this work define a novel post‐translational modification of PRMT7 that has a promoting impact on breast cancer metastasis.—Geng, P., Zhang, Y., Liu, X., Zhang, N., Liu, Y., Liu, X., Lin, C., Yan, X., Li, Z., Wang, G., Li, Y., Tan, J., Liu, D.‐X., Huang, B., Lu, J. Automethylation of protein arginine methyltransferase 7 and its impact on breast cancer progression. FASEB J. 31, 2287–2300 (2017). www.fasebj.org … (more)
- Is Part Of:
- FASEB journal. Volume 31:Issue 6(2017)
- Journal:
- FASEB journal
- Issue:
- Volume 31:Issue 6(2017)
- Issue Display:
- Volume 31, Issue 6 (2017)
- Year:
- 2017
- Volume:
- 31
- Issue:
- 6
- Issue Sort Value:
- 2017-0031-0006-0000
- Page Start:
- 2287
- Page End:
- 2300
- Publication Date:
- 2017-02-10
- Subjects:
- migration -- invasion -- E‐cadherin -- YY1
Biology -- Periodicals
Biology, Experimental -- Periodicals
570 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1096/fj.201601196R ↗
- Languages:
- English
- ISSNs:
- 0892-6638
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 13308.xml