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- Igarashi, KazuhikoRemove Igarashi, Kazuhiko filter
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Author
- Motohashi, Hozumi2
- Muto, Akihiko2
- Nio, Masaki2
- Ochiai, Kyoko2
- Sax, Nicolas2
- Alam, Mahabub1
- Alam, Md Morshedul1
- Ando, Ryo1
- Brydun, Andrey1
- Hashimoto, Satoshi1
- Hoshikawa, Yutaka1
- Ikura, Tsuyoshi1
- Inada, Toshifumi1
- Ishii, Yusho1
- Kaneko, Mika K1
- Kato, Hiroki1
- Kato, Yukinari1
- Katoh, Yasutake1
- Kitamura, Hiroshi1
- Liu, Liang1
- Long, Nguyen Chi1
- Maeda, Tatsuya1
- Masai, Hisao1
Keyword
- gene regulation2
- methylation2
- transcription factor2
- 4E binding protein1
- 4E-BP1
- ACN1
- B cells1
- CBB1
- CHX1
- Coomassie Brilliant Blue1
- DMEM1
- Dulbecco's Modified Eagle's Medium1
- FB-MAT2A1
- FBS1
- FLAG-Bio-tagged MAT2A1
- IP1
- ITSs1
- MAT1
- Nuclear factor 2 (erythroid-derived 2-like factor) (NFE2L2) (Nrf2)1
- S-adenosylmethionine1
- S6 kinase1
- S6K1
- SAM1
- SILAC1
- TE1
Gene Regulation
4 Results
- Research ArticleOpen Access
mTORC1-independent translation control in mammalian cells by methionine adenosyltransferase 2A and S-adenosylmethionine
Journal of Biological ChemistryVol. 298Issue 7102084Published online: May 26, 2022- Mahabub Alam
- Hiroki Shima
- Yoshitaka Matsuo
- Nguyen Chi Long
- Mitsuyo Matsumoto
- Yusho Ishii
- and others
Cited in Scopus: 0Methionine adenosyltransferase (MAT) catalyzes the synthesis of S-adenosylmethionine (SAM). As the sole methyl-donor for methylation of DNA, RNA, and proteins, SAM levels affect gene expression by changing methylation patterns. Expression of MAT2A, the catalytic subunit of isozyme MAT2, is positively correlated with proliferation of cancer cells; however, how MAT2A promotes cell proliferation is largely unknown. Given that the protein synthesis is induced in proliferating cells and that RNA and protein components of translation machinery are methylated, we tested here whether MAT2 and SAM are coupled with protein synthesis. - Gene RegulationOpen Access
Glucocorticoid receptor signaling represses the antioxidant response by inhibiting histone acetylation mediated by the transcriptional activator NRF2
Journal of Biological ChemistryVol. 292Issue 18p7519–7530Published online: March 17, 2017- Md. Morshedul Alam
- Keito Okazaki
- Linh Thi Thao Nguyen
- Nao Ota
- Hiroshi Kitamura
- Shohei Murakami
- and others
Cited in Scopus: 64NRF2 (nuclear factor erythroid 2-related factor 2) is a key transcriptional activator that mediates the inducible expression of antioxidant genes. NRF2 is normally ubiquitinated by KEAP1 (Kelch-like ECH-associated protein 1) and subsequently degraded by proteasomes. Inactivation of KEAP1 by oxidative stress or electrophilic chemicals allows NRF2 to activate transcription through binding to antioxidant response elements (AREs) and recruiting histone acetyltransferase CBP (CREB-binding protein). Whereas KEAP1-dependent regulation is a major determinant of NRF2 activity, NRF2-mediated transcriptional activation varies from context to context, suggesting that other intracellular signaling cascades may impact NRF2 function. - Gene RegulationOpen Access
Epigenetic Regulation of the Blimp-1 Gene (Prdm1) in B Cells Involves Bach2 and Histone Deacetylase 3
Journal of Biological ChemistryVol. 291Issue 12p6316–6330Published online: January 19, 2016- Hiromu Tanaka
- Akihiko Muto
- Hiroki Shima
- Yasutake Katoh
- Nicolas Sax
- Shinya Tajima
- and others
Cited in Scopus: 45B lymphocyte-induced maturation protein 1 (Blimp-1) encoded by Prdm1 is a master regulator of plasma cell differentiation. The transcription factor Bach2 represses Blimp-1 expression in B cells to stall terminal differentiation, by which it supports reactions such as class switch recombination of the antibody genes. We found that histones H3 and H4 around the Prdm1 intron 5 Maf recognition element were acetylated at higher levels in X63/0 plasma cells expressing Blimp-1 than in BAL17 mature B cells lacking its expression. - Signal TransductionOpen Access
The Transcription Factor Bach2 Is Phosphorylated at Multiple Sites in Murine B Cells but a Single Site Prevents Its Nuclear Localization
Journal of Biological ChemistryVol. 291Issue 4p1826–1840Published online: November 30, 2015- Ryo Ando
- Hiroki Shima
- Toru Tamahara
- Yoshihiro Sato
- Miki Watanabe-Matsui
- Hiroki Kato
- and others
Cited in Scopus: 27The transcription factor Bach2 regulates the immune system at multiple points, including class switch recombination (CSR) in activated B cells and the function of T cells in part by restricting their terminal differentiation. However, the regulation of Bach2 expression and its activity in the immune cells are still unclear. Here, we demonstrated that Bach2 mRNA expression decreased in Pten-deficient primary B cells. Bach2 was phosphorylated in primary B cells, which was increased upon the activation of the B cell receptor by an anti-immunoglobulin M (IgM) antibody or CD40 ligand.