Zobrazeno 1 - 10
of 74
pro vyhledávání: '"Takayasu Date"'
Autor:
Yuri Tsuji, Takayasu Date, Kuniyoshi Iwabuchi, Kazuaki Tokunaga, Jinghua Sun, Tokio Tani, Mitsumasa Hashimoto, Masaru Yamaizumi, Satoshi Tateishi, Kenji Watanabe
Publikováno v:
Nucleic Acids Research
Recruitment of RAD18 to stalled replication forks facilitates monoubiquitination of PCNA during S-phase, promoting translesion synthesis at sites of UV irradiation-induced DNA damage. In this study, we show that RAD18 is also recruited to ionizing ra
Cell sorting analysis of cell cycle-dependent X-ray sensitivity in end joining-deficient human cells
Autor:
Kuniyoshi Iwabuchi, Tadashi Matsui, Takayasu Date, Mitsumasa Hashimoto, Noritaka Adachi, Aya Kurosawa
Publikováno v:
Biochemical and Biophysical Research Communications. 372:662-667
Non-homologous end joining (NHEJ) plays a major role in the repair of ionizing radiation-induced DNA double-strand breaks (DSBs), especially during the G1-phase of the cell cycle. Using a flow cytometric cell sorter, we fractionated G1- and S/G2-phas
Autor:
Tsukasa Matsunaga, Megumi Matsumoto, Kuniyoshi Iwabuchi, Kanji Ishizaki, Mayumi Imura, Toshio Mori, Manabu Inobe, Mizuho Hasegawa, Takayasu Date, Kie Yaginuma, Ai Igarashi, Katsumi Yamashita
Publikováno v:
Journal of Cell Science. 120:1104-1112
Human histone H2AX is rapidly phosphorylated on serine 139 in response to DNA double-strand breaks and plays a crucial role in tethering the factors involved in DNA repair and damage signaling. Replication stress caused by hydroxyurea or UV also init
Autor:
Shogo Katsuda, Tomio Hamada, Yasunori Okada, Takayasu Date, Hideaki Iizuka, Yoshimichi Ueda, Yasuo Sasagawa, Kiran Chada, Takuya Akai
Publikováno v:
Pathology - Research and Practice. 200:619-624
High mobility group I-C (HMGI-C) protein is a non-histone DNA-binding factor that organizes active chromatin. This protein is expressed during the limited phase of embryonic development and may regulate the expression of genes critical for embryonic
Publikováno v:
Biochemical and Biophysical Research Communications. 284:798-807
Interferon (IFN)-inducible, double-stranded (dsRNA)-activated protein kinase (PKR) is a key mediator of the antiviral and antiproliferative effects of IFN. PKR is present within cells in a latent state. In response to binding dsRNA, the enzyme become
Publikováno v:
The Journal of Cell Biology
The tumor suppressor p53 binding protein 1 (53BP1) binds to the DNA-binding domain of p53 and enhances p53-mediated transcriptional activation. 53BP1 contains two breast cancer susceptibility gene 1 COOH terminus (BRCT) motifs, which are present in s
Autor:
Takayasu Date, Mineo Saneyoshi, Toyofumi Yamaguchi, Fumio Sugawara, Kengo Sakaguchi, Yoshiyuki Mizushina, Tadayasu Ohkubo
Publikováno v:
Journal of Biological Chemistry. 274:25599-25607
We reported previously that long-chain fatty acids are potent inhibitors of mammalian DNA polymerase beta. At present, based on information available from the NMR structure of the N-terminal 8-kDa domain, we examined the structural interaction with t
Autor:
Kunihiko Wakaki, Mohammad R. Eskandarian, Masashi Kobayashi, Takayasu Date, Num-Ho Huh, Hirofumi Ogawa, Henry C. Pitot, Fusao Takusagawa, Hiroyuki Kishi
Publikováno v:
Journal of Biological Chemistry. 274:12855-12860
A pCW vector harboring rat liver serine dehydratase cDNA was expressed in Escherichia coli. The expressed level was about 5-fold higher in E. coli BL21 than in JM109 cell extract; the former lacked two kinds of proteases. Immunoblot analysis revealed
Publikováno v:
Journal of Biological Chemistry. 273:26061-26068
p53 is a tumor suppressor protein that controls cell proliferation by regulating the expression of growth control genes. In a previous study, we identified two proteins, 53BP1 and 53BP2, that are able to bind to wild type but not to mutant p53 via th
Autor:
Kiyomi Tanihara, Ayanori Yamakawa, Yosuke Kameoka, Katsuzo Nishikawa, Katsuyuki Hashimoto, Takayasu Date, Yoshino Yoshitake
Publikováno v:
Gene. 202:193-201
We have cloned cDNAs for novel serine/threonine protein kinases (PK), termed PKU-alpha and PKU-beta, by screening a bacteriophage expression library for kinase activity. Sequence analysis of PKU-alpha and PKU-beta genes revealed that their open readi