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Takahashi, Akihisa*; Kubo, Makoto*; Ma, H.*; Nakagawa, Akiko*; Yoshida, Yukari*; Isono, Mayu*; Kanai, Tatsuaki*; Ono, Tatsuya*; Furusawa, Yoshiya*; Funayama, Tomoo; et al.
Radiation Research, 182(3), p.338 - 344, 2014/09
Times Cited Count:60 Percentile:89.83(Biology)To clarify whether high-LET radiation inhibits all repair pathways or specifically one repair pathway, studies were designed to examine the effects of radiation with different LET values on DNA DSB repair and radiosensitivity. Embryonic fibroblasts bearing repair gene KO were exposed to X rays, carbon-, iron-, neon- and argon-ion beams. Cell survival was measured with colony-forming assays. The sensitization enhancement ratio (SER) values were calculated using the 10% survival dose of wild-type cells and repair-deficient cells. Cellular radiosensitivity was listed in descending order: double-KO cells NHEJ-KO cells
HR-KO cells
wild-type cells. Although HR-KO cells had an almost constant SER value, NHEJ-KO cells showed a high-SER value when compared to HR-KO cells, even with increasing LET values. These results suggest that with carbon-ion therapy, targeting NHEJ repair yields higher radiosensitivity than targeting homologous recombination repair.
Nakagawa, Mayu*; Takahashi, Shinya*; Narumi, Issei; Sakamoto, Ayako
Plant Signaling & Behavior (Internet), 6(5), p.728 - 731, 2011/05
Nefissi, R.*; Natsui, Yu*; Miyata, Kana*; Oda, Atsushi*; Hase, Yoshihiro; Nakagawa, Mayu*; Ghorbel, A.*; Mizoguchi, Tsuyoshi*
Journal of Experimental Botany, 62(8), p.2731 - 2744, 2011/02
Times Cited Count:19 Percentile:48.82(Plant Sciences)no abstracts in English
Nakagawa, Mayu*; Takahashi, Shinya*; Tanaka, Atsushi; Narumi, Issei; Sakamoto, Ayako
Plant Physiology, 155(1), p.414 - 420, 2011/01
Times Cited Count:15 Percentile:41.29(Plant Sciences)no abstracts in English
Natsui, Yu*; Nefissi, R.*; Miyata, Kana*; Oda, Atsushi*; Hase, Yoshihiro; Nakagawa, Mayu*; Mizoguchi, Tsuyoshi*
Plant Biotechnology, 27(5), p.463 - 468, 2010/12
Times Cited Count:4 Percentile:14.85(Biotechnology & Applied Microbiology)EARLY FLOWERING 3 (ELF3) is a circadian clock protein with a major role in maintaining circadian rhythms in plants. In this work, was mutagenized by EMS in plants of the Lansberg
background to isolate suppressors of
and to understand the molecular mechanisms of flowering time controlled by ELF3. Two suppressors,
obtained from this screen and
from a precious study, were chosen for further analysis. Genetic mapping, gene expression analysis, and sequencing identified
and
as new alleles of
and
, respectively. Genetic interactions between
and
and between
and
in the control of the floral activator
were also investigated. Six suppressor of
were classified at least into four subgroups based on the expression of such floral regulators as GI, CO, FT, SVP, and FLC, and on their flowering times under LL, LD, and SD. This classification scheme is useful for the characterization of unidentified suppressor mutations.
Sakamoto, Ayako; Lan, V. T. T.*; Puripunyavanich, V.*; Hase, Yoshihiro; Yokota, Yuichiro; Shikazono, Naoya; Nakagawa, Mayu*; Narumi, Issei; Tanaka, Atsushi
Plant Journal, 60(3), p.509 - 517, 2009/07
Times Cited Count:21 Percentile:48.48(Plant Sciences)no abstracts in English
Takahashi, Shinya*; Nakagawa, Mayu; Tanaka, Atsushi; Narumi, Issei; Shimizu, Kikuo*; Sakamoto, Ayako
JAEA-Review 2008-055, JAEA Takasaki Annual Report 2007, P. 58, 2008/11
no abstracts in English
Nefissi, R.*; Miyata, Kana*; Niinuma, Kanae*; Oda, Atsushi*; Hase, Yoshihiro; Nakagawa, Mayu; Mizoguchi, Tsuyoshi*
JAEA-Review 2008-055, JAEA Takasaki Annual Report 2007, P. 77, 2008/11
no abstracts in English
Anderson, H.*; Vonarx, E.*; Pastushok, L.*; Nakagawa, Mayu; Katafuchi, Atsushi*; Gruz, P.*; Rubbo, A.*; Grice, D.*; Osmond, M.*; Sakamoto, Ayako; et al.
Plant Journal, 55(6), p.895 - 908, 2008/09
Times Cited Count:43 Percentile:71.66(Plant Sciences)Oda, Atsushi*; Reeves, P. H.*; Tajima, Takeomi*; Nakagawa, Mayu; Kamada, Hiroshi*; Coupland, G.*; Mizoguchi, Tsuyoshi*
Plant Biotechnology, 24(5), p.457 - 465, 2007/12
Times Cited Count:2 Percentile:7.25(Biotechnology & Applied Microbiology)no abstracts in English
Tajima, Takeomi*; Oda, Atsushi*; Nakagawa, Mayu; Kamada, Hiroshi*; Mizoguchi, Tsuyoshi*
Plant Biotechnology, 24(2), p.237 - 240, 2007/03
Times Cited Count:23 Percentile:47.88(Biotechnology & Applied Microbiology)no abstracts in English
Niinuma, Kanae*; Nakagawa, Mayu; Calvino, M.*; Mizoguchi, Tsuyoshi*
Plant Biotechnology, 24(1), p.87 - 97, 2007/03
Times Cited Count:14 Percentile:15.61(Biotechnology & Applied Microbiology)no abstracts in English
Nakagawa, Mayu; Sakamoto, Ayako; Takahashi, Shinya*; Tanaka, Atsushi; Narumi, Issei
no journal, ,
no abstracts in English
Nakagawa, Mayu; Sakamoto, Ayako; Takahashi, Shinya*; Tanaka, Atsushi; Narumi, Issei
no journal, ,
Plants were exposed to the various DNA-damaging stress in daily life. To survive in such hostile environments, plants developed many mechanisms to avoid or to repair the DNA damage. Yeast and mammals have a mechanism named translesion syntheses (TLS), in which DNA damage is bypassed by specific DNA polymerases. However, TLS generates mutations as a result of incorrect replication (error-prone TLS). We have previously isolated AtREV3, AtREV1 and AtREV7 genes, which are homolog of yeast TLS polymerases. We also showed that disruption of these genes made the plants sensitive to UV-B, -ray and MMC. To determine whether AtREV3 acts in the error-prone TLS, we utilized the beta-glucuronidase (uidA) gene containing single nonsense mutations. Transgenic plants with inactivated uidA were treated with UV-C and reversion events were counted. As a result, mutation frequency was reduced in the rev3 background, indicating that AtREV3 acts in the error-prone TLS in Arabidopsis.
Nakagawa, Mayu; Takahashi, Shinya*; Sakamoto, Ayako; Tanaka, Atsushi; Narumi, Issei
no journal, ,
no abstracts in English
Nakagawa, Mayu; Sakamoto, Ayako; Takahashi, Shinya*; Tanaka, Atsushi; Narumi, Issei
no journal, ,
no abstracts in English
Natsui, Yu*; Nefissi, R.*; Miyata, Kana*; Oda, Atsushi*; Hase, Yoshihiro; Nakagawa, Mayu; Mizoguchi, Tsuyoshi*
no journal, ,
EARLY FLOWERING 3 (ELF3) plays key roles in the control of light response, organ elongation, flowering time and circadian rhythms in Arabidopsis. ELF3 does not show significant homology to any other proteins in the public databases. Therefore biochemical function of the ELF3 has not been well understood. To understand molecular mechanisms underlying the a variety of phenotypes in the elf3 mutants, suppressors of elf3-1 were screened for, using the elf3-1 seeds mutagenized with heavy ion beams. Here we demonstrate that in one of the suppressor lines, S#20, early flowering, small cotyledon and pale green phenotypes of elf3-1 were suppressed, whereas long hypocotyl phenotype was enhanced. The recessive suppressor mutation was named suppressor of elf3 20 (sel20) and mapped to the upper side of Ch1. We have found 21-bp deletion in the FHA/CRY2 gene in the sel20. We will discuss possible roles of CRY2 in the multiple functions of ELF3.
Sakamoto, Ayako; Nakagawa, Mayu; Narumi, Issei
no journal, ,
no abstracts in English
Sakamoto, Ayako; Nakagawa, Mayu; Sato, Katsuya; Narumi, Issei
no journal, ,
no abstracts in English
Nakagawa, Mayu*; Sakamoto, Ayako; Takahashi, Shinya*; Tanaka, Atsushi; Narumi, Issei
no journal, ,
Translesion synthesis (TLS) is a damage tolerance mechanism in which the unrepaired DNA damage is bypassed by the action of specific polymerases. We have previously isolated ,
and
genes, which are homolog of yeast TLS polymerases. Disruption of any of
,
or
made the plants more sensitive to UV than the wild type. To analyze the functions of
,
and
, we further analyzed the UV-induced mutation frequency in
,
and
. As a result, the UV-induced reversion frequencies were significantly lower in
and
mutants than that in wild-type, while
mutants exhibited significantly increased reversion frequency. These results suggest that r
,
and
genes play an important role in the UV-induced mutation mechanism.