Transcriptome dynamics of Deinococcus radiodurans recovering from ionizing radiation

被引:321
作者
Liu, YQ
Zhou, JZ
Omelchenko, MV
Beliaev, AS
Venkateswaran, A
Stair, J
Wu, LY
Thompson, DK
Xu, D
Rogozin, IB
Gaidamakova, EK
Zhai, M
Makarova, KS
Koonin, EV
Daly, MJ
机构
[1] Oak Ridge Natl Lab, Div Environm Sci, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Div Life Sci, Oak Ridge, TN 37831 USA
[3] Michigan State Univ, Ctr Microbial Ecol, E Lansing, MI 48824 USA
[4] NIH, Ctr Biotechnol Informat, Bethesda, MD 20894 USA
[5] Uniformed Serv Univ Hlth Sci, Bethesda, MD 20814 USA
关键词
D O I
10.1073/pnas.0630387100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Deinococcus radiodurans R1 (DEIRA) is a bacterium best known for its extreme resistance to the lethal effects of ionizing radiation, but the molecular mechanisms underlying this phenotype remain poorly understood. To define the repertoire of DEIRA genes responding to acute irradiation (15 kGy), transcriptome dynamics were examined in cells representing early, middle, and late phases of recovery by using DNA microarrays covering approximate to94% of its predicted genes. At least at one time point during DEIRA recovery, 832 genes (28% of the genome) were induced and 451 genes (15%) were repressed 2-fold or more. The expression patterns of the majority of the induced genes resemble the previously characterized expression profile of recA after irradiation. DEIRA recA, which is central to genomic restoration after irradiation, is substantially up-regulated on DNA damage (early phase) and down-regulated before the onset of exponential growth (late phase). Many other genes were expressed later in recovery, displaying a growth-related pattern of induction. Genes induced in the early phase of recovery included those involved in DNA replication, repair, and recombination, cell wall metabolism, cellular transport, and many encoding uncharacterized proteins. Collectively, the microarray data suggest that DEIRA cells efficiently coordinate their recovery by a complex network, within which both DNA repair and metabolic functions play critical roles. Components of this network include a predicted distinct ATP-dependent DNA ligase and metabolic pathway switching that could prevent additional genomic damage elicited by metabolism-induced free radicals.
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收藏
页码:4191 / 4196
页数:6
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