Autorepression of Rfx1 gene expression: Functional conservation from yeast to humans in response to DNA replication arrest

被引:40
作者
Lubelsky, Y [1 ]
Reuven, N [1 ]
Shaul, Y [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
关键词
D O I
10.1128/MCB.25.23.10665-10673.2005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
The yeast Saccharomyces cerevisiae Crt1 transcription repressor is an effector of the DNA damage and replication checkpoint pathway. Crt1 binds and represses genes encoding ribonucleotide reductase (RNR) and its own promoter, establishing a negative-feedback pathway. The role of Rfx1, the mammalian Crt1 homologue, remained uncertain. In this study we investigated the possibility that Rfx1 plays a similar function in animal cells. We show here that, like Crt1, Rfx1 binds and represses its own promoter. Furthermore, Rfx1 binding to its promoter is reduced upon induction of a DNA replication block by hydroxyurea, which led to a release of repression. Significantly, like Crt1, Rfx1 binds and represses the RNR-R2 gene. Upon blocking replication and UV treatment, expression of both Rfx1 and RNR-R2 is induced; however, unlike the results seen with the RNR-R2 gene, the derepression of the RFX1 gene is only partially blocked by inhibiting Chk1, the DNA checkpoint kinase. This report provides evidence for a common mechanism for Crt1 and Rfx1 expression and for the conservation of their mode of action in response to a DNA replication block. We suggest that Rfx1 plays a role in the DNA damage response by down-regulating a subset of genes whose expression is increased in response to replication blocking and UV-induced DNA damage.
引用
收藏
页码:10665 / 10673
页数:9
相关论文
共 49 条
[1]
Cell cycle checkpoint signaling through the ATM and ATR kinases [J].
Abraham, RT .
GENES & DEVELOPMENT, 2001, 15 (17) :2177-2196
[3]
Mechanism of rapid transcriptional induction of tumor necrosis factor alpha-responsive genes by NF-κB [J].
Ainbinder, E ;
Revach, M ;
Wolstein, O ;
Moshonov, S ;
Diamant, N ;
Dikstein, R .
MOLECULAR AND CELLULAR BIOLOGY, 2002, 22 (18) :6354-6362
[4]
Restricted expression and photic induction of a novel mouse regulatory factor X4 transcript in the suprachiasmatic nucleus [J].
Araki, R ;
Takahashi, H ;
Fukumura, R ;
Sun, FY ;
Umeda, N ;
Sujino, M ;
Inouye, SIT ;
Saito, T ;
Abe, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (11) :10237-10242
[5]
Graded phenotypic response to partial and complete deficiency of a brain-specific transcript variant of the winged helix transcription factor RFX4 [J].
Blackshear, PJ ;
Graves, JP ;
Stumpo, DJ ;
Cobos, I ;
Rubenstein, JLR ;
Zeldin, DC .
DEVELOPMENT, 2003, 130 (19) :4539-4552
[6]
The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specification [J].
Bonnafe, E ;
Touka, M ;
AitLounis, A ;
Baas, D ;
Barras, E ;
Ucla, C ;
Moreau, A ;
Flamant, F ;
Dubruille, R ;
Couble, P ;
Collignon, J ;
Durand, B ;
Reith, W .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (10) :4417-4427
[7]
Stable suppression of tumorigenicity by virus-mediated RNA interference [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
CANCER CELL, 2002, 2 (03) :243-247
[8]
A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[9]
Activation of protein kinase C induces nuclear translocation of RFX1 and down-regulates c-myc via an intron 1 X box in undifferentiated leukemia HL-60 cells [J].
Chen, L ;
Smith, L ;
Johnson, MR ;
Wang, KS ;
Diasio, RB ;
Smith, JB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :32227-32233
[10]
INTERACTION OF EF-C/RFX-1 WITH THE INVERTED REPEAT OF VIRAL ENHANCE REGIONS IS REQUIRED FOR TRANSACTIVATION [J].
DAVID, E ;
GARCIA, AD ;
HEARING, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (14) :8353-8360