Perturbation of the activity of replication origin by meiosis-specific transcription

被引:32
作者
Mori, Saori
Shirahige, Katsuhiko
机构
[1] Yokohama City Univ, Grad Sch Integrated Sci, Tsurumi Ku, Kanagawa 2300045, Japan
[2] Tokyo Inst Technol, Ctr Biol Resources & Informat, Div Gene Res, Lab Genome Struct & Funct, Kanagawa 2268501, Japan
关键词
D O I
10.1074/jbc.M609671200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have determined the activity of all ARSs on the Saccharomyces cerevisiae chromosome VI as chromosomal replication origins in premeiotic S-phase by neutral/neutral two-dimensional gel electrophoresis. The comparison of origin activity of each origin in mitotic and premeiotic S-phase showed that one of the most efficient origins in mitotic S-phase, ARS605, was completely inhibited in premeiotic S-phase. ARS605 is located within the open reading frame of MSH4 gene that is transcribed specifically during an early stage of meiosis. Systematic analysis of relationships between MSH4 transcription and ARS605 origin activity revealed that transcription of MSH4 inhibited the ARS605 origin activity by removing origin recognition complex from ARS605. Deletion of UME6, a transcription factor responsible for repressing MSH4 during mitotic S-phase, resulted in inactivation of ARS605 in mitosis. Our finding is the first demonstration that the transcriptional regulation on the replication origin activity is related to changes in cell physiology. These results may provide insights into changes in replication origin activity in embryonic cell cycle during early developmental stages.
引用
收藏
页码:4447 / 4452
页数:6
相关论文
共 34 条
[21]   Regulation of premeiotic S phase and recombination-related double-strand DNA breaks during meiosis in fission yeast [J].
Murakami, H ;
Nurse, P .
NATURE GENETICS, 2001, 28 (03) :290-293
[22]   EUKARYOTIC RNA-POLYMERASE CONDITIONAL MUTANT THAT RAPIDLY CEASES MESSENGER-RNA SYNTHESIS [J].
NONET, M ;
SCAFE, C ;
SEXTON, J ;
YOUNG, R .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (05) :1602-1611
[23]   The role and regulation of the preRC component Cdc6 in the initiation of premeiotic DNA replication [J].
Ofir, Y ;
Sagee, S ;
Guttmann-Raviv, N ;
Pnueli, L ;
Kassir, Y .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (05) :2230-2242
[24]   Mutations in the MRE11, RAD50, XRS2, and MRE2 genes alter chromatin configuration at meiotic DNA double-stranded break sites in premeiotic and meiotic cells [J].
Ohta, K ;
Nicolas, A ;
Furuse, M ;
Nabetani, A ;
Ogawa, H ;
Shibata, T .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (02) :646-651
[25]   Replication dynamics of the yeast genome [J].
Raghuraman, MK ;
Winzeler, EA ;
Collingwood, D ;
Hunt, S ;
Wodicka, L ;
Conway, A ;
Lockhart, DJ ;
Davis, RW ;
Brewer, BJ ;
Fangman, WL .
SCIENCE, 2001, 294 (5540) :115-121
[26]   MUTATION OF A MEIOSIS-SPECIFIC MUTS HOMOLOG DECREASES CROSSING-OVER BUT NOT MISMATCH CORRECTION [J].
ROSSMACDONALD, P ;
ROEDER, GS .
CELL, 1994, 79 (06) :1069-1080
[27]   A Mec1- and Rad53-dependent checkpoint controls late-firing origins of DNA replication [J].
Santocanale, C ;
Diffley, JFX .
NATURE, 1998, 395 (6702) :615-618
[28]   Regulation of DNA-replication origins during cell-cycle progression [J].
Shirahige, K ;
Hori, Y ;
Shiraishi, K ;
Yamashita, M ;
Takahashi, K ;
Obuse, C ;
Tsurimoto, T ;
Yoshikawa, H .
NATURE, 1998, 395 (6702) :618-621
[29]   LOCATION AND CHARACTERIZATION OF AUTONOMOUSLY REPLICATING SEQUENCES FROM CHROMOSOME-VI OF SACCHAROMYCES-CEREVISIAE [J].
SHIRAHIGE, K ;
IWASAKI, T ;
RASHID, MB ;
OGASAWARA, N ;
YOSHIKAWA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (08) :5043-5056
[30]   TRANSCRIPTION INTERFERES WITH ELEMENTS IMPORTANT FOR CHROMOSOME MAINTENANCE IN SACCHAROMYCES-CEREVISIAE [J].
SNYDER, M ;
SAPOLSKY, RJ ;
DAVIS, RW .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (05) :2184-2194