The Histone Chaperone Facilitates Chromatin Transcription (FACT) Protein Maintains Normal Replication Fork Rates

被引:62
作者
Abe, Takuya [2 ]
Sugimura, Kazuto [3 ,4 ]
Hosono, Yoshifumi [2 ]
Takami, Yasunari [5 ]
Akita, Motomu [2 ]
Yoshimura, Akari [2 ,6 ]
Tada, Shusuke [2 ]
Nakayama, Tatsuo [5 ]
Murofushi, Hiromu [7 ]
Okumura, Katsuzumi [3 ]
Takeda, Shunichi [8 ]
Horikoshi, Masami [1 ]
Seki, Masayuki [2 ]
Enomoto, Takemi [2 ,6 ]
机构
[1] Univ Tokyo, Inst Mol & Cellular Biosci, Dev Biol Lab, Tokyo 1110032, Japan
[2] Tohoku Univ, Grad Sch Pharmaceut Sci, Mol Cell Biol Lab, Sendai, Miyagi 9808578, Japan
[3] Mie Univ, Grad Sch Bioresources, Dept Life Sci, Tsu, Mie 5148507, Japan
[4] Mie Univ, Grad Sch Med, Dept Biochem & Prote, Tsu, Mie 5148507, Japan
[5] Miyazaki Univ, Sect Biochem & Mol Biol, Miyazaki Med Coll, Dept Med Sci, Miyazaki 8891692, Japan
[6] Musashino Univ, Fac Pharm, Pharmaceut Sci Res Inst, Tokyo 2028585, Japan
[7] Yamaguchi Univ, Grad Sch Med, Dept Appl Mol Biosci, Yamaguchi 7538512, Japan
[8] Kyoto Univ, Fac Med, Dept Radiat Genet, Kyoto 6068501, Japan
关键词
N-TERMINAL DOMAIN; DNA-REPLICATION; S-PHASE; FUNCTIONAL COOPERATION; DORMANT ORIGINS; EXCESS MCM2-7; HUMAN-CELLS; SPT16; PROGRESSION; ELONGATION;
D O I
10.1074/jbc.M111.264721
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
Ordered nucleosome disassembly and reassembly are required for eukaryotic DNA replication. The facilitates chromatin transcription (FACT) complex, a histone chaperone comprising Spt16 and SSRP1, is involved in DNA replication as well as transcription. FACT associates with the MCM helicase, which is involved in DNA replication initiation and elongation. Although the FACT-MCM complex is reported to regulate DNA replication initiation, its functional role in DNA replication elongation remains elusive. To elucidate the functional role of FACT in replication fork progression during DNA elongation in the cells, we generated and analyzed conditional SSRP1 gene knock-out chicken (Gallus gallus) DT40 cells. SSRP1-depleted cells ceased to grow and exhibited a delay in S-phase cell cycle progression, although SSRP1 depletion did not affect the level of chromatin-bound DNA polymerase alpha or nucleosome reassembly on daughter strands. The tracking length of newly synthesized-DNA, but not origin firing, was reduced in SSRP1-depleted cells, suggesting that the S-phase cell cycle delay is mainly due to the inhibition of replication fork progression rather than to defects in the initiation of DNA replication in these cells. We discuss the mechanisms of how FACT promotes replication fork progression in the cells.
引用
收藏
页码:30504 / 30512
页数:9
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