Identification and functional characterization of a new member of the human Mcm protein family:: hMcm8

被引:81
作者
Gozuacik, D
Chami, M
Lagorce, D
Faivre, J
Murakami, Y
Poch, O
Biermann, E
Knippers, R
Bréchot, C
Paterlini-Bréchot, P
机构
[1] Fac Med Necker Enfants Malad, INSERM, Unit 370, Inst Pasteur, F-75730 Paris, France
[2] CNRS, Inst Biol Mol & Cellulaire, PUPR 9005, F-67084 Strasbourg, France
[3] Univ Konstanz, Dept Biol, D-78457 Constance, Germany
关键词
D O I
10.1093/nar/gkg136
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
The six minichromosome maintenance proteins (Mcm2-7) are required for both the initiation and elongation of chromosomal DNA, ensuring that DNA replication takes place once, and only once, during the S phase. Here we report on the cloning of a new human Mcm gene (hMcm8) and on characterisation of its protein product. The hMcm8 gene contains the central Mcm domain conserved in the Mcm2-7 gene family, and is expressed in a range of cell lines and human tissues. hMcm8 mRNA accumulates during G(1)/S phase, while hMcm8 protein is detectable throughout the cell cycle. Immunoprecipitation-based studies did not reveal any participation of hMcm8 in the Mcm3/5 and Mcm2/4/6/7 subcomplexes. hMcm8 localises to the nucleus, although it is devoid of a nuclear localisation signal, suggesting that it binds to a nuclear protein. In the nucleus, the hMcm8 structure-bound fraction is detectable in S, but not in G(2)/M, phase, as for hMcm3. However, unlike hMcm3, the hMcm8 structure-bound fraction is not detectable in G(1) phase. Overall, our data identify a new Mcm protein, which does not form part of the Mcm2-7 complex and which is only structure-bound during S phase, thus suggesting its specific role in DNA replication.
引用
收藏
页码:570 / 579
页数:10
相关论文
共 50 条
[41]  
Stoeber K, 2001, J CELL SCI, V114, P2027
[42]   FISSION YEAST MINICHROMOSOME LOSS MUTANTS MIS CAUSE LETHAL ANEUPLOIDY AND REPLICATION ABNORMALITY [J].
TAKAHASHI, K ;
YAMADA, H ;
YANAGIDA, M .
MOLECULAR BIOLOGY OF THE CELL, 1994, 5 (10) :1145-1158
[43]   DbClustal: rapid and reliable global multiple alignments of protein sequences detected by database searches [J].
Thompson, JD ;
Plewniak, F ;
Thierry, JC ;
Poch, O .
NUCLEIC ACIDS RESEARCH, 2000, 28 (15) :2919-2926
[44]   BM28, A HUMAN MEMBER OF THE MCM2-3-5 FAMILY, IS DISPLACED FROM CHROMATIN DURING DNA-REPLICATION [J].
TODOROV, IT ;
ATTARAN, A ;
KEARSEY, SE .
JOURNAL OF CELL BIOLOGY, 1995, 129 (06) :1433-1445
[45]  
Todovov IT, 1998, LAB INVEST, V78, P73
[46]   HsMCM6: A new member of the human MCM/P1 family encodes a protein homologous to fission yeast Mis5 [J].
Tsuruga, H ;
Yabuta, N ;
Hosoya, S ;
Tamura, K ;
Endo, Y ;
Nojima, H .
GENES TO CELLS, 1997, 2 (06) :381-399
[47]   Insights into DNA replication from the third domain of life [J].
Tye, BK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (06) :2399-2401
[48]   MCM proteins in DNA replication [J].
Tye, BK .
ANNUAL REVIEW OF BIOCHEMISTRY, 1999, 68 :649-686
[49]   MCM2 AND MCM3, 2 PROTEINS IMPORTANT FOR ARS ACTIVITY, ARE RELATED IN STRUCTURE AND FUNCTION [J].
YAN, H ;
GIBSON, S ;
TYE, BK .
GENES & DEVELOPMENT, 1991, 5 (06) :944-957
[50]  
Yankulov K, 1999, MOL CELL BIOL, V19, P6154