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Identification and functional characterization of a new member of the human Mcm protein family: hMcm8
Author(s) -
Devrim Gözüaçık,
Mounia Chami,
David Lagorce,
Jamila Faivre,
Yoshiki Murakami,
Olivier Poch,
Esther Biermann,
Rolf Knippers,
Christian Bréchot,
Patrizia Paterlini-Bréchot
Publication year - 2003
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkg136
Subject(s) - biology , minichromosome maintenance , nuclear protein , dna replication , immunoprecipitation , origin recognition complex , microbiology and biotechnology , minichromosome , gene , nuclear localization sequence , genetics , dna , eukaryotic dna replication , chromatin , transcription factor
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.

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