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

D Gozuacik, M Chami, D Lagorce, J Faivre… - Nucleic acids …, 2003 - academic.oup.com
D Gozuacik, M Chami, D Lagorce, J Faivre, Y Murakami, O Poch, E Biermann, R Knippers…
Nucleic acids research, 2003academic.oup.com
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 …
Abstract
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.
Oxford University Press