Norris Vic, Demarty Maurice, Raine Derek, Cabin-Flaman Armelle, Le Sceller Loïs
Laboratoire des processus intégratifs cellulaires, UPRESA CNRS 6037, faculté des sciences et techniques, université de Rouen, 76821 cedex, Mont-Saint-Aignan, France.
Biochimie. 2002 Apr;84(4):341-7. doi: 10.1016/s0300-9084(02)01387-1.
Hyperstructures or modules have been proposed to constitute a level of organisation intermediate between macromolecules and whole cells. In this model of intracellular organisation, hyperstructures compete and collaborate for existence within the membrane and cytoplasm. Those directly involved in the cell cycle include initiation, replication and division hyperstructures based on DnaA, SeqA and the 2-minute cluster, respectively. During the run-up to initiation, the mass to DNA ratio increases and, we contend, differential gene expression leads to some hyperstructures becoming more active and stable than others. This results in a drop in the diversity of hyperstructures, some of which release DnaA as they dissociate, and a DnaA-initiation hyperstructure forms. Subsequent DNA replication and cell division generate different daughter cells containing different hyperstructures. This has the advantage of increasing the phenotypic diversity of the population. In developing this model, we also invoke hyperstructures in the partitioning of origins of replication.
超结构或模块被认为构成了介于大分子和整个细胞之间的一个组织层次。在这种细胞内组织模型中,超结构在膜和细胞质内为生存而竞争与协作。那些直接参与细胞周期的超结构分别包括基于DnaA、SeqA和2分钟簇的起始、复制和分裂超结构。在起始前期,质量与DNA的比率增加,并且我们认为,差异基因表达导致一些超结构比其他超结构更活跃和稳定。这导致超结构多样性下降,其中一些在解离时释放DnaA,从而形成一个DnaA起始超结构。随后的DNA复制和细胞分裂产生含有不同超结构的不同子细胞。这具有增加群体表型多样性的优势。在开发这个模型时,我们还将超结构引入复制起点的分配过程中。