Faculté de Médecine, INSERM, U823, Université Joseph Fourier - Grenoble, Institut Albert Bonniot, La Tronche Cedex, France.
Syst Biol Reprod Med. 2012 Aug;58(4):191-6. doi: 10.3109/19396368.2012.663055.
During the post-meiotic maturation of the male gamete, the haploid genome undergoes major structural transitions, leading to its extreme compaction in a unique specialized structure. Although this process is highly conserved and crucial for the production of male gametes suitable for procreation, its molecular basis has remained unexplored for many years. In particular, the factors driving these events remain to be discovered. Our group has combined specific proteomic approaches with in silico analyses of available expression and sequence data in order to identify chromatin-associated factors as candidates involved in post meiotic reprogramming of the male genome of mice. Here we survey these approaches and the major results obtained. The systematic identification and the functional characterization of several of these factors has led to the proposal of the first working models, guiding us toward the understanding of this unique and very fundamental process, which has long remained one of the black boxes of modern biology.
在雄性配子的减数分裂后成熟过程中,单倍体基因组经历重大的结构转变,导致其在独特的专门结构中极度紧缩。尽管这个过程高度保守且对产生适合生殖的雄性配子至关重要,但多年来其分子基础仍未被探索。特别是,驱动这些事件的因素仍有待发现。我们的研究小组将特定的蛋白质组学方法与对现有表达和序列数据的计算机分析相结合,以鉴定染色质相关因子作为参与小鼠减数分裂后雄性基因组重编程的候选因子。在这里,我们调查了这些方法和获得的主要结果。这些因素中的几个的系统鉴定和功能特征分析,导致了第一个工作模型的提出,指导我们理解这个独特而非常基础的过程,这个过程长期以来一直是现代生物学的一个黑盒子。