Kingston R E, Bunker C A, Imbalzano A N
Department of Molecular Biology, Massachusetts General Hospital, Boston, Massachusetts, 02114, USA.
Genes Dev. 1996 Apr 15;10(8):905-20. doi: 10.1101/gad.10.8.905.
Recent studies have provided strong evidence that macromolecular complexes are used in the cell to remodel chromatin structure during activation and to create an inaccessible structure during repression, Although there is not yet any rigorous demonstration that modification of chromatin structure plays a direct, causal role in either activation or repression, there is sufficient smoke to indicate the presence of a blazing inferno nearby. It is clear that complexes that remodel chromatin are tractable in vitro; hopefully this will allow the establishment of systems that provide a direct analysis of the role that remodeling might play in activation. These studies indicate that establishment of functional systems to corroborate the elegant genetic studies on repression might also be tractable. As the mechanistic effects of these complexes are sorted out, it will become important to understand how the complexes are regulated. In many of the instances discussed above, the genes whose products make up these complexes were identified in genetic screens for effects on developmental processes. This implies a regulation of the activity of these complexes in response to developmental cues and further implies that the work to fully understand these complexes will occupy a generation of scientists.
最近的研究提供了有力证据,表明细胞中利用大分子复合物在激活过程中重塑染色质结构,并在抑制过程中形成难以接近的结构。尽管尚未有任何严格的证据证明染色质结构的修饰在激活或抑制中起直接的因果作用,但已有足够的迹象表明附近存在熊熊烈火。显然,在体外可对重塑染色质的复合物进行研究;有望借此建立一些系统,直接分析重塑在激活过程中可能发挥的作用。这些研究表明,建立功能系统以证实关于抑制的精细遗传学研究也可能是可行的。随着这些复合物的机制效应被梳理清楚,了解这些复合物如何被调控将变得很重要。在上述许多例子中,其产物构成这些复合物的基因是在针对发育过程影响的遗传筛选中被鉴定出来的。这意味着这些复合物的活性受发育信号调控,进一步意味着要全面理解这些复合物,这一工作将耗费一代科学家的精力。