de Laat Wouter, Grosveld Frank
Department of Cell Biology and Genetics, Faculty of Medicine, Erasmus University, Rotterdam, PO Box 1738, 3000DR Rotterdam, The Netherlands.
Chromosome Res. 2003;11(5):447-59. doi: 10.1023/a:1024922626726.
Developmental and tissue-specific expression of higher eukaryotic genes involves activation of transcription at the appropriate time and place and keeping it silent otherwise. Unlike housekeeping genes, tissue-specific genes generally do not cluster on the chromosomes. They can be found in gene-dense regions of chromosomes as well as in regions of repressive chromatin. Depending on the location, shielding against positive or negative regulatory effects from neighboring chromatin may be required and hence insulator and boundary models were proposed. They postulate that chromosomes are partitioned into physically distinct expression domains, each containing a gene or gene cluster with its cis-regulatory elements. Specialized elements at the borders of such domains are proposed to prevent cross-talk between domains, and thus to be crucial in establishing independent expression domains. However, genes and associated cis-acting sequences often do not occupy physically distinct domains on the chromosomes. Rather, genes can overlap and cis-acting sequences can be found tens or hundreds of kilobases away from the target gene, sometimes with unrelated genes in between. Therefore the ability of a gene to communicate with positive cis-regulatory elements rather than the presence of specialized boundary elements appears to be key to establishing an independent expression profile. Our recent finding that active beta-globin genes physically interact in the nuclear space with multiple cis-regulatory elements, with inactive genes looping out, has provided a potential mechanistic framework for this model. We refer to such a spatial unit of regulatory DNA elements as an active chromatin hub (ACH). We propose that productive ACH formation underlies correct gene expression, requiring the presence of protein factors with the appropriate affinities for each other bound to their cognate DNA sequences. Proximity and specificity determines which cis-acting sequences and promoter(s) form an ACH, and thus which gene will be expressed. Other regulatory sequences can interfere with transcription by blocking the appropriate physical interaction between an enhancer and promoter in the ACH. Possible mechanisms by which distal DNA elements encounter each other in the 3D nuclear space will be discussed.
高等真核生物基因的发育和组织特异性表达涉及在适当的时间和地点激活转录,并在其他情况下保持沉默。与管家基因不同,组织特异性基因通常不在染色体上成簇分布。它们可以在染色体的基因密集区域以及抑制性染色质区域中找到。根据位置的不同,可能需要屏蔽来自相邻染色质的正向或负向调节作用,因此提出了绝缘子和边界模型。这些模型假定染色体被划分为物理上不同的表达结构域,每个结构域包含一个基因或基因簇及其顺式调节元件。有人提出,这些结构域边界处的特殊元件可防止结构域之间的串扰,因此对于建立独立的表达结构域至关重要。然而,基因和相关的顺式作用序列在染色体上通常并不占据物理上不同的结构域。相反,基因可能会重叠,顺式作用序列可能在距离靶基因数十或数百千碱基处被发现,有时中间还夹杂着不相关的基因。因此,基因与正向顺式调节元件进行交流的能力而非特殊边界元件的存在,似乎是建立独立表达谱的关键。我们最近的发现,即活跃的β-珠蛋白基因在核空间中与多个顺式调节元件发生物理相互作用,而不活跃的基因则呈环状突出,为该模型提供了一个潜在的机制框架。我们将这种调节性DNA元件的空间单元称为活性染色质枢纽(ACH)。我们提出,有效的ACH形成是正确基因表达的基础,这需要存在对彼此具有适当亲和力并结合到其同源DNA序列上的蛋白质因子。接近度和特异性决定了哪些顺式作用序列和启动子形成一个ACH,从而决定了哪个基因将被表达。其他调节序列可通过阻断ACH中增强子与启动子之间适当的物理相互作用来干扰转录。本文将讨论远端DNA元件在三维核空间中相互接触的可能机制。