Benbow R M
Department of Zoology and Genetics, Iowa State University, Ames 50011-3260.
Sci Prog. 1992;76(301-302 Pt 3-4):425-50.
Chromosomes are large subcellular structures, visible in the light microscope, that are found in the nuclei of most eukaryotic cells. Each chromosome consists of a single very long DNA molecule that has been compacted approximately 10,000-fold by interactions with proteins, such that the resulting chromosome structure fits within a typical eukaryotic nucleus of only 10 microns in diameter. Several levels of structural organisation are involved in the formation of chromosomes. Most chromosomal DNA is wrapped in left-handed superhelical turns around protein 'spools', called histone octamers, to form nucleosomes. Arrays of these nucleosomes, or 'beads on a string', are further compacted into solenoidal structures, called 30 nm chromatin fibres. The chromatin fibres are, in turn, compacted approximately 250-fold to form topologically independent 'looped' DNA domains, each loop containing about 20,000-100,000 nucleotide pairs of DNA extending from a proteinaceous central scaffold. Some chromosomes, such as lampbrush and polytene chromosomes, can be seen in certain specialised cells during interphase. Metaphase chromosomes, which can be stained to reveal characteristic banding patterns, are formed in most eukaryotic cells during mitosis. Formation of chromosome structures and the nuclei that envelop them involves discrete steps of nucleosome assembly, scaffold assembly, and nuclear envelope assembly, and can be carried out in cell-free extracts of animal eggs. Centromeres, the regions that mediate attachment of a chromosome to a meiotic or mitotic spindle, and telomeres, the natural ends of chromosomes, are structures that ensure that the correct number of full length chromosomes are maintained during the cell cycle. Most chromosome structures (nucleosomes, chromatin fibres, and scaffold loop domains) form from virtually any DNA sequence, but centromeres and telomeres are both composed of specific DNA sequences complexed with specific binding proteins. Recently, complete DNA sequences of entire chromosomes have been determined, and our rapidly emerging knowledge of chromosome structures is beginning to provide insights into the molecular basis of human disease.
染色体是大型亚细胞结构,在光学显微镜下可见,存在于大多数真核细胞的细胞核中。每条染色体由单个非常长的DNA分子组成,该分子通过与蛋白质相互作用而被压缩了约10000倍,从而使形成的染色体结构能够容纳在直径仅为10微米的典型真核细胞核内。染色体的形成涉及多个结构组织层次。大多数染色体DNA以左手超螺旋形式缠绕在称为组蛋白八聚体的蛋白质“线轴”上,形成核小体。这些核小体阵列,即“串珠”,进一步压缩成螺线管结构,称为30纳米染色质纤维。染色质纤维又被压缩约250倍,形成拓扑独立的“环状”DNA结构域,每个环包含从蛋白质中心支架延伸出的约20000 - 100000个核苷酸对的DNA。在某些特殊细胞的间期可以看到一些染色体,如灯刷染色体和多线染色体。在有丝分裂期间,大多数真核细胞中会形成中期染色体,可对其进行染色以揭示特征性的带型模式。染色体结构及其周围细胞核的形成涉及核小体组装、支架组装和核膜组装等离散步骤,并且可以在动物卵细胞的无细胞提取物中进行。着丝粒是介导染色体与减数分裂或有丝分裂纺锤体附着的区域,端粒是染色体的天然末端,它们是确保在细胞周期中维持正确数量的全长染色体的结构。大多数染色体结构(核小体、染色质纤维和支架环结构域)几乎可以由任何DNA序列形成,但着丝粒和端粒都由与特定结合蛋白复合的特定DNA序列组成。最近,已经确定了整条染色体的完整DNA序列,我们对染色体结构的快速增长的认识开始为人类疾病的分子基础提供见解。