Liu D F, el-Alfy M, Leblond C P
Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
Anat Rec. 1995 Aug;242(4):449-61. doi: 10.1002/ar.1092420403.
Since it has been found that new chromatin structures make their appearance in the nucleus during the DNA-synthesizing or S phase of the cell cycle, the question arises as to how these structures are related to the nascent DNA.
DNA-containing structures were detected in sections of mouse duodenal crypt cells by the DNA-specific osmium-ammine procedure. In the same sections, the nascent or newly-replicated DNA was localized during stages I-IV of the cell cycle (corresponding to four successive parts of the S phase) by immunogold labeling of the DNA precursor bromodeoxyuridine (BrdU) in mice sacrificed 10 min after its injection. Moreover, the fate of the nascent DNA with time was traced up to 6 hr after the injection. (The nomenclature of the DNA-containing structures is that proposed by El-Alfy et al., 1995.)
Ten minutes after BrdU injection, the gold particles indicative of nascent DNA are associated with discrete nucleofilaments scattered in the nucleoplasm, but not with the compacted nucleofilaments making up the heterochromatin or the new S phase structures named "aggregates." The gold-particle-associated discrete nucleofilaments are classified into three types: a) The "free" nucleofilaments have been given this name, since they appear to be independent of heterochromatin and aggregates; nearly all gold particles are over these at stage I; but the numbers of particles over them decreases from stage I to IV. b) The "aggregate-attached" nucleofilaments project from the surface of the aggregates; the number of particles over these is high at stages II and III but decreases at stage IV. c) The "heterochromatin-attached" nucleofilaments project from the surface of the heterochromatin; the number of particles over these increases from stage II to IV. By 1 hr after BrdU injection, gold particles can be over loose clumps of nucleofilaments at stages I and II, but are mostly over small aggregates at stage II, midsized aggregates and small heterochromatin-associated "bulges" at stage III and large aggregates and large bulges at stage IV. By 2-6 hr, virtually all particles are over aggregates and bulges, frequently deep within them.
The distribution of the gold particles at 10 min reveals that DNA is synthesized in discrete nucleofilaments that are "free" or "aggregate-attached" or "heterochromatin-attached." In contrast, by one and especially two hours, the gold particles are present over aggregates and bulges, indicating that, after discrete nucleofilaments acquire nascent DNA, they are displaced to become part of these structures. More precisely, the aggregates arise from the repeated addition of replicated portions of "free" nucleofilaments, while the bulges arise from the repeated addition of replicated portions, of "heterochromatin-attached" nucleofilaments. Aggregates and bulges are the two initial building stones from which mitotic chromosomes are eventually formed.
自从发现在细胞周期的DNA合成期即S期,细胞核中会出现新的染色质结构以来,就产生了这些结构如何与新生DNA相关的问题。
通过DNA特异性锇胺法在小鼠十二指肠隐窝细胞切片中检测含DNA的结构。在同一切片中,通过对注射溴脱氧尿苷(BrdU)10分钟后处死的小鼠中的DNA前体进行免疫金标记,在细胞周期的I-IV期(对应于S期的四个连续部分)定位新生或新复制的DNA。此外,在注射后长达6小时追踪新生DNA随时间的命运。(含DNA结构的命名法是由El-Alfy等人于1995年提出的。)
BrdU注射10分钟后,指示新生DNA的金颗粒与散布在核质中的离散核丝相关,但与构成异染色质的紧密核丝或名为“聚集体”的新S期结构无关。与金颗粒相关的离散核丝分为三种类型:a)“游离”核丝之所以如此命名,是因为它们似乎独立于异染色质和聚集体;在I期几乎所有金颗粒都在这些核丝上;但在它们上面的颗粒数量从I期到IV期减少。b)“附着于聚集体”的核丝从聚集体表面伸出;在II期和III期这些核丝上的颗粒数量很多,但在IV期减少。c)“附着于异染色质”的核丝从异染色质表面伸出;在这些核丝上的颗粒数量从II期到IV期增加。BrdU注射1小时后,金颗粒在I期和II期可位于松散的核丝团块上,但在II期大多位于小聚集体上,在III期位于中等大小的聚集体和与异染色质相关的小“凸起”上,在IV期位于大聚集体和大凸起上。到2-6小时,几乎所有颗粒都位于聚集体和凸起上,常常深入其中。
10分钟时金颗粒的分布表明DNA在“游离”、“附着于聚集体”或“附着于异染色质”的离散核丝中合成。相比之下,到1小时尤其是2小时后,金颗粒出现在聚集体和凸起上,这表明离散核丝获得新生DNA后,它们移位成为这些结构的一部分。更确切地说,聚集体由“游离”核丝的复制部分重复添加形成,而凸起由“附着于异染色质”的核丝的复制部分重复添加形成。聚集体和凸起是最终形成有丝分裂染色体的两个初始基石。