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在经锇氨染色的小鼠十二指肠隐窝细胞中观察到的与中期染色体形成相关的DNA变化。I. 新结构在S期出现,并在前期浓缩成“染色粒”,这些染色粒在 prometaphase融合形成有丝分裂染色体。

DNA changes involved in the formation of metaphase chromosomes, as observed in mouse duodenal crypt cells stained by osmium-ammine. I. New structures arise during the S phase and condense at prophase into "chromomeres," which fuse at prometaphase into mitotic chromosomes.

作者信息

el-Alfy M, Liu D F, Leblond C P

机构信息

Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.

出版信息

Anat Rec. 1995 Aug;242(4):433-48. doi: 10.1002/ar.1092420402.

Abstract

BACKGROUND

In the hope of understanding how chromosomes condense at mitosis, we took advantage of a subdivision of the cell cycle into 11 stages to examine the changes in DNA taking place during the stages preceding the emergence of metaphase chromosomes.

METHODS

To identify DNA changes, pieces of mouse duodenum were fixed in formaldehyde, and sections of the rapidly dividing cells of the crypts were stained by the osmium-ammine method, which is specific for the detection of DNA in the electron microscope.

RESULTS

Throughout the cell cycle, DNA is present in nucleofilaments composed of rows of 11-nm-wide nucleosomes. At stage I, during which the DNA-synthesizing or S phase of the cell cycle begins, some of the nucleofilaments are compacted in the heterochromatin accumulations associated with nuclear envelope and nucleoli, while the others are scattered in the nucleoplasm where they appear either "free" or "attached" to the heterochromatin. This DNA distribution is similar to that observed in the noncycling cells examined. After the beginning of the S phase, "free" nucleofilaments are seen to assemble into structures composed of compacted nucleofilaments and referred to as "aggregates"; these make their appearance at stage II and increase in size through stage III up to the end of S during stage IV. Meanwhile, the heterochromatin associated with nuclear envelope and nucleoli expands toward the nucleoplasm in the form of protrusions referred to as "bulges," which gradually enlarge during stages III and IV, while the heterochromatin shrinks and eventually vanishes. On average, a total of 1,171 aggregates and bulges are formed in the nucleus during the S phase. At the apparition of stage V, which corresponds approximately to prophase, aggregates and bulges are rapidly gathered into an average of 288 spheroidal bodies referred to as "chromomeres." These are connected to one another by nucleofilamentous bridges in such a way as to be lined up in rows. The formation of rows of chromomeres represents in the electron microscope the prophasic condensation observed in the light microscope. Finally, during stage VIa, which corresponds to prometaphase, the chromomeres approach one another within each row, make contact, and coalesce to become the 40 chromosomes of the mouse, which during stage VIb are organized in the equatorial plate of metaphase.

CONCLUSIONS

The condensation of metaphase chromosomes occurs in three main steps. The first and longest takes place during the S phase, as nucleofilaments are assembled into aggregates, while the heterochromatin gives rise to bulges. The brief second step occurs toward the beginning of prophase, when the numerous aggregates and bulges are congregated into a limited number of chromomeres, which are lined up in rows. The third step takes place during the brief prometaphase, when the chromomeres of a row coalesce into a mitotic chromosome.

摘要

背景

为了了解染色体在有丝分裂时如何浓缩,我们利用细胞周期可细分为11个阶段这一特点,来研究中期染色体出现之前各阶段DNA发生的变化。

方法

为了识别DNA的变化,将小鼠十二指肠组织块用甲醛固定,隐窝中快速分裂细胞的切片用锇氨法染色,该方法在电子显微镜下对检测DNA具有特异性。

结果

在整个细胞周期中,DNA存在于由一排排11纳米宽的核小体组成的核丝中。在阶段I,即细胞周期的DNA合成期或S期开始时,一些核丝在与核膜和核仁相关的异染色质聚集体中被压缩,而其他核丝则散布在核质中,在那里它们看起来要么“游离”,要么“附着”于异染色质。这种DNA分布与在检查的非循环细胞中观察到的相似。S期开始后,可见“游离”核丝组装成由压缩核丝组成的结构,称为“聚集体”;这些聚集体在阶段II出现,并在阶段III增大尺寸,直至阶段IV的S期末。与此同时,与核膜和核仁相关的异染色质以称为“凸起”的突起形式向核质扩展,在阶段III和IV逐渐增大,而异染色质收缩并最终消失。在S期,细胞核中平均共形成1171个聚集体和凸起。在大约对应于前期的阶段V出现时,聚集体和凸起迅速聚集形成平均288个称为“染色粒”的球状小体。它们通过核丝状桥相互连接,从而排成行。在电子显微镜下,一排排染色粒的形成代表了在光学显微镜下观察到的前期浓缩。最后,在对应于前中期的阶段VIa,染色粒在每一排内彼此靠近、接触并合并,成为小鼠的40条染色体,在阶段VIb这些染色体排列在中期的赤道板上。

结论

中期染色体的浓缩发生在三个主要步骤。第一个也是最长的步骤发生在S期,核丝组装成聚集体,而异染色质产生凸起。第二个短暂步骤发生在前期开始时,大量聚集体和凸起聚集形成数量有限的染色粒,并排成行。第三个步骤发生在短暂的前中期,一排染色粒合并成一条有丝分裂染色体。

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