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四膜虫细胞核死亡过程中的DNA消化与染色质浓缩

DNA digestion and chromatin condensation during nuclear death in Tetrahymena.

作者信息

Mpoke S, Wolfe J

机构信息

Department of Biology, Wesleyan University, Middletown, Connecticut 06459, USA.

出版信息

Exp Cell Res. 1996 Jun 15;225(2):357-65. doi: 10.1006/excr.1996.0186.

Abstract

DNA fragmentation and nuclear condensation are key features in the regulated cell death of higher animal cells. Nuclear death also occurs as part of a developmentally programmed process during the sexual life cycle of the unicellular organism Tetrahymena. We examined the regulation of nuclear death and the relationship between DNA fragmentation and chromatin condensation in this model system. Nuclear death is accompanied by DNA digestion to low-molecular-weight oligonucleosomal-length fragments, in agreement with a previous study, indicating an endonuclease-like activity typical of apoptosis in higher organisms. Actinomycin D and cycloheximide block DNA digestion as well as nuclear condensation suggesting that nuclear death is under genetic regulation. DNA digestion is completely blocked by aurin, a general nuclease inhibitor. In addition, when DNA fragmentation is blocked, nuclear condensation also fails to occur. Moreover, a kinetic analysis of DNA breakdown, using agarose gels, shows that some DNA digestion occurs before nuclear condensation has taken place. Thus the initiation of DNA digestion may provide conditions necessary for nuclear condensation. Temporary inhibition of nuclear death aborts the death program since after removal of inhibitors cells revert to a vegetative pathway without having eliminated the old or developed the new macronucleus. Zn2+ and EGTA, both of which inhibit apoptosis in some cell types, fail to prevent nuclear condensation or DNA digestion in Tetrahymena, suggesting a requirement here for an endonuclease which is Ca2+-independent and Zn2+-insensitive. With the TUNEL assay, DNA breakdown is detected exclusively in the condensed macronucleus (and occasional micronuclei identified as degenerating haploid products of meiosis), but not in precondensed macronuclei. These studies show that apoptotic-like DNA fragmentation occurs after condensation of the degenerating macronucleus. However, early DNA digestion may be critical for nuclear condensation and subsequent degeneration.

摘要

DNA片段化和核浓缩是高等动物细胞程序性死亡的关键特征。在单细胞生物四膜虫的有性生活周期中,核死亡也是发育程序性过程的一部分。我们在这个模型系统中研究了核死亡的调控以及DNA片段化与染色质浓缩之间的关系。与之前的一项研究一致,核死亡伴随着DNA被消化成低分子量的寡核小体长度片段,这表明存在高等生物中典型的类似凋亡的内切核酸酶活性。放线菌素D和环己酰亚胺可阻断DNA消化以及核浓缩,这表明核死亡受基因调控。金精三羧酸(一种通用核酸酶抑制剂)可完全阻断DNA消化。此外,当DNA片段化被阻断时,核浓缩也不会发生。而且,使用琼脂糖凝胶对DNA降解进行动力学分析表明,在核浓缩发生之前就已经有一些DNA被消化了。因此,DNA消化的启动可能为核浓缩提供必要条件。暂时抑制核死亡会使死亡程序中止,因为去除抑制剂后,细胞会恢复到营养生长途径,而不会消除旧的大核或发育出新的大核。锌离子(Zn2+)和乙二醇双乙胺醚四乙酸(EGTA)在某些细胞类型中都能抑制凋亡,但它们无法阻止四膜虫中的核浓缩或DNA消化,这表明这里需要一种不依赖钙离子(Ca2+)且对锌离子不敏感的内切核酸酶。通过末端脱氧核苷酸转移酶介导的缺口末端标记法(TUNEL)检测到,DNA降解仅在浓缩的大核(以及偶尔被鉴定为减数分裂退化单倍体产物的微核)中被检测到,而在预浓缩的大核中未被检测到。这些研究表明,类似凋亡的DNA片段化发生在退化大核浓缩之后。然而,早期的DNA消化可能对核浓缩及随后的退化至关重要。

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