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[人类细胞S期细胞核中DNA复制结构域的组织]

[Organization of DNA replication domains in S-phase nuclei of human cells].

作者信息

Solovjeva L V, Tomilin A N, Rozanov Iu M, Pleskach N M, Chagin V O, Tomilin N V

机构信息

Institute of Cytology, Russian Academy of Sciences, St. Petersburg.

出版信息

Tsitologiia. 1998;40(8-9):779-85.

PMID:9821249
Abstract

Each chromosome of eukaryotic cells contains multiple units of DNA replication that are activated during S-phase of cell cycle according to a definite program. It is considered at present that the main independent units of replication in mammalian cells represent groups of 20-25 adjacent synchronously activated small (with the average size 100 kbp) replicons. After labelling of nascent DNA with nonradioactive DNA precursors and immunofluorescent staining of incorporated label, discrete replication domains (RDs) are detected in S-phase nuclei. It is assumed that each RD is formed by a single group of synchronously activated small replicons. Since the average rate of replication fork movement is 2 kbp/min, a group of small replicons should finish DNA synthesis within 25 min, and only during this time one RD should incorporate the replicative label. We have studied the duration of DNA synthesis in individual RDs in S-phase human cells using double replicative labelling that can be detected in the nucleus by specific reagents. Our results indicate that in the main fraction of RDs DNA synthesis lasts more than 90 min, that contradicts the generally accepted model of organization of replication units in mammalian cells (Hand, 1978), but is in agreement with an alternative model, according to which the main replication units are single or clustered big replicons more than 300 kbp in size (Liapunova, 1994).

摘要

真核细胞的每条染色体都包含多个DNA复制单元,这些复制单元在细胞周期的S期根据特定程序被激活。目前认为,哺乳动物细胞中主要的独立复制单元是由20 - 25个相邻的同步激活的小(平均大小为100 kbp)复制子组成的群体。在用非放射性DNA前体标记新生DNA并对掺入的标记进行免疫荧光染色后,在S期细胞核中检测到离散的复制结构域(RDs)。据推测,每个RD由一组同步激活的小复制子形成。由于复制叉移动的平均速率为2 kbp/分钟,一组小复制子应在25分钟内完成DNA合成,并且只有在此期间一个RD才会掺入复制标记。我们使用可通过特定试剂在细胞核中检测到的双重复制标记,研究了S期人类细胞中单个RDs的DNA合成持续时间。我们的结果表明,在大部分RDs中,DNA合成持续超过90分钟,这与哺乳动物细胞中复制单元组织的普遍接受模型(Hand,1978)相矛盾,但与另一种模型一致,根据该模型,主要的复制单元是单个或成簇的大小超过300 kbp的大复制子(Liapunova,1994)。

相似文献

1
[Organization of DNA replication domains in S-phase nuclei of human cells].[人类细胞S期细胞核中DNA复制结构域的组织]
Tsitologiia. 1998;40(8-9):779-85.
2
[Units of DNA replication in S-phase human cells].[人类细胞S期的DNA复制单位]
Tsitologiia. 1997;39(2-3):138-49.
3
[High resolution analysis of replication foci by conventional fluorescent microscopy. I. A study of complexity and DNA content of the foci].[通过传统荧光显微镜对复制灶进行高分辨率分析。I. 对复制灶的复杂性和DNA含量的研究]
Tsitologiia. 2004;46(3):229-43.
4
[Replicon size and rate of DNA replication in the macronucleus of Tetrahymena pyriformis].[梨形四膜虫大核中的复制子大小与DNA复制速率]
Tsitologiia. 1979 Mar;21(3):318-26.
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Nuclear matrix support of DNA replication.DNA复制的核基质支持
J Cell Biochem. 2005 Dec 1;96(5):951-61. doi: 10.1002/jcb.20610.
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[Organization of mammalian genome replication: data on the high rate of DNA replication in replicons of structural heterochromatin].[哺乳动物基因组复制的组织:关于结构异染色质复制子中DNA高复制率的数据]
Tsitologiia. 1980 Jun;22(6):640-5.
7
DNA replication fork progression rate and temporal organization of S phase in normal epidermis and in basal cell carcinoma.正常表皮和基底细胞癌中DNA复制叉进展速率及S期的时间组织
J Cell Physiol. 1988 Nov;137(2):374-7. doi: 10.1002/jcp.1041370223.
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Mimosine arrests proliferating human cells before onset of DNA replication in a dose-dependent manner.含羞草氨酸以剂量依赖的方式在DNA复制开始前阻止人类增殖细胞。
Exp Cell Res. 1999 Feb 25;247(1):148-59. doi: 10.1006/excr.1998.4342.
9
Developing a model of DNA replication to be used for Monte Carlo calculations that predict the sizes and shapes of molecules resulting from DNA double-strand breaks induced by X irradiation during DNA synthesis.开发一种DNA复制模型,用于蒙特卡罗计算,以预测DNA合成过程中X射线诱导的DNA双链断裂所产生的分子大小和形状。
Radiat Res. 1997 Nov;148(5):421-34.
10
Replicon clusters are stable units of chromosome structure: evidence that nuclear organization contributes to the efficient activation and propagation of S phase in human cells.复制子簇是染色体结构的稳定单位:有证据表明核组织有助于人类细胞中S期的有效激活和传播。
J Cell Biol. 1998 Mar 23;140(6):1285-95. doi: 10.1083/jcb.140.6.1285.

引用本文的文献

1
A method to monitor replication fork progression in mammalian cells: nucleotide excision repair enhances and homologous recombination delays elongation along damaged DNA.一种监测哺乳动物细胞中复制叉进展的方法:核苷酸切除修复增强,同源重组延迟沿受损DNA的延伸。
Nucleic Acids Res. 2004 Nov 10;32(20):e157. doi: 10.1093/nar/gnh154.
2
Multiple deceleration of DNA synthesis during the S phase of cell cycle: study by flow cytometry method.
Dokl Biochem Biophys. 2004 Jan-Feb;394:11-4. doi: 10.1023/b:dobi.0000017143.87464.0f.