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真核生物DNA复制

Eukaryotic DNA replication.

作者信息

Wang T A, Li J J

机构信息

Department of Biochemistry, University of California, San Francisco 94143-0448, USA.

出版信息

Curr Opin Cell Biol. 1995 Jun;7(3):414-20. doi: 10.1016/0955-0674(95)80098-0.

DOI:10.1016/0955-0674(95)80098-0
PMID:7662373
Abstract

Recent discoveries suggest that the initiation of eukaryotic DNA replication involves at least two steps--one occurring near the completion of mitosis and the other at the onset of S phase--that bring about the ordered assembly of initiator proteins at the origin. The identification and characterization of components involved in promoting or antagonizing each of these steps has provided a preliminary understanding of how replication initiation is regulated so precisely during the cell cycle.

摘要

最近的发现表明,真核生物DNA复制的起始至少涉及两个步骤——一个发生在有丝分裂接近完成时,另一个发生在S期开始时——这导致起始蛋白在起始点有序组装。对促进或拮抗这些步骤中每一个步骤的成分的鉴定和表征,为初步了解细胞周期中复制起始是如何被精确调控提供了帮助。

相似文献

1
Eukaryotic DNA replication.真核生物DNA复制
Curr Opin Cell Biol. 1995 Jun;7(3):414-20. doi: 10.1016/0955-0674(95)80098-0.
2
Eukaryotic DNA replication.
Curr Opin Cell Biol. 1994 Jun;6(3):368-72. doi: 10.1016/0955-0674(94)90028-0.
3
Eukaryotic DNA replication.真核生物DNA复制
Annu Rev Biochem. 1986;55:733-71. doi: 10.1146/annurev.bi.55.070186.003505.
4
Intergenic DNA and the sequence requirements for replication initiation in eukaryotes.基因间DNA与真核生物复制起始的序列要求。
Curr Opin Genet Dev. 1994 Apr;4(2):196-202. doi: 10.1016/s0959-437x(05)80045-0.
5
Two steps in the assembly of complexes at yeast replication origins in vivo.体内酵母复制起点处复合物组装的两个步骤。
Cell. 1994 Jul 29;78(2):303-16. doi: 10.1016/0092-8674(94)90299-2.
6
DNA replication initiation.DNA复制起始
Methods Mol Biol. 2009;521:3-17. doi: 10.1007/978-1-60327-815-7_1.
7
The dynamics of eukaryotic replication initiation: origin specificity, licensing, and firing at the single-molecule level.真核生物复制起始的动力学:单分子水平上的起始点特异性、许可和激活
Mol Cell. 2015 May 7;58(3):483-94. doi: 10.1016/j.molcel.2015.03.017. Epub 2015 Apr 23.
8
ATP-dependent recognition of eukaryotic origins of DNA replication by a multiprotein complex.一种多蛋白复合物对真核生物DNA复制起点的ATP依赖性识别。
Nature. 1992 May 14;357(6374):128-34. doi: 10.1038/357128a0.
9
The replicon model and eukaryotic chromosomes.
Cold Spring Harb Symp Quant Biol. 1993;58:435-42. doi: 10.1101/sqb.1993.058.01.050.
10
Replication and transcription. Silence of the ORCs.复制与转录。起源识别复合体的沉默。
Curr Biol. 1994 Mar 1;4(3):238-41. doi: 10.1016/s0960-9822(00)00053-1.

引用本文的文献

1
Cell cycle control of Cdc7p kinase activity through regulation of Dbf4p stability.通过调控Dbf4p稳定性实现对Cdc7p激酶活性的细胞周期控制。
Mol Cell Biol. 1999 Jul;19(7):4888-96. doi: 10.1128/MCB.19.7.4888.
2
In vitro chromatin remodelling by chromatin accessibility complex (CHRAC) at the SV40 origin of DNA replication.染色质可及性复合物(CHRAC)在SV40 DNA复制起点处的体外染色质重塑。
EMBO J. 1998 Jun 15;17(12):3428-38. doi: 10.1093/emboj/17.12.3428.
3
Cell cycle modulation of protein-DNA interactions at a human replication origin.
人类复制起点处蛋白质 - DNA 相互作用的细胞周期调控
EMBO J. 1998 May 15;17(10):2961-9. doi: 10.1093/emboj/17.10.2961.
4
CDC45 is required in conjunction with CDC7/DBF4 to trigger the initiation of DNA replication.CDC45需要与CDC7/DBF4协同作用来触发DNA复制的起始。
Proc Natl Acad Sci U S A. 1997 Nov 11;94(23):12521-6. doi: 10.1073/pnas.94.23.12521.
5
CDC45, a novel yeast gene that functions with the origin recognition complex and Mcm proteins in initiation of DNA replication.CDC45,一种新型酵母基因,在DNA复制起始过程中与起始识别复合物和Mcm蛋白共同发挥作用。
Mol Cell Biol. 1997 Feb;17(2):553-63. doi: 10.1128/MCB.17.2.553.
6
Establishing genetic interactions by a synthetic dosage lethality phenotype.通过合成剂量致死表型建立基因相互作用。
Genetics. 1996 May;143(1):95-102. doi: 10.1093/genetics/143.1.95.
7
Yeast pip3/mec3 mutants fail to delay entry into S phase and to slow DNA replication in response to DNA damage, and they define a functional link between Mec3 and DNA primase.酵母pip3/mec3突变体在响应DNA损伤时无法延迟进入S期并减缓DNA复制,它们定义了Mec3与DNA引发酶之间的功能联系。
Mol Cell Biol. 1996 Jul;16(7):3235-44. doi: 10.1128/MCB.16.7.3235.
8
cdc18+ regulates initiation of DNA replication in Schizosaccharomyces pombe.cdc18+调节粟酒裂殖酵母中的DNA复制起始。
Proc Natl Acad Sci U S A. 1996 Feb 20;93(4):1566-70. doi: 10.1073/pnas.93.4.1566.