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本文引用的文献

1
Translocation of a UV-damaged DNA binding protein into a tight association with chromatin after treatment of mammalian cells with UV light.用紫外线处理哺乳动物细胞后,一种紫外线损伤的DNA结合蛋白易位并与染色质紧密结合。
J Cell Sci. 1997 May;110 ( Pt 10):1159-68. doi: 10.1242/jcs.110.10.1159.
2
UV damage and repair mechanisms in mammalian cells.哺乳动物细胞中的紫外线损伤与修复机制
Bioessays. 1996 Mar;18(3):221-8. doi: 10.1002/bies.950180309.
3
Chromatin diminution in nematodes.线虫中的染色质消减
Bioessays. 1996 Feb;18(2):133-8. doi: 10.1002/bies.950180209.
4
DNA repair in eukaryotes.真核生物中的DNA修复
Annu Rev Biochem. 1996;65:135-67. doi: 10.1146/annurev.bi.65.070196.001031.
5
Mutations specific to the xeroderma pigmentosum group E Ddb- phenotype.着色性干皮病E组Ddb-表型特有的突变。
J Biol Chem. 1996 Oct 4;271(40):24317-20. doi: 10.1074/jbc.271.40.24317.
6
HHR23B, a human Rad23 homolog, stimulates XPC protein in nucleotide excision repair in vitro.HHR23B是一种人类Rad23同源物,在体外核苷酸切除修复过程中可刺激XPC蛋白。
Mol Cell Biol. 1996 Sep;16(9):4852-61. doi: 10.1128/MCB.16.9.4852.
7
Boveri's contributions to developmental biology--a challenge for today.博韦里对发育生物学的贡献——当今面临的一项挑战。
Int J Dev Biol. 1996 Feb;40(1):27-47.
8
Overproduction, purification, and characterization of the XPC subunit of the human DNA repair excision nuclease.人DNA修复切除核酸酶XPC亚基的过量表达、纯化及特性分析
J Biol Chem. 1996 Aug 9;271(32):19451-6. doi: 10.1074/jbc.271.32.19451.
9
Evidence for a novel DNA damage binding protein in human cells.人类细胞中一种新型DNA损伤结合蛋白的证据。
Proc Natl Acad Sci U S A. 1996 Jul 9;93(14):6918-23. doi: 10.1073/pnas.93.14.6918.
10
Purification of a novel UV-damaged-DNA binding protein highly specific for (6-4) photoproduct.一种对(6-4)光产物具有高度特异性的新型紫外线损伤DNA结合蛋白的纯化。
Nucleic Acids Res. 1996 Mar 15;24(6):1099-04. doi: 10.1093/nar/24.6.1099.

一种新型的紫外线损伤DNA结合蛋白在猪蛔虫染色质消除裂解期出现。

A novel UV-damaged DNA binding protein emerges during the chromatin-eliminating cleavage period in Ascaris suum.

作者信息

Seidl C, Moritz K B

机构信息

Zoologisches Institut der Universität, Luisenstrasse 14, 80333 München, Germany.

出版信息

Nucleic Acids Res. 1998 Feb 1;26(3):768-77. doi: 10.1093/nar/26.3.768.

DOI:10.1093/nar/26.3.768
PMID:9443969
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC147329/
Abstract

During the early cleavage period of Ascaris suum , chromatin diminution takes place in the somatic founder cells. In the process of chromatin diminution numerous heterochromatic blocks, consisting predominantly of highly repeated DNA, are discarded during mitotic anaphase and are later on digested in the cytoplasm. Very little is known about proteins that are involved in chromatin diminution. We have detected a nuclear protein and purified it to near homogeneity by its preferential binding to UV-damaged DNA. We termed this protein chromatin diminution associated factor 1 (CDAF1), because maximum binding activity per nucleus was observed to develop in 4-8-cell stages, when chromatin diminution occurs for the first time. CDAF1 recognizes cyclobutane pyrimidine dimers in UV-damaged double-stranded DNA. Its binding properties identify CDAF1 as a novel kind of damaged-DNA binding protein. CDAF1 activity is almost not detectable in 1-celled embryos. It increases dramatically during formation of somatic founder cells and persists up to the first larval stage. However, CDAF1 is absent in tissues of adults. These findings led us to suggest that CDAF1 plays a dual role: during the early segregative cleavage period it might be involved in chromatin diminution as a transfactor and act in nucleotide excision repair as an accessory factor throughout embryogenesis.

摘要

在猪蛔虫的早期卵裂期,染色质消减发生在体细胞的起始细胞中。在染色质消减过程中,许多主要由高度重复DNA组成的异染色质块在有丝分裂后期被丢弃,随后在细胞质中被消化。关于参与染色质消减的蛋白质,人们了解甚少。我们检测到一种核蛋白,并通过其与紫外线损伤DNA的优先结合将其纯化至接近同质状态。我们将这种蛋白质称为染色质消减相关因子1(CDAF1),因为在首次发生染色质消减的4-8细胞阶段,每个细胞核的最大结合活性被观察到开始出现。CDAF1识别紫外线损伤的双链DNA中的环丁烷嘧啶二聚体。其结合特性将CDAF1鉴定为一种新型的损伤DNA结合蛋白。在单细胞胚胎中几乎检测不到CDAF1的活性。在体细胞起始细胞形成过程中,它急剧增加,并持续到第一幼虫阶段。然而,在成虫组织中不存在CDAF1。这些发现使我们认为CDAF1具有双重作用:在早期的分离卵裂期,它可能作为一种反式因子参与染色质消减,并在整个胚胎发育过程中作为辅助因子参与核苷酸切除修复。