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1
CENP-B: a major human centromere protein located beneath the kinetochore.着丝粒蛋白B:一种主要的人类着丝粒蛋白,位于动粒下方。
J Cell Biol. 1990 May;110(5):1475-88. doi: 10.1083/jcb.110.5.1475.
2
Visualization of prekinetochore locus on the centromeric region of highly extended chromatin fibers: does kinetochore autoantigen CENP-C constitute a kinetochore organizing center?高度伸展染色质纤维着丝粒区域动粒前体位点的可视化:动粒自身抗原CENP-C是否构成动粒组织中心?
Chromosome Res. 1999;7(1):9-19. doi: 10.1023/a:1009267010071.
3
Specification of kinetochore-forming chromatin by the histone H3 variant CENP-A.组蛋白H3变体CENP-A对动粒形成染色质的特异性。
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4
Centromere/kinetochore localization of human centromere protein A (CENP-A) exogenously expressed as a fusion to green fluorescent protein.作为与绿色荧光蛋白融合体而外源表达的人类着丝粒蛋白A(CENP-A)的着丝粒/动粒定位。
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Identification of novel centromere/kinetochore-associated proteins using monoclonal antibodies generated against human mitotic chromosome scaffolds.利用针对人有丝分裂染色体支架产生的单克隆抗体鉴定新型着丝粒/动粒相关蛋白。
J Cell Biol. 1991 Mar;112(6):1083-97. doi: 10.1083/jcb.112.6.1083.
6
Visualization of centromere proteins CENP-B and CENP-C on a stable dicentric chromosome in cytological spreads.在细胞学涂片的稳定双着丝粒染色体上对着丝粒蛋白CENP - B和CENP - C进行可视化观察。
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7
Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres.着丝粒蛋白A的免疫定位表明,在活跃着丝粒的内着丝粒板处存在独特的核小体结构。
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8
Human CENP-H multimers colocalize with CENP-A and CENP-C at active centromere--kinetochore complexes.人类着丝粒蛋白H多聚体在活跃的着丝粒-动粒复合体处与着丝粒蛋白A和着丝粒蛋白C共定位。
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Microinjection of antibodies to centromere protein CENP-A arrests cells in interphase but does not prevent mitosis.向着丝粒蛋白CENP-A注射抗体进行显微注射会使细胞停滞在间期,但不会阻止有丝分裂。
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10
The centromere protein CENP-B behaves as a microtubule-associated protein.着丝粒蛋白CENP-B表现为一种微管相关蛋白。
Acta Histochem Suppl. 1991;41:37-43.

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High-resolution mapping of centromeric protein association using APEX-chromatin fibers.使用 APEX-染色质纤维进行着丝粒蛋白关联的高分辨率作图。
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A Chemical Proteomics Approach to Reveal Direct Protein-Protein Interactions in Living Cells.一种用于揭示活细胞中直接蛋白质-蛋白质相互作用的化学蛋白质组学方法。
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10
Stepwise unfolding supports a subunit model for vertebrate kinetochores.逐步展开支持脊椎动物动粒的亚基模型。
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本文引用的文献

1
Chromosome walking shows a highly homologous repetitive sequence present in all the centromere regions of fission yeast.染色体步移显示,裂殖酵母的所有着丝粒区域都存在高度同源的重复序列。
EMBO J. 1986 May;5(5):1011-21. doi: 10.1002/j.1460-2075.1986.tb04316.x.
2
Kinetochore structure, duplication, and distribution in mammalian cells: analysis by human autoantibodies from scleroderma patients.哺乳动物细胞中动粒的结构、复制及分布:利用硬皮病患者的人类自身抗体进行分析
J Cell Biol. 1981 Oct;91(1):95-102. doi: 10.1083/jcb.91.1.95.
3
Electron microscope specimen preparation of rat liver chromatin by a modified Miller spreading technique.采用改良的米勒铺展技术制备大鼠肝脏染色质的电子显微镜标本。
Eur J Cell Biol. 1981 Jun;24(2):309-16.
4
Distribution of kinetochore (centromere) antigen in mammalian cell nuclei.动粒(着丝粒)抗原在哺乳动物细胞核中的分布。
J Cell Biol. 1981 Jul;90(1):254-9. doi: 10.1083/jcb.90.1.254.
5
Autoantibody to centromere (kinetochore) in scleroderma sera.硬皮病血清中的着丝粒(动粒)自身抗体。
Proc Natl Acad Sci U S A. 1980 Mar;77(3):1627-31. doi: 10.1073/pnas.77.3.1627.
6
Localization of gold in biological tissue. A photochemical method for light and electronmicroscopy.生物组织中金的定位。一种用于光学显微镜和电子显微镜的光化学方法。
Histochemistry. 1981;71(1):81-8. doi: 10.1007/BF00592572.
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Highly repeated sequences in mammalian genomes.哺乳动物基因组中的高度重复序列。
Int Rev Cytol. 1982;76:67-112. doi: 10.1016/s0074-7696(08)61789-1.
8
Yeast centromere DNA is in a unique and highly ordered structure in chromosomes and small circular minichromosomes.酵母着丝粒DNA在染色体和小型环状微型染色体中呈独特且高度有序的结构。
Cell. 1982 Jun;29(2):305-17. doi: 10.1016/0092-8674(82)90147-7.
9
Silver staining, immunofluorescence, and immunoelectron microscopic localization of nucleolar phosphoproteins B23 and C23.核仁磷蛋白B23和C23的银染、免疫荧光及免疫电子显微镜定位
Chromosoma. 1984;90(2):139-48. doi: 10.1007/BF00292451.
10
The formation, structure, and composition of the mammalian kinetochore and kinetochore fiber.哺乳动物动粒和动粒纤维的形成、结构及组成。
Int Rev Cytol. 1982;79:1-58. doi: 10.1016/s0074-7696(08)61672-1.

着丝粒蛋白B:一种主要的人类着丝粒蛋白,位于动粒下方。

CENP-B: a major human centromere protein located beneath the kinetochore.

作者信息

Cooke C A, Bernat R L, Earnshaw W C

机构信息

Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

J Cell Biol. 1990 May;110(5):1475-88. doi: 10.1083/jcb.110.5.1475.

DOI:10.1083/jcb.110.5.1475
PMID:2335558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2200172/
Abstract

The family of three structurally related autoantigens CENP-A (17 kD), CENP-B (80 kD), and CENP-C (140 kD) are the best characterized components of the human centromere, and they have been widely assumed to be components of the kinetochore. Kinetochore components are currently of great interest since this structure, which has long been known to be the site of microtubule attachment to the chromosome, is now believed to be a site of force production for anaphase chromosome movement. In the present study we have mapped the distribution of CENP-B in mitotic chromosomes by immunoelectron microscopy using two monospecific polyclonal antibodies together with a newly developed series of ultra-small 1-nm colloidal gold probes. We were surprised to find that greater than 95% of CENP-B is distributed throughout the centromeric heterochromatin beneath the kinetochore. This strongly supports other emerging evidence that CENP-B is specifically associated with alpha-satellite heterochromatin. Although in certain instances CENP-B can be seen to be concentrated immediately adjacent to the lower surface of the kinetochore, the outer plate remains virtually unlabeled. Similar analysis with a human autoimmune serum that recognizes all three CENP antigens reveals an additional unsuspected feature of kinetochore structure. In addition to recognizing antigens in the centromeric heterochromatin, the autoantiserum recognizes a concentration of antigens lateral to the kinetochore. This difference in staining pattern may reflect the presence of a "collar" of chromatin rich in CENP-C and/or CENP-A encircling the kinetochore plates.

摘要

三种结构相关的自身抗原CENP-A(17kD)、CENP-B(80kD)和CENP-C(140kD)是人类着丝粒中特征最明显的成分,人们普遍认为它们是动粒的组成部分。动粒成分目前备受关注,因为长期以来已知该结构是微管附着于染色体的位点,现在人们认为它是后期染色体运动的力产生位点。在本研究中,我们使用两种单特异性多克隆抗体以及新开发的一系列超小的1纳米胶体金探针,通过免疫电子显微镜绘制了有丝分裂染色体中CENP-B的分布。我们惊讶地发现,超过95%的CENP-B分布在动粒下方的着丝粒异染色质中。这有力地支持了其他新出现的证据,即CENP-B与α卫星异染色质特异性相关。尽管在某些情况下可以看到CENP-B紧邻动粒的下表面聚集,但动粒的外板几乎没有标记。用识别所有三种CENP抗原的人类自身免疫血清进行的类似分析揭示了动粒结构的另一个意外特征。除了识别着丝粒异染色质中的抗原外,自身抗血清还识别动粒侧面的抗原聚集。这种染色模式的差异可能反映了围绕动粒板的富含CENP-C和/或CENP-A的染色质“环”的存在。