• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

染色质中组蛋白H1的交联

Cross-linking of histone H1 in chromatin.

作者信息

Thomas J O, Khabaza A J

出版信息

Eur J Biochem. 1980 Dec;112(3):501-11. doi: 10.1111/j.1432-1033.1980.tb06113.x.

DOI:10.1111/j.1432-1033.1980.tb06113.x
PMID:7460934
Abstract

Arrays of neighbouring histone H1 molecules are present in rat liver chromatin, and can be cross-linked to each other by bisimidoesters. The product, poly(H1), can be extracted from cross-linked chromatin in high yield with 5% perchloric acid and thus distinguished from cross-linked oligomers of the core histones. On analysis in dodecyl sulphate/polyacrylamide gels poly(H1) gives a striking pattern of alternating strong and weak bands which have been shown, by the use of cleavable cross-linked reagents and two-dimensional gel electrophoresis, to arise respectively from H1 homopolymers and H1 polymers linked to the nucleosome core histones. H1-H1 proximities as measured by cross-linking exist both at low ionic strength where the nucleosome filament is extended, and at higher ionic strengths at which it is folded into a 30-nm-diameter fibre, probably in the form of a solenoid, although some additional H1-H1 contacts seem to occur in the folded form. A similar pattern of H1-H1 cross-linking is observed for nucleosome oligomers too short to form a complete turn of a solenoid. The lack of any strong dependence of the H1 cross-linking pattern on ionic strength, and the results for short oligomers, suggest that in a solenoid the major H1-H1 interactions are lateral (i.e. they occur between neighbouring nucleosomes along a turn) although additional vertical contacts (between successive turns) are not excluded. For a short nucleosome oligomer containing n nucleosomes, the number of H1 molecules that may be cross-linked into an array at low ionic strength (approximately 15 mM) is n, consistent with the presence of one H1 per nucleosome. H1-H1 cross-linking occurs only within the chromatin framework; when cross-linking is carried out in 0.5 M NaCl so that H1 is dissociated from chromatin, no poly(H1) is formed. When H1 which has been dissociated in 0.5 M NaCl is allowed to reassociate by gradual lowering of the ionic strength, the poly(H1) is identical with that in native chromatin, suggesting faithful rebinding of H1 molecules. H1-H1 proximities do not seem to be mediated by the presence of bound high-mobility-group non-histone proteins because the poly(H1) pattern persists when cross-linking is carried out at 365 mM ionic strength, when these high-mobility-group proteins are dissociated from chromatin. The H1 cross-linking pattern described here could prove to be a useful assay for the native arrangement of H1 molecules in reconstituted chromatin and for changes in H1-H1 contacts that might result from cell-cycle modifications (e.g phosphorylation) of H1. It may not prove a good assay for higher-order structure because of the relative insensitivity to ionic strength of the poly(H1) pattern as studied here. A detailed analysis will be necessary to determine whether there are any subtle differences in the interactions between H1 molecules in the folded and extended nucleosome filament.

摘要

相邻的组蛋白H1分子阵列存在于大鼠肝脏染色质中,并且可以通过双亚胺酯彼此交联。产物聚(H1)可以用5%的高氯酸从交联染色质中高产率提取出来,从而与核心组蛋白的交联寡聚体区分开来。在十二烷基硫酸钠/聚丙烯酰胺凝胶中分析时,聚(H1)呈现出明显的强弱交替条带模式,通过使用可裂解的交联试剂和二维凝胶电泳表明,这些条带分别来自H1同聚物和与核小体核心组蛋白相连的H1聚合物。通过交联测量的H1-H1邻近性既存在于核小体细丝伸展的低离子强度下,也存在于其折叠成直径30nm纤维(可能呈螺线管形式)的较高离子强度下,尽管在折叠形式中似乎还会发生一些额外的H1-H1接触。对于太短而无法形成完整一圈螺线管的核小体寡聚体,也观察到类似的H1-H1交联模式。H1交联模式对离子强度缺乏强烈依赖性以及短寡聚体的结果表明,在螺线管中,主要的H1-H1相互作用是横向的(即它们发生在沿一圈的相邻核小体之间),尽管不排除额外的垂直接触(在连续几圈之间)。对于含有n个核小体的短核小体寡聚体,在低离子强度(约15mM)下可能交联成阵列的H1分子数量为n,这与每个核小体存在一个H1一致。H1-H1交联仅发生在染色质框架内;当在0.5M NaCl中进行交联以使H1从染色质上解离时,不会形成聚(H1)。当在0.5M NaCl中解离的H1通过逐渐降低离子强度而重新结合时,聚(H1)与天然染色质中的聚(H1)相同,这表明H1分子能忠实重新结合。H1-H1邻近性似乎不是由结合的高迁移率族非组蛋白的存在介导的,因为当在365mM离子强度下进行交联时,这些高迁移率族蛋白从染色质上解离,而聚(H1)模式仍然存在。这里描述的H​1交联模式可能被证明是一种有用的检测方法,用于检测重组染色质中H1分子的天然排列以及可能由H1的细胞周期修饰(如磷酸化)导致的H​1-H1接触变化。由于这里研究的聚(H1)模式对离子强度相对不敏感,它可能不是检测高阶结构的好方法。需要进行详细分析以确定在折叠和伸展的核小体细丝中H1分子之间的相互作用是否存在任何细微差异。

相似文献

1
Cross-linking of histone H1 in chromatin.染色质中组蛋白H1的交联
Eur J Biochem. 1980 Dec;112(3):501-11. doi: 10.1111/j.1432-1033.1980.tb06113.x.
2
The higher order structure of chromatin and histone H1.染色质的高级结构与组蛋白H1
J Cell Sci Suppl. 1984;1:1-20. doi: 10.1242/jcs.1984.supplement_1.1.
3
Identification of suberimidate cross-linking sites of four histone sequences in H1-depleted chromatin. Histone arrangement in nucleosome core.H1缺失染色质中四种组蛋白序列的亚胺化交联位点鉴定。核小体核心中的组蛋白排列。
J Biochem. 1979 Dec;86(6):1659-70. doi: 10.1093/oxfordjournals.jbchem.a132686.
4
Histone crosslinking patterns indicate dynamic binding of histone H1 in chromatin.
Biochim Biophys Acta. 1985 Mar 20;824(3):185-93. doi: 10.1016/0167-4781(85)90047-8.
5
Involvement of histone H1 in the organization of the nucleosome and of the salt-dependent superstructures of chromatin.组蛋白H1参与核小体的组装以及染色质盐依赖性超结构的形成。
J Cell Biol. 1979 Nov;83(2 Pt 1):403-27. doi: 10.1083/jcb.83.2.403.
6
Conformation of nucleosome core particles and chromatin in high salt concentration.高盐浓度下核小体核心颗粒与染色质的构象
Biochemistry. 1980 Sep 2;19(18):4327-31. doi: 10.1021/bi00559a028.
7
The arrangement of H5 molecules in extended and condensed chicken erythrocyte chromatin.H5分子在伸展和浓缩的鸡红细胞染色质中的排列。
EMBO J. 1985 Dec 16;4(13A):3455-62. doi: 10.1002/j.1460-2075.1985.tb04104.x.
8
Studies on protein organization of nucleosomes using cross-linking.利用交联技术对核小体蛋白质组织进行的研究。
Mol Biol Rep. 1981 Aug 14;7(4):209-16. doi: 10.1007/BF00805754.
9
Fractionation of nucleosomes by salt elution from micrococcal nuclease-digested nuclei.通过从微球菌核酸酶消化的细胞核中进行盐洗脱来分离核小体。
J Cell Biol. 1978 Oct;79(1):97-109. doi: 10.1083/jcb.79.1.97.
10
A nonamer of histones in chromatin.染色质中的组蛋白九聚体。
J Biol Chem. 1980 May 25;255(10):4511-5.

引用本文的文献

1
Structural basis for linker histone H5-nucleosome binding and chromatin fiber compaction.连接组蛋白 H5 与核小体结合及染色质纤维紧缩的结构基础。
Cell Res. 2024 Oct;34(10):707-724. doi: 10.1038/s41422-024-01009-z. Epub 2024 Aug 5.
2
Complex of linker histone H5 with the nucleosome and its implications for chromatin packing.连接组蛋白H5与核小体的复合体及其对染色质组装的影响。
Proc Natl Acad Sci U S A. 2006 May 30;103(22):8384-9. doi: 10.1073/pnas.0508951103. Epub 2006 May 22.
3
Sir2p exists in two nucleosome-binding complexes with distinct deacetylase activities.
Sir2p存在于两种具有不同脱乙酰酶活性的核小体结合复合物中。
EMBO J. 2001 Aug 15;20(16):4522-35. doi: 10.1093/emboj/20.16.4522.
4
A model for chromatin opening: stimulation of topoisomerase II and restriction enzyme cleavage of chromatin by distamycin.一种染色质开放模型:偏端霉素对拓扑异构酶II的刺激作用及对染色质限制性内切酶切割的影响
EMBO J. 1993 Jan;12(1):115-26. doi: 10.1002/j.1460-2075.1993.tb05637.x.
5
Coexistence of two chromatin structures in sperm nuclei of the bivalve mollusc Protothaca thaca.双壳贝类软体动物Protothaca thaca精子细胞核中两种染色质结构的共存。
Mol Cell Biochem. 1993 Aug 11;125(1):87-95. doi: 10.1007/BF00926838.
6
The effect of histone H1 and DNA methylation on transcription.组蛋白H1和DNA甲基化对转录的影响。
Biochem J. 1995 Feb 1;305 ( Pt 3)(Pt 3):791-8. doi: 10.1042/bj3050791.
7
Participation of core histone "tails" in the stabilization of the chromatin solenoid.核心组蛋白“尾巴”在染色质螺线管稳定中的作用。
J Cell Biol. 1982 May;93(2):285-97. doi: 10.1083/jcb.93.2.285.
8
The higher-order structure of chromatin: evidence for a helical ribbon arrangement.染色质的高阶结构:螺旋带排列的证据。
J Cell Biol. 1984 Jul;99(1 Pt 1):42-52. doi: 10.1083/jcb.99.1.42.
9
Cross-linking of histones with dimethyl 3,3'-dithiobispropionimidate. Interference by a one-end reaction modifying histones at lysine amino groups.组蛋白与二甲基3,3'-二硫代双丙亚氨酸酯的交联。一端反应修饰赖氨酸氨基处组蛋白所产生的干扰。
Biochem J. 1984 Dec 15;224(3):1019-22. doi: 10.1042/bj2241019.
10
The arrangement of H5 molecules in extended and condensed chicken erythrocyte chromatin.H5分子在伸展和浓缩的鸡红细胞染色质中的排列。
EMBO J. 1985 Dec 16;4(13A):3455-62. doi: 10.1002/j.1460-2075.1985.tb04104.x.