• 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

海胆组蛋白基因在HeLa细胞中的转录

Transcription of sea urchin histone genes in HeLa cells.

作者信息

Bendig M M, Hentschel C C

出版信息

Nucleic Acids Res. 1983 Apr 25;11(8):2337-46. doi: 10.1093/nar/11.8.2337.

DOI:10.1093/nar/11.8.2337
PMID:6304648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC325888/
Abstract

HeLa cells were transfected with recombinant DNAs containing the embryonic histone gene repeat of P.miliaris (h22) inserted in either orientation into a pBR-SV40 vector. After 2 to 3 days cytoplasmic RNA was analyzed for authentic sea urchin histone gene transcripts. The correct 5' termini of all five histone genes were detected, three (H2B, H2A and H3) at relatively high levels. In contrast, termination was largely aberrant with the correct 3' terminus of only the H2B mRNA found in significant amounts. The levels of histone gene transcription were dependent on the presence, but not the orientation, of SV40 DNA in the recombinant plasmid. The efficiency of initiation of transcription of the individual sea urchin histone genes in HeLa cells was very similar to that previously observed in Xenopus oocytes. The termination pattern, however, was quite different in that oocytes, all but the H3 gene terminate efficiently. The idiosyncrasies in termination efficiencies for these two heterologous transcription systems may reflect the presence of termination factors which are relatively species or even tissue specific and only some of which recognize the sea urchin "terminators" correctly.

摘要

将含有插入到pBR - SV40载体中的粟酒裂殖酵母胚胎组蛋白基因重复序列(h22)的重组DNA以任一方向转染HeLa细胞。2至3天后,分析细胞质RNA中的真实海胆组蛋白基因转录本。检测到所有五个组蛋白基因的正确5'末端,其中三个(H2B、H2A和H3)的水平相对较高。相比之下,终止大多异常,仅在大量存在的H2B mRNA中发现了正确的3'末端。组蛋白基因转录水平取决于重组质粒中SV40 DNA的存在,但不取决于其方向。HeLa细胞中单个海胆组蛋白基因的转录起始效率与先前在非洲爪蟾卵母细胞中观察到的非常相似。然而,终止模式却大不相同,在卵母细胞中,除了H3基因外,所有基因都能有效终止。这两个异源转录系统在终止效率上的特性可能反映了终止因子的存在,这些终止因子相对具有物种甚至组织特异性,并且只有其中一些能正确识别海胆“终止子”。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/11d49e8af7e1/nar00353-0113-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/e019f9e0045b/nar00353-0111-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/5dbde6f2a0d3/nar00353-0112-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/11d49e8af7e1/nar00353-0113-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/e019f9e0045b/nar00353-0111-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/5dbde6f2a0d3/nar00353-0112-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d24/325888/11d49e8af7e1/nar00353-0113-a.jpg

相似文献

1
Transcription of sea urchin histone genes in HeLa cells.海胆组蛋白基因在HeLa细胞中的转录
Nucleic Acids Res. 1983 Apr 25;11(8):2337-46. doi: 10.1093/nar/11.8.2337.
2
Generation of authentic 3' termini of an H2A mRNA in vivo is dependent on a short inverted DNA repeat and on spacer sequences.H2A信使核糖核酸(mRNA)在体内真实3'末端的产生取决于一个短的反向DNA重复序列和间隔序列。
Cell. 1982 Apr;28(4):739-45. doi: 10.1016/0092-8674(82)90053-8.
3
The synthesis of authentic sea urchin transcriptional and translational products by sea urchin histone genes injected into Xenopus laevis oocytes.将海胆组蛋白基因注射到非洲爪蟾卵母细胞中后,其合成出真实的海胆转录和翻译产物。
Dev Biol. 1980 Mar;75(1):13-25. doi: 10.1016/0012-1606(80)90140-2.
4
Histone gene switch in the sea urchin embryo. Identification of late embryonic histone messenger ribonucleic acids and the control of their synthesis.海胆胚胎中的组蛋白基因转换。晚期胚胎组蛋白信使核糖核酸的鉴定及其合成调控。
Biochemistry. 1979 Jun 26;18(13):2707-16. doi: 10.1021/bi00580a004.
5
Subcloning of the histone DNA sequences of phage lambda Sam 7 h 22 in plasmid pBR 322.噬菌体λ Sam 7 h 22的组蛋白DNA序列在质粒pBR 322中的亚克隆。
Z Naturforsch C Biosci. 1980 Sep-Oct;35(9-10):733-40. doi: 10.1515/znc-1980-9-1014.
6
Nonallelic histone gene clusters of individual sea urchins (Lytechinus pictus): polarity and gene organization.个体海胆(紫球海胆)的非等位组蛋白基因簇:极性与基因组织
Cell. 1979 Nov;18(3):843-53. doi: 10.1016/0092-8674(79)90136-3.
7
The inability of the Psammechinus miliaris H3 RNA to be processed in the Xenopus oocyte is associated with sequences distinct from those highly conserved amongst sea urchin histone RNAs.米氏刻肋海胆(Psammechinus miliaris)的H3 RNA在非洲爪蟾卵母细胞中无法进行加工,这与海胆组蛋白RNA中高度保守的序列不同的序列有关。
Nucleic Acids Res. 1987 Oct 26;15(20):8305-17. doi: 10.1093/nar/15.20.8305.
8
Tripartite sequences within and 3' to the sea urchin H2A histone gene display properties associated with a transcriptional termination process.海胆H2A组蛋白基因内部及其3'端的三联体序列表现出与转录终止过程相关的特性。
Mol Cell Biol. 1986 Nov;6(11):4008-18. doi: 10.1128/mcb.6.11.4008-4018.1986.
9
Transcription of sea urchin histone genes in Escherichia coli.海胆组蛋白基因在大肠杆菌中的转录
Nucleic Acids Res. 1981 Aug 25;9(16):3889-906. doi: 10.1093/nar/9.16.3889.
10
Ubiquitous and gene-specific regulatory 5' sequences in a sea urchin histone DNA clone coding for histone protein variants.一个编码组蛋白变体的海胆组蛋白DNA克隆中普遍存在的和基因特异性的调控5'序列。
Nucleic Acids Res. 1980 Mar 11;8(5):957-77. doi: 10.1093/nar/8.5.957.

引用本文的文献

1
The primary structure and expression of four cloned human histone genes.四个克隆的人类组蛋白基因的一级结构与表达
Nucleic Acids Res. 1983 Nov 11;11(21):7409-25. doi: 10.1093/nar/11.21.7409.
2
Attenuation in SV40 as a mechanism of transcription-termination by RNA polymerase B.SV40中的衰减作为RNA聚合酶B转录终止的一种机制。
Nucleic Acids Res. 1984 Feb 10;12(3):1401-14. doi: 10.1093/nar/12.3.1401.
3
Transcription of a cloned rainbow trout protamine gene is accurately initiated following transfection into HeLa cells but the majority of the transcripts fail to polyadenylate at the correct site.

本文引用的文献

1
Linear DNA does not form chromatin containing regularly spaced nucleosomes.线性DNA不会形成含有规则间隔核小体的染色质。
Mol Cell Biol. 1982 Dec;2(12):1608-18. doi: 10.1128/mcb.2.12.1608-1618.1982.
2
Transcriptional fidelity of histone genes injected into Xenopus oocyte nuclei.注射到非洲爪蟾卵母细胞核中的组蛋白基因的转录保真度。
Nature. 1980 Nov 6;288(5786):100-2. doi: 10.1038/288100a0.
3
Sea urchin histone mRNA termini are located in gene regions downstream from putative regulatory sequences.海胆组蛋白mRNA末端位于假定调控序列下游的基因区域。
克隆的虹鳟鱼鱼精蛋白基因转染到HeLa细胞后转录能准确起始,但大多数转录本未能在正确位点进行多聚腺苷酸化。
Nucleic Acids Res. 1985 Dec 20;13(24):8715-27. doi: 10.1093/nar/13.24.8715.
4
Tripartite sequences within and 3' to the sea urchin H2A histone gene display properties associated with a transcriptional termination process.海胆H2A组蛋白基因内部及其3'端的三联体序列表现出与转录终止过程相关的特性。
Mol Cell Biol. 1986 Nov;6(11):4008-18. doi: 10.1128/mcb.6.11.4008-4018.1986.
5
Polyadenylylation of sea urchin histone RNA sequences in transfected COS cells.转染的COS细胞中海胆组蛋白RNA序列的聚腺苷酸化
Proc Natl Acad Sci U S A. 1985 Feb;82(4):1094-8. doi: 10.1073/pnas.82.4.1094.
Nature. 1980 May 15;285(5761):147-51. doi: 10.1038/285147a0.
4
A split promoter for a eucaryotic tRNA gene.一种真核生物tRNA基因的分裂启动子。
Cell. 1981 May;24(2):573-85. doi: 10.1016/0092-8674(81)90348-2.
5
Persistence and expression of histone genes injected into Xenopus eggs in early development.注入非洲爪蟾卵中的组蛋白基因在早期发育中的持续性和表达
Nature. 1981 Jul 2;292(5818):65-7. doi: 10.1038/292065a0.
6
Bioassay for components regulating eukaryotic gene expression: a chromosomal factor involved in the generation of histone mRNA 3' termini.调节真核基因表达的成分的生物测定:一种参与组蛋白mRNA 3'末端生成的染色体因子。
Proc Natl Acad Sci U S A. 1982 Oct;79(20):6201-4. doi: 10.1073/pnas.79.20.6201.
7
Delimitation of far upstream sequences required for maximal in vitro transcription of an H2A histone gene.H2A组蛋白基因体外最大转录所需的远上游序列的界定
Proc Natl Acad Sci U S A. 1982 Jan;79(2):297-301. doi: 10.1073/pnas.79.2.297.
8
The organization and expression of histone gene families.组蛋白基因家族的组织与表达
Cell. 1981 Aug;25(2):301-13. doi: 10.1016/0092-8674(81)90048-9.
9
Transcription of sea urchin histone genes in Escherichia coli.海胆组蛋白基因在大肠杆菌中的转录
Nucleic Acids Res. 1981 Aug 25;9(16):3889-906. doi: 10.1093/nar/9.16.3889.
10
Generation of authentic 3' termini of an H2A mRNA in vivo is dependent on a short inverted DNA repeat and on spacer sequences.H2A信使核糖核酸(mRNA)在体内真实3'末端的产生取决于一个短的反向DNA重复序列和间隔序列。
Cell. 1982 Apr;28(4):739-45. doi: 10.1016/0092-8674(82)90053-8.