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鸡肝染色质上卵黄蛋白原序列的体外转录

In vitro transcription of vitellogenin sequences on chick liver chromatin.

作者信息

Dierks-Ventling C

出版信息

Nucleic Acids Res. 1978 Oct;5(10):3929-43. doi: 10.1093/nar/5.10.3929.

DOI:10.1093/nar/5.10.3929
PMID:724504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC342720/
Abstract

The in vitro transcription of chick liver chromatin before and after estrogen treatment was studied. Transcription was by endogenous as well as homologous exogenous RNA polymerase II and the products were analyzed for size and specific vitellogenin sequences. Quantitatively more RNA was synthesized from chromatin of 24 h estrogen-treated (E 24) chicks than from that of untreated chicks. In either case the size of transcribed RNA ranged from 5S to larger than 28S and most was between 5S and 18S. When a fraction enriched in estrogen receptor (E-Rec) complex was added to chromatin from untreated chicks, a dramatic shift of the RNA transcribed into heavier regions occurred. Analysis of RNA transcripts by hybridization to cDNAvit showed an equal number of sequences transcribed from E 24 chromatin and control; however, 13 times more specific sequences were transcribed in the presence of E-Rec complex. The results indicate the E-Rec complex exerts a regulatory function in the specific transcription of the vitellogenin gene.

摘要

研究了雌激素处理前后鸡肝脏染色质的体外转录情况。转录由内源性以及同源外源性RNA聚合酶II进行,并且对产物的大小和特异性卵黄生成素序列进行了分析。从经24小时雌激素处理(E24)的雏鸡染色质中合成的RNA在数量上比未经处理的雏鸡更多。在任何一种情况下,转录的RNA大小范围从5S到大于28S,大多数在5S和18S之间。当将富含雌激素受体(E-Rec)复合物的组分添加到未经处理的雏鸡的染色质中时,转录的RNA会发生显著的向较重区域的转移。通过与cDNAvit杂交对RNA转录本进行分析表明,从E24染色质和对照中转录的序列数量相等;然而,在E-Rec复合物存在的情况下,转录的特异性序列多出13倍。结果表明E-Rec复合物在卵黄生成素基因的特异性转录中发挥调节功能。

相似文献

1
In vitro transcription of vitellogenin sequences on chick liver chromatin.鸡肝染色质上卵黄蛋白原序列的体外转录
Nucleic Acids Res. 1978 Oct;5(10):3929-43. doi: 10.1093/nar/5.10.3929.
2
Distribution of estradiol receptor and vitellogenin gene in chick liver chromatin fractions.雌二醇受体和卵黄蛋白原基因在鸡肝脏染色质组分中的分布。
Nucleic Acids Res. 1979 Dec 11;7(7):2031-44. doi: 10.1093/nar/7.7.2031.
3
Stimulation of RNA polymerase I and II activities by 17 beta -estradiol receptor on chick liver chromatin.17β-雌二醇受体对鸡肝染色质中RNA聚合酶I和II活性的刺激作用。
Nucleic Acids Res. 1977 Feb;4(2):381-95. doi: 10.1093/nar/4.2.381.
4
Steroid hormone regulation of vitellogenin gene expression.类固醇激素对卵黄蛋白原基因表达的调控。
CRC Crit Rev Biochem. 1982 Mar;12(3):187-203. doi: 10.3109/10409238209108706.
5
Specific modulation of the transcription of cloned avian vitellogenin II gene by estradiol-receptor complex in vitro.体外雌二醇-受体复合物对克隆的禽卵黄生成素II基因转录的特异性调控
Proc Natl Acad Sci U S A. 1985 Feb;82(4):988-91. doi: 10.1073/pnas.82.4.988.
6
Specific transcription in chicken liver chromatin by endogenous RNA polymerase II. Comparison of an estrogen-inducible gene with a constitutively expressed gene.鸡肝染色质中内源性RNA聚合酶II的特异性转录。雌激素诱导基因与组成型表达基因的比较。
J Biol Chem. 1979 Oct 10;254(19):9860-6.
7
Activation of vitellogenin gene transcription is a direct response to estrogen in Xenopus laevis liver.在非洲爪蟾肝脏中,卵黄蛋白原基因转录的激活是对雌激素的直接反应。
Nucleic Acids Res. 1982 Dec 20;10(24):8273-84. doi: 10.1093/nar/10.24.8273.
8
[Characterization of specific receptors for estradiol, induction of vitellogenin and its mRNA in the liver of rainbow trout (Salmo gairdnerii)].[虹鳟(Salmo gairdnerii)肝脏中雌二醇特异性受体的表征、卵黄蛋白原及其mRNA的诱导]
Biochimie. 1985 Feb;67(2):215-25. doi: 10.1016/s0300-9084(85)80050-x.
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Regulation by estrogen receptor of vitellogenin gene transcription in Xenopus hepatocyte cultures.非洲爪蟾肝细胞培养物中雌激素受体对卵黄蛋白原基因转录的调控
Mol Cell Endocrinol. 1984 Dec;38(2-3):151-61. doi: 10.1016/0303-7207(84)90113-8.
10
Characterization of chick liver chromatin and analysis of its in vitro transcription products.鸡肝脏染色质的表征及其体外转录产物的分析。
Nucleic Acids Res. 1978 Jul;5(7):2643-56. doi: 10.1093/nar/5.7.2643.

本文引用的文献

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Further studies of a thymus nucleohistone-associated protease.胸腺核组蛋白相关蛋白酶的进一步研究。
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Transcription of ribonucleic acid in isolated mouse myeloma nuclei.分离的小鼠骨髓瘤细胞核中核糖核酸的转录
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Nucleic Acids Res. 1977 Feb;4(2):381-95. doi: 10.1093/nar/4.2.381.
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Ovalbumin gene is split in chicken DNA.卵清蛋白基因在鸡的DNA中是断裂的。
Nature. 1977 Nov 24;270(5635):314-9. doi: 10.1038/270314a0.