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[(3H)氢化可的松在大鼠肝细胞核中的定位]

[Localization of (3H)hydrocortisone in rat liver nuclei].

作者信息

Smirnov V G, Kir'ianov G I, Vaniushin B F

出版信息

Biokhimiia. 1978 Oct;43(10):1845-53.

PMID:719054
Abstract

The content of hydrocortisone in rat liver nuclei reaches its maximum in 1 hour after its intravenous injection and remains stable for another hour. In three hours after introduction it falls to the initial level (15 min after the injection of [3H]hydrocortisone). The accumulation of the hormone in nuclei completely coincides with kinetics of reversible DNA supermethylation and correlates with the induction of transcription. No free [3H]hydrocortisone was found in nuclei, in isolated nuclei it is found in the fraction of nuclear membranes, nucleoplasma, nucleolus and chromatin. Specific radioactivity of [3H]hydrocortisone (d. p. m. per 1 mg of DNA) in active chromatin is 10--50-fold as high as in condensed chromatin and is 10--15-fold as high as in nucleolus. It is suggested that there are at least two types of binding hormonereceptor complexes with chromatin. The initial binding of these complexes with condensed chromatin may result in its structural rearrangement (euchromatization), in the appearance of more specific secondary sites for binding hormone-receptor complexes with chromatin DNA, and also in the appearance of methylation and transcription initiation sites in DNA.

摘要

大鼠肝细胞核中氢化可的松的含量在静脉注射后1小时达到最高值,并在接下来的1小时内保持稳定。注射后3小时,其含量降至初始水平(注射[3H]氢化可的松15分钟后)。激素在细胞核中的积累与可逆性DNA超甲基化的动力学完全一致,并与转录诱导相关。在细胞核中未发现游离的[3H]氢化可的松,在分离的细胞核中,它存在于核膜、核质、核仁和染色质部分。活性染色质中[3H]氢化可的松的比放射性(每1毫克DNA的每分钟衰变数)比浓缩染色质高10至50倍,比核仁高10至15倍。有人提出,至少存在两种与染色质结合的激素受体复合物类型。这些复合物与浓缩染色质的初始结合可能导致其结构重排(常染色质化),出现更多与染色质DNA结合激素受体复合物的特异性二级位点,以及DNA中甲基化和转录起始位点的出现。

相似文献

1
[Localization of (3H)hydrocortisone in rat liver nuclei].[(3H)氢化可的松在大鼠肝细胞核中的定位]
Biokhimiia. 1978 Oct;43(10):1845-53.
2
[Binding of glucocorticoid-receptor complexes with the acceptor zones of nuclei and effect of glucocorticoids on RNA synthesis in hormone-sensitive and hormone-resistant cell populations].[糖皮质激素受体复合物与细胞核受体区域的结合以及糖皮质激素对激素敏感和激素抵抗细胞群体中RNA合成的影响]
Biokhimiia. 1982 Feb;47(2):206-15.
3
[DNA methylation and interaction with glucocorticoid receptor complexes in the rat liver].
Biokhimiia. 1987 May;52(5):870-7.
4
[Methylation and degradation of chromatin DNA in isolated rat liver cell nuclei].
Biokhimiia. 1979 Jun;44(6):1058-67.
5
[Changes in the state of hormone-receptor complexes which contain specific binding sites of rat liver chromatin particles as affected by cortisol].
Biokhimiia. 1984 Oct;49(10):1634-9.
6
[Participation of chromatin proteins in the binding of glucocorticoid receptor complexes by the cell nucleus].[染色质蛋白参与细胞核对糖皮质激素受体复合物的结合]
Nauchnye Doki Vyss Shkoly Biol Nauki. 1984(4):22-6.
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Actinomycin D binding in vitro: active chromatin preferred.放线菌素D的体外结合:优先结合活性染色质。
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[Hydrocortisone-receptor complex binding with various nonhistone protein groups].[氢化可的松 - 受体复合物与各种非组蛋白蛋白基团的结合]
Vopr Med Khim. 1980 Sep-Oct;26(5):656-9.
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[Age-related decrease of the binding of isolated rat liver and brain nuclei with glucocorticoid-receptor complexes].[大鼠离体肝脏和脑细胞核与糖皮质激素受体复合物结合的年龄相关性降低]
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[Transition of the specific binding sites of glucocorticoid receptor complexes from the fraction of potentially active DNA into the fraction of transcriptionally active DNA under cortisol induction in rat liver cells].[在大鼠肝细胞中皮质醇诱导下糖皮质激素受体复合物特异性结合位点从潜在活性DNA组分向转录活性DNA组分的转变]
Dokl Akad Nauk SSSR. 1983;272(3):739-41.