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Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte.非洲爪蟾卵母细胞减数分裂成熟过程中,非洲爪蟾hsp70启动子上调节性核蛋白复合物的重塑。
EMBO J. 1997 Jul 16;16(14):4361-73. doi: 10.1093/emboj/16.14.4361.
2
The heat shock response in Xenopus oocytes, embryos, and somatic cells: a regulatory role for chromatin.非洲爪蟾卵母细胞、胚胎及体细胞中的热休克反应:染色质的调控作用
Dev Biol. 1995 Jul;170(1):62-74. doi: 10.1006/dbio.1995.1195.
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本文引用的文献

1
ON THE RNA SYNTHESIZED DURING THE LAMPBRUSH PHASE OF AMPHIBIAN OOEGENESIS.关于两栖类卵子发生灯刷期合成的RNA
Proc Natl Acad Sci U S A. 1964 Aug;52(2):501-8. doi: 10.1073/pnas.52.2.501.
2
VARIATIONS IN THE SYNTHESIS OF STABLE RNA'S DURING OOGENESIS AND DEVELOPMENT OF XENOPUS LAEVIS.非洲爪蟾卵子发生和发育过程中稳定RNA合成的变化
J Mol Biol. 1964 May;8:688-95. doi: 10.1016/s0022-2836(64)80117-0.
3
Cytoplasmic regulation of 5S RNA genes in nuclear-transplant embryos.核移植胚胎中5S RNA基因的细胞质调控
EMBO J. 1983;2(9):1613-9. doi: 10.1002/j.1460-2075.1983.tb01632.x.
4
Determinants of chromatin disruption and transcriptional regulation instigated by the thyroid hormone receptor: hormone-regulated chromatin disruption is not sufficient for transcriptional activation.甲状腺激素受体引发的染色质破坏和转录调控的决定因素:激素调节的染色质破坏不足以实现转录激活。
EMBO J. 1997 Jun 2;16(11):3158-71. doi: 10.1093/emboj/16.11.3158.
5
RSC, an essential, abundant chromatin-remodeling complex.RSC,一种必需的、丰富的染色质重塑复合体。
Cell. 1996 Dec 27;87(7):1249-60. doi: 10.1016/s0092-8674(00)81820-6.
6
Mitotic regulation of TFIID: inhibition of activator-dependent transcription and changes in subcellular localization.
Genes Dev. 1996 Oct 1;10(19):2389-400. doi: 10.1101/gad.10.19.2389.
7
The regulation of euchromatin and heterochromatin by histones in yeast.酵母中组蛋白对常染色质和异染色质的调控。
J Cell Sci Suppl. 1995;19:29-36. doi: 10.1242/jcs.1995.supplement_19.4.
8
Hyperphosphorylation of nucleoplasmin facilitates Xenopus sperm decondensation at fertilization.核质蛋白的过度磷酸化有助于非洲爪蟾精子在受精时解聚。
J Biol Chem. 1996 Mar 29;271(13):7253-6. doi: 10.1074/jbc.271.13.7253.
9
An ATP-dependent inhibitor of TBP binding to DNA.一种依赖ATP的TBP与DNA结合的抑制剂。
Genes Dev. 1993 May;7(5):844-56. doi: 10.1101/gad.7.5.844.
10
Nuclear assembly, structure, and function: the use of Xenopus in vitro systems.细胞核组装、结构与功能:非洲爪蟾体外系统的应用
Exp Cell Res. 1993 Mar;205(1):1-15. doi: 10.1006/excr.1993.1051.

非洲爪蟾卵母细胞减数分裂成熟过程中,非洲爪蟾hsp70启动子上调节性核蛋白复合物的重塑。

Remodeling of regulatory nucleoprotein complexes on the Xenopus hsp70 promoter during meiotic maturation of the Xenopus oocyte.

作者信息

Landsberger N, Wolffe A P

机构信息

Laboratory of Molecular Embryology, National Institute of Child Health and Human Development, NIH, Bethesda, MD 20892-5431, USA.

出版信息

EMBO J. 1997 Jul 16;16(14):4361-73. doi: 10.1093/emboj/16.14.4361.

DOI:10.1093/emboj/16.14.4361
PMID:9250680
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1170062/
Abstract

Transcriptional repression occurs during meiotic maturation of Xenopus oocytes. Injection of a DNA template containing an hsp70 promoter into Xenopus oocytes, followed by progesterone-induced maturation has been used to demonstrate a dynamic competition between the assembly of transcription factor-containing nucleoprotein complexes and repressive nucleosomal arrays during the maturation process. In particular, it is shown that increased levels of injected heat shock protein, the transcriptional activator Gal4-VP16 or the DNA template itself all lead to reduced repression of transcription on maturation. Conversely, injection of additional histone increases repression. Repression of transcription is shown to be accompanied by the formation of a more regular array of nucleosomes and by an increase in the efficiency of nucleosome assembly on the injected plasmid. Meiotic maturation is therefore accompanied by replacement of transcription factor complexes by a repressive chromatin environment.

摘要

转录抑制发生在非洲爪蟾卵母细胞的减数分裂成熟过程中。将含有热休克蛋白70(hsp70)启动子的DNA模板注入非洲爪蟾卵母细胞,随后用孕酮诱导成熟,以此来证明在成熟过程中含转录因子的核蛋白复合物组装与抑制性核小体阵列之间存在动态竞争。具体而言,研究表明,注射的热休克蛋白、转录激活因子Gal4-VP16或DNA模板本身水平的增加,都会导致成熟过程中转录抑制的降低。相反,额外注射组蛋白会增强抑制作用。转录抑制伴随着更规则的核小体阵列的形成以及注射质粒上核小体组装效率的提高。因此,减数分裂成熟伴随着转录因子复合物被抑制性染色质环境所取代。