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一个正向转录因子控制两个5S RNA基因的差异表达。

A positive transcription factor controls the differential expression of two 5S RNA genes.

作者信息

Brown D D, Schlissel M S

出版信息

Cell. 1985 Oct;42(3):759-67. doi: 10.1016/0092-8674(85)90272-7.

DOI:10.1016/0092-8674(85)90272-7
PMID:4053184
Abstract

Somatic 5S RNA genes are transcribed preferentially over oocyte 5S RNA genes by 25- to greater than 200-fold when mixtures of cloned genes are injected into cleaving Xenopus embryos. This preference is an order of magnitude greater than that observed in cell-free extracts. Mutations that decrease the binding of the 5S RNA gene-specific transcription factor TFIIIA to the 5S RNA genes' internal control regions are exaggerated when assayed by embryo injection compared to in vitro transcription. Injection of TFIIIA into cleaving embryos greatly increases endogenous oocyte 5S RNA synthesis at midblastula even when DNA replication is inhibited. Much, but not all, of the preference for somatic over oocyte 5S RNA gene transcription in somatic cells can thus be attributed to the concentration of TFIIIA and to differences in binding constants of TFIIIA to the internal control regions of the two types of genes.

摘要

当将克隆基因混合物注射到分裂期的非洲爪蟾胚胎中时,体细胞5S RNA基因的转录优先于卵母细胞5S RNA基因,其转录倍数为25倍至大于200倍。这种偏好比在无细胞提取物中观察到的情况高一个数量级。与体外转录相比,当通过胚胎注射进行检测时,降低5S RNA基因特异性转录因子TFIIIA与5S RNA基因内部控制区结合的突变会被放大。即使在DNA复制受到抑制的情况下,将TFIIIA注射到分裂期胚胎中也会大大增加囊胚中期内源性卵母细胞5S RNA的合成。因此,体细胞中对体细胞5S RNA基因转录而非卵母细胞5S RNA基因转录的偏好,很大程度上(但不是全部)可归因于TFIIIA的浓度以及TFIIIA与这两种基因内部控制区结合常数的差异。

相似文献

1
A positive transcription factor controls the differential expression of two 5S RNA genes.一个正向转录因子控制两个5S RNA基因的差异表达。
Cell. 1985 Oct;42(3):759-67. doi: 10.1016/0092-8674(85)90272-7.
2
TFIIIA binds with equal affinity to somatic and major oocyte 5S RNA genes.TFIIIA与体细胞和主要卵母细胞5S RNA基因以相同的亲和力结合。
Genes Dev. 1988 Feb;2(2):205-14. doi: 10.1101/gad.2.2.205.
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Cell. 1987 Nov 6;51(3):445-53. doi: 10.1016/0092-8674(87)90640-4.
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Transcriptionally inactive oocyte-type 5S RNA genes of Xenopus laevis are complexed with TFIIIA in vitro.非洲爪蟾转录不活跃的卵母细胞型5S RNA基因在体外与TFIIIA复合。
Mol Cell Biol. 1987 Oct;7(10):3503-10. doi: 10.1128/mcb.7.10.3503-3510.1987.
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Internal deletion mutants of Xenopus transcription factor IIIA.非洲爪蟾转录因子IIIA的内部缺失突变体
Nucleic Acids Res. 1989 Dec 11;17(23):9861-70. doi: 10.1093/nar/17.23.9861.
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Sequences preceding the minimal promoter of the Xenopus somatic 5S RNA gene increase binding efficiency for transcription factors.非洲爪蟾体细胞5S RNA基因最小启动子之前的序列可提高转录因子的结合效率。
Nucleic Acids Res. 1989 Nov 25;17(22):9381-94.
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Additional intragenic promoter elements of the Xenopus 5S RNA genes upstream from the TFIIIA-binding site.非洲爪蟾5S RNA基因TFIIIA结合位点上游的额外基因内启动子元件。
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The role of DNA-mediated transfer of TFIIIA in the concerted gyration and differential activation of the Xenopus 5S RNA genes.DNA介导的TFIIIA转移在非洲爪蟾5S RNA基因协同旋转和差异激活中的作用。
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Effect of sequence differences between somatic and oocyte 5S RNA genes on transcriptional efficiency in an oocyte S150 extract.体细胞和卵母细胞5S RNA基因之间的序列差异对卵母细胞S150提取物中转录效率的影响。
Mol Cell Biol. 1988 Nov;8(11):5056-8. doi: 10.1128/mcb.8.11.5056-5058.1988.

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