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以无细胞系统为特征的丝心蛋白基因的组织特异性转录增强

Tissue-specific transcription enhancement of the fibroin gene characterized by cell-free systems.

作者信息

Suzuki Y, Tsuda M, Takiya S, Hirose S, Suzuki E, Kameda M, Ninaki O

出版信息

Proc Natl Acad Sci U S A. 1986 Dec;83(24):9522-6. doi: 10.1073/pnas.83.24.9522.

DOI:10.1073/pnas.83.24.9522
PMID:3467322
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC387172/
Abstract

Six cell-free extracts have been used to characterize the nature of DNA signals and trans-acting factors responsible for the transcription enhancement of the Bombyx mori fibroin gene. The upstream element of the fibroin gene involved in the enhancement can be divided into two regions. The proximal region, -72 to -32, is recognized as a common enhancing signal by all B. mori extracts from the posterior silk gland, the middle silk gland, the ovarian tissue, and an embryonic cell line. It is weakly recognized by an Antheraea silkworm cell line extract but not by a HeLa cell extract. The distal region, -238 to -73, appears to be a tissue-specific enhancing signal that is recognized more effectively by the posterior silk gland extract than by the middle silk gland extract. These observations suggest that the use of these cell-free systems can offer a means for the biochemical characterization of the trans-acting factors involved in the tissue-specific regulation of the fibroin gene.

摘要

六种无细胞提取物已被用于表征负责家蚕丝素基因转录增强的DNA信号和反式作用因子的性质。参与增强作用的丝素基因上游元件可分为两个区域。近端区域,-72至-32,被来自后部丝腺、中部丝腺、卵巢组织和胚胎细胞系的所有家蚕提取物识别为共同的增强信号。它被柞蚕细胞系提取物微弱识别,但不被HeLa细胞提取物识别。远端区域,-238至-73,似乎是一种组织特异性增强信号,后部丝腺提取物比中部丝腺提取物更有效地识别它。这些观察结果表明,使用这些无细胞系统可以为参与丝素基因组织特异性调控的反式作用因子的生化表征提供一种方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/a045d170f5d8/pnas00328-0259-f.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/19343beaf18d/pnas00328-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/6acdba5522fb/pnas00328-0259-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/0fd30b5a4b68/pnas00328-0259-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/4a0465716d72/pnas00328-0259-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/9f32113a4110/pnas00328-0259-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/ea85042adb50/pnas00328-0259-e.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/a045d170f5d8/pnas00328-0259-f.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/19343beaf18d/pnas00328-0258-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/6acdba5522fb/pnas00328-0259-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/0fd30b5a4b68/pnas00328-0259-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/4a0465716d72/pnas00328-0259-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/9f32113a4110/pnas00328-0259-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/ea85042adb50/pnas00328-0259-e.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b935/387172/a045d170f5d8/pnas00328-0259-f.jpg

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本文引用的文献

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Faithful transcription initiation of fibroin gene in a homologous cell-free system reveals an enhancing effect of 5' flanking sequence far upstream.在同源无细胞系统中丝心蛋白基因的忠实转录起始揭示了远上游5'侧翼序列的增强作用。
Cell. 1981 Nov;27(1 Pt 2):175-82. doi: 10.1016/0092-8674(81)90371-8.
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Sequences upstream from the T-A-T-A box are required in vivo and in vitro for efficient transcription from the adenovirus serotype 2 major late promoter.腺病毒2型主要晚期启动子在体内和体外进行有效转录时,需要T-A-T-A框上游的序列。
Proc Natl Acad Sci U S A. 1982 Dec;79(23):7132-6. doi: 10.1073/pnas.79.23.7132.
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Delimitation of far upstream sequences required for maximal in vitro transcription of an H2A histone gene.
家蚕终末分化丝腺中Hox和同源异型结构域蛋白对丝基因的调控
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A juvenile hormone transcription factor Bmdimm-fibroin H chain pathway is involved in the synthesis of silk protein in silkworm, Bombyx mori.一种保幼激素转录因子Bmdimm-丝心蛋白重链途径参与家蚕(Bombyx mori)丝蛋白的合成。
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Basic helix-loop-helix transcription factor Bmsage is involved in regulation of fibroin H-chain gene via interaction with SGF1 in Bombyx mori.Bmsage 是碱性螺旋-环-螺旋转录因子,它通过与 SGF1 互作参与调控家蚕丝素重链基因的表达。
PLoS One. 2014 Apr 16;9(4):e94091. doi: 10.1371/journal.pone.0094091. eCollection 2014.
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Silk gland factor-2, involved in fibroin gene transcription, consists of LIM homeodomain, LIM-interacting, and single-stranded DNA-binding proteins.丝腺因子-2 参与丝氨酸基因转录,由 LIM 同源域、LIM 相互作用和单链 DNA 结合蛋白组成。
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In vitro transcription systems from cultured cells and fat-body tissue of the silkworm, Bombyx mori.来自家蚕(Bombyx mori)培养细胞和脂肪体组织的体外转录系统。
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Promoter sequence of fibroin gene assigned by in vitro transcription system.通过体外转录系统确定的丝心蛋白基因启动子序列。
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In vitro transcription from the adenovirus 2 major late promoter utilizing templates truncated at promoter-proximal sites.利用在启动子近端位点截短的模板,从腺病毒2型主要晚期启动子进行体外转录。
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7
Natural fibroin genes purified without using cloning procedures from fibroin-producing and -nonproducing tissues reveal indistinguishable structure and function.从产丝组织和非产丝组织中未经克隆程序纯化得到的天然丝素基因,其结构和功能并无差异。
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Upstream elements necessary for optimal function of the hsp 70 promoter in transformed flies.转化果蝇中hsp 70启动子最佳功能所需的上游元件。
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A tissue-specific transcription enhancer element is located in the major intron of a rearranged immunoglobulin heavy chain gene.一种组织特异性转录增强子元件位于重排的免疫球蛋白重链基因的主要内含子中。
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Nature. 1983;306(5943):557-61. doi: 10.1038/306557a0.