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果蝇黏液蛋白基因Sgs-3的阶段和组织特异性启动子元件的精细结构突变分析。

Fine-structure mutational analysis of a stage- and tissue-specific promoter element of the Drosophila glue gene Sgs-3.

作者信息

Todo T, Roark M, Raghavan K V, Mayeda C, Meyerowitz E

机构信息

Division of Biology, California Institute of Technology, Pasadena 91125.

出版信息

Mol Cell Biol. 1990 Nov;10(11):5991-6002. doi: 10.1128/mcb.10.11.5991-6002.1990.

Abstract

The Sgs-3 gene of Drosophila melanogaster exhibits a tightly regulated pattern of expression governed by two functionally equivalent elements within 1 kb of the gene, each of which is sufficient to confer third-instar salivary gland-specific transcription. In this report we describe a detailed functional analysis of one of these, the proximal element. To determine the nucleotides responsible for specific expression, we have introduced mutations into the proximal element and then assessed the effects of each alteration on expression in the developing animal. We have identified six particularly important base pairs which are located in two regions separated by nonessential sequences. These base pairs, along with some surrounding sequence, are conserved within the upstream regions of the three glue genes at 68C. Nearly identical groups of base pairs can be found upstream of the other glue genes which have been cloned. This analysis has allowed us to derive a consensus sequence, which we believe contains binding sites for two different factors which interact to direct third-instar salivary gland-specific expression.

摘要

黑腹果蝇的Sgs-3基因呈现出一种受严格调控的表达模式,该模式由基因1 kb范围内的两个功能等效元件控制,每个元件都足以赋予三龄幼虫唾液腺特异性转录。在本报告中,我们描述了其中一个元件——近端元件的详细功能分析。为了确定负责特异性表达的核苷酸,我们在近端元件中引入了突变,然后评估了每种改变对发育中动物表达的影响。我们确定了六个特别重要的碱基对,它们位于由非必需序列隔开的两个区域。这些碱基对以及一些周围序列在68C处的三个胶蛋白基因的上游区域中是保守的。在已克隆的其他胶蛋白基因的上游可以发现几乎相同的碱基对组。该分析使我们能够得出一个共有序列,我们认为该序列包含两个不同因子的结合位点,这两个因子相互作用以指导三龄幼虫唾液腺特异性表达。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4712/361397/97f258c2223f/molcellb00047-0406-a.jpg

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