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参与家蚕丝基因表达的POU-M1/SGF-3基因的启动子。

Promoter of the POU-M1/SGF-3 gene involved in the expression of Bombyx silk genes.

作者信息

Xu P X, Fukuta M, Takiya S, Matsuno K, Xu X, Suzuki Y

机构信息

National Institute for Basic Biology, Okazaki, Japan.

出版信息

J Biol Chem. 1994 Jan 28;269(4):2733-42.

PMID:8300605
Abstract

To characterize the transcription regulation of the POU-M1/SGF-3 gene, we have cloned a genomic DNA fragment encompassing the whole coding region and its flanking sequences. This gene does not contain any intron. The 5'-flanking region of the gene contains several interesting motifs, such as homeodomain-binding motifs, sequences resembling the transcriptional factor Sp1-binding site, and TGTTT motifs, but lacks some of the typical transcriptional regulatory sequences, such as TATA and CCAAT boxes. Transcriptional analysis of a series of deletion mutants of the gene in the nuclear extracts prepared from the middle silk gland of 2-day-old fifth instar larvae revealed the presence of multiple cis-regulatory elements located both upstream and downstream of the initiation site. One of these elements, the homeodomain-binding element, was identified to mediate negative regulation. By mobility shift assay using the POU-M1 specific antibodies, we found that this negative element interacts with the POU-M1/SGF-3. Transcription analysis in vitro using templates mutagenized in the PB region and one of the POU-M1 antibodies indicated that the PB region is an autoregulatory element responsible for SGF-3-dependent transcriptional repression.

摘要

为了表征POU-M1/SGF-3基因的转录调控,我们克隆了一个包含整个编码区及其侧翼序列的基因组DNA片段。该基因不含任何内含子。该基因的5'侧翼区域包含几个有趣的基序,如同源结构域结合基序、类似于转录因子Sp1结合位点的序列和TGTTT基序,但缺少一些典型的转录调控序列,如TATA盒和CCAAT盒。对从2日龄五龄幼虫中部丝腺制备的核提取物中该基因的一系列缺失突变体进行转录分析,结果显示在起始位点的上游和下游均存在多个顺式调控元件。其中一个元件,即同源结构域结合元件,被确定介导负调控。通过使用POU-M1特异性抗体进行迁移率变动分析,我们发现这个负元件与POU-M1/SGF-3相互作用。使用在PB区域诱变的模板和一种POU-M1抗体进行的体外转录分析表明,PB区域是一个自调控元件,负责SGF-3依赖的转录抑制。

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