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一个拯救间接飞行肌和跳跃肌功能所必需的肌肉特异性内含子增强子调控果蝇原肌球蛋白I基因的表达。

A muscle-specific intron enhancer required for rescue of indirect flight muscle and jump muscle function regulates Drosophila tropomyosin I gene expression.

作者信息

Schultz J R, Tansey T, Gremke L, Storti R V

机构信息

Department of Biochemistry, University of Illinois College of Medicine, Chicago 60612.

出版信息

Mol Cell Biol. 1991 Apr;11(4):1901-11. doi: 10.1128/mcb.11.4.1901-1911.1991.

DOI:10.1128/mcb.11.4.1901-1911.1991
PMID:1706473
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC359871/
Abstract

The control of expression of the Drosophila melanogaster tropomyosin I (TmI) gene has been investigated by P-element transformation and rescue of the flightless and jumpless TmI mutant strain, Ifm(3)3. To localize cis-acting DNA sequences that control TmI gene expression, Ifm(3)3 flies were transformed with P-element plasmids containing various deletions and rearrangements of the TmI gene. The effects of these mutations on TmI gene expression were studied by analyzing both the extent of rescue of the Ifm(3)3 mutant phenotypes and determining TmI RNA levels in the transformed flies by primer extension analysis. The results of our analysis indicate that a region located within intron 1 of the gene is necessary and sufficient for directing muscle-specific TmI expression in the adult fly. This intron region has characteristics of a muscle regulatory enhancer element that can function in conjunction with the heterologous nonmuscle hsp70 promoter to promote rescue of the mutant phenotypes and to direct expression of an hsp70-Escherichia coli lacZ reporter gene in adult muscle. The enhancer can be subdivided further into two domains of activity based on primer extension analysis of TmI mRNA levels and on the rescue of mutant phenotypes. One of the intron domains is required for expression in the indirect flight muscle of the adult. The function of the second domain is unknown, but it could regulate the level of expression or be required for expression in other muscle.

摘要

通过P因子转化以及对飞行缺失和跳跃缺失的肌动蛋白原肌球蛋白I(TmI)突变株Ifm(3)3进行拯救,研究了黑腹果蝇肌动蛋白原肌球蛋白I(TmI)基因的表达调控。为了定位控制TmI基因表达的顺式作用DNA序列,用含有TmI基因各种缺失和重排的P因子质粒转化Ifm(3)3果蝇。通过分析Ifm(3)3突变表型的拯救程度以及通过引物延伸分析确定转化果蝇中TmI RNA水平,研究了这些突变对TmI基因表达的影响。我们的分析结果表明,位于该基因内含子1内的一个区域对于指导成年果蝇中肌肉特异性TmI表达是必需且充分的。这个内含子区域具有肌肉调节增强子元件的特征,它可以与异源非肌肉hsp70启动子协同作用,以促进突变表型的拯救,并指导hsp70-大肠杆菌lacZ报告基因在成年肌肉中的表达。基于对TmI mRNA水平的引物延伸分析以及突变表型的拯救,该增强子可进一步细分为两个活性结构域。其中一个内含子结构域是成年果蝇间接飞行肌中表达所必需的。第二个结构域的功能尚不清楚,但它可能调节表达水平或在其他肌肉的表达中是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/359871/5a741f76800f/molcellb00138-0144-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/359871/22cfe98f2e21/molcellb00138-0141-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/359871/5a741f76800f/molcellb00138-0144-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/359871/22cfe98f2e21/molcellb00138-0141-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ce8/359871/5a741f76800f/molcellb00138-0144-a.jpg

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