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果蝇原肌球蛋白表达的微小差异对肌肉功能有显著影响。

Small differences in Drosophila tropomyosin expression have significant effects on muscle function.

作者信息

Tansey T, Schultz J R, Miller R C, 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 Dec;11(12):6337-42. doi: 10.1128/mcb.11.12.6337-6342.1991.

DOI:10.1128/mcb.11.12.6337-6342.1991
PMID:1719381
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC361830/
Abstract

The effects of promoter deletions on Drosophila tropomyosin I (TmI) gene expression have been determined by measuring TmI RNA levels in transformed flies. Decreases in RNA levels have been correlated with rescue of flightless and jumpless mutant phenotypes in Ifm(3)3 mutant transformed flies and changes in muscle ultrastructure. The results of this analysis have allowed us to identify a region responsible for 20% of maximal TmI expression, estimate threshold levels of TmI RNA required for indirect flight and jump muscle function, and obtain evidence suggesting that sarcomere length may be an important determinant of flight muscle function.

摘要

通过测量转基因果蝇中肌动蛋白抑制蛋白I(TmI)的RNA水平,已确定启动子缺失对果蝇肌动蛋白抑制蛋白I(TmI)基因表达的影响。RNA水平的降低与Ifm(3)3突变转基因果蝇中无飞行能力和无跳跃能力突变表型的挽救以及肌肉超微结构的变化相关。该分析结果使我们能够确定一个负责最大TmI表达20%的区域,估计间接飞行和跳跃肌肉功能所需的TmI RNA阈值水平,并获得证据表明肌节长度可能是飞行肌肉功能的重要决定因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f56c/361830/d1a561f5fbbc/molcellb00036-0552-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f56c/361830/172b093dcafb/molcellb00036-0551-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f56c/361830/d1a561f5fbbc/molcellb00036-0552-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f56c/361830/172b093dcafb/molcellb00036-0551-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f56c/361830/d1a561f5fbbc/molcellb00036-0552-a.jpg

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本文引用的文献

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A transposable P vector that confers selectable G418 resistance to Drosophila larvae.一个可转座的 P 载体,赋予果蝇幼虫可选择的 G418 抗性。
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A non-flight muscle isoform of Drosophila tropomyosin rescues an indirect flight muscle tropomyosin mutant.果蝇原肌球蛋白的一种非飞行肌同种型拯救了间接飞行肌原肌球蛋白突变体。
J Muscle Res Cell Motil. 1993 Feb;14(1):85-98. doi: 10.1007/BF00132183.
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Transformation of Drosophila melanogaster with the wild-type myosin heavy-chain gene: rescue of mutant phenotypes and analysis of defects caused by overexpression.用野生型肌球蛋白重链基因转化黑腹果蝇:突变表型的拯救及过表达引起的缺陷分析。
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影响间接飞行肌肌原纤维蛋白的果蝇飞行缺失突变体的分离。
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Two Drosophila actin genes in detail. Gene structure, protein structure and transcription during development.详细介绍两个果蝇肌动蛋白基因。基因结构、蛋白质结构及发育过程中的转录。
J Mol Biol. 1983 Feb 5;163(4):533-51. doi: 10.1016/0022-2836(83)90111-0.
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Transposition of cloned P elements into Drosophila germ line chromosomes.克隆的P因子向果蝇种系染色体的转座。
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The white gene as a marker in a new P-element vector for gene transfer in Drosophila.白色基因作为一种标记,用于果蝇基因转移的新型P因子载体中。
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EMBO J. 1987 May;6(5):1375-85. doi: 10.1002/j.1460-2075.1987.tb02378.x.
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Context-dependent gene expression: cis-acting negative effects of specific procaryotic plasmid sequences on eucaryotic genes.上下文依赖的基因表达:特定原核质粒序列对真核基因的顺式作用负效应
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An insertion within a variably spliced Drosophila tropomyosin gene blocks accumulation of only one encoded isoform.果蝇原肌球蛋白基因可变剪接区域内的一个插入片段仅阻止一种编码异构体的积累。
Cell. 1985 May;41(1):57-66. doi: 10.1016/0092-8674(85)90061-3.