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小鼠γ-晶状体蛋白基因的晶状体特异性启动子活性

Lens-specific promoter activity of a mouse gamma-crystallin gene.

作者信息

Lok S, Breitman M L, Chepelinsky A B, Piatigorsky J, Gold R J, Tsui L C

出版信息

Mol Cell Biol. 1985 Sep;5(9):2221-30. doi: 10.1128/mcb.5.9.2221-2230.1985.

Abstract

Crystallins are the major water-soluble proteins in vertebrate eye lenses. These lens-specific proteins are encoded by several gene families, and their expression is differentially regulated during lens cell differentiation. Here we show that a cloned mouse gamma-crystallin promoter is active in lens explants derived from 14-day-old chicken embryos but inactive in a variety of cells of non-lens origin. We also show that sequences required for proper utilization of this promoter are contained between nucleotide positions -392 and +47 relative to the transcription initiation site; deletion of sequences from positions -392 to -171 completely abolishes promoter activity. Since chickens do not have gamma-crystallin genes, the expression of a mouse gamma-crystallin promoter in chicken lens cells suggests that different classes of crystallin genes may be regulated by common lens tissue-specific mechanism(s) independent of species.

摘要

晶状体蛋白是脊椎动物眼晶状体中主要的水溶性蛋白质。这些晶状体特异性蛋白质由几个基因家族编码,并且它们的表达在晶状体细胞分化过程中受到差异调节。在这里我们表明,一个克隆的小鼠γ-晶状体蛋白启动子在源自14日龄鸡胚胎的晶状体外植体中具有活性,但在多种非晶状体来源的细胞中无活性。我们还表明,正确利用该启动子所需的序列包含在相对于转录起始位点的核苷酸位置-392至+47之间;从位置-392至-171删除序列会完全消除启动子活性。由于鸡没有γ-晶状体蛋白基因,小鼠γ-晶状体蛋白启动子在鸡晶状体细胞中的表达表明,不同类别的晶状体蛋白基因可能受独立于物种的共同晶状体组织特异性机制调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2c3/366947/3a29192a1c09/molcellb00105-0075-a.jpg

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