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哺乳动物晶状体中的微小RNA(miRNA)与Dicer:脑特异性miRNA在晶状体中的表达

miRNA and Dicer in the mammalian lens: expression of brain-specific miRNAs in the lens.

作者信息

Frederikse Peter H, Donnelly Robert, Partyka Lukasz M

机构信息

Department of Pharmacology and Physiology, UMDNJ New Jersey Medical School , 185 South Orange Ave MSB H-64 , Newark, NJ 07103, USA.

出版信息

Histochem Cell Biol. 2006 Jul;126(1):1-8. doi: 10.1007/s00418-005-0139-0. Epub 2006 Jan 6.

Abstract

Micro RNAs (miRNAs) are approximately 22 nucleotide molecules that regulate gene expression post-transcriptionally and govern a wide range of physiological and developmental processes. Evidence now indicates that miRNAs can also coordinately down-regulate transcript levels for very large groups of genes in a tissue-specific manner, in addition to their ability to suppress protein translation. Here, we examine expression of specific miRNAs and Dicer ribonuclease that is required for miRNA biogenesis in mouse and rat lenses. Northern blot analysis demonstrated lens expression of brain-specific miR-124 and miR-7 in lenses, as well as miR-125b and let-7a. In addition, we provide evidence that muscle specific miR-1 is not present in lens. We detected Dicer transcripts in 21 day, 6 week, and 1 year mouse lenses and 15 day rat lens, and detected Dicer protein in adult lens protein samples. Immunohistochemical examination of late embryonic, post-natal, and adult rat lens sections identified expression of Dicer in differentiating fiber cells that undergo pronounced cell elongation in the lens interior and anterior epithelial cells. The present study provides evidence that miRNAs, which include brain-specific forms, and Dicer are expressed in mammalian lenses, indicating that fundamental aspects of miRNA biology are utilized by the lens during late embryonic and post-natal development and in adult lenses.

摘要

微小RNA(miRNA)是约22个核苷酸的分子,可在转录后调节基因表达,并控制广泛的生理和发育过程。现在有证据表明,miRNA除了能够抑制蛋白质翻译外,还能以组织特异性方式协同下调非常大的基因群体的转录水平。在这里,我们研究了小鼠和大鼠晶状体中miRNA生物合成所需的特定miRNA和Dicer核糖核酸酶的表达。Northern印迹分析表明,晶状体中表达脑特异性miR-124和miR-7,以及miR-125b和let-7a。此外,我们提供证据表明晶状体中不存在肌肉特异性miR-1。我们在21日龄、6周龄和1岁的小鼠晶状体以及15日龄的大鼠晶状体中检测到Dicer转录本,并在成年晶状体蛋白样品中检测到Dicer蛋白。对晚期胚胎、出生后和成年大鼠晶状体切片的免疫组织化学检查确定,Dicer在晶状体内部经历明显细胞伸长的分化纤维细胞和前上皮细胞中表达。本研究提供证据表明,包括脑特异性形式的miRNA和Dicer在哺乳动物晶状体中表达,这表明miRNA生物学的基本方面在胚胎晚期和出生后发育以及成年晶状体中被晶状体所利用。

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