摘要
目的: 蛋白质去甲酰化是转录后最重要和最普遍的修饰之一。越来越多的证据表明,SENP(Sentrin/Sumospecific蛋白酶)对目标蛋白的SUMO修饰的稳态水平至关重要,蛋白质去SUMO化调节包括转录、发育、分化、神经保护以及发病机制在内的多种生物过程。在脊椎动物的眼睛中,我们和其他人之前已经表明,SUMOYLATION参与了包括视网膜和晶状体在内的主要眼部组织的分化。然而,七种SENP酶:SENP1-3和SENP5-8在眼部组织中的生物学意义尚未得到充分研究。 方法: 在含有胎牛血清(FBS)或兔血清(RBS)和1%青霉素-链霉素的Dulbecco改良Eagle''s培养基(DMEM)中培养5个主要眼细胞系。用qRT-PCR分析mRNA水平。蛋白质水平用蛋白质印迹分析法测定,并用图像J定量。 结果: 在mRNA水平上,所有的SENP在视网膜高度表达,角膜、晶状体上皮和晶状体纤维的表达模式大大降低。在蛋白水平上,SENP1-3、SENP6在角膜中含量丰富,SENP5、SENP7、SENP8在视网膜中含量丰富,在晶状体组织中含量相对较少。 结论: 我们的结果首次建立了7种去甲酰化酶(SENP)的分化表达模式,为进一步研究脊椎动物眼的蛋白质去甲酰化功能提供了依据。
关键词: SUMO化修饰,去SUMO化修饰,SENP,视网膜,镜头,角膜
Current Molecular Medicine
Title:Differential Expression of Seven De-sumoylation Enzymes (SENPs) in Major Ocular Tissues of Mouse Eye
Volume: 18 Issue: 8
关键词: SUMO化修饰,去SUMO化修饰,SENP,视网膜,镜头,角膜
摘要: Purpose: Protein Sumoylation is one of the most important and prevalent posttranscriptional modification. Increasing evidence have shown that the SENPs (sentrin/SUMOspecific proteases) are critical for steady-state levels of SUMO modification of target proteins, and protein de-sumoylation modulates a great diversity of biological processes including transcription, development, differentiation, neuroprotection, as well as pathogenesis. In the vertebrate eye, we and others have previously shown that sumoylation participated in the differentiation of major ocular tissues including retina and lens. However, the biological significance of seven SENP enzymes: SENP1 to 3 and SENP5 to 8 have not be fully investigated in the ocular tissues.
Methods: The 5 major ocular cell lines were cultured in Dulbecco’s modified Eagle’s medium (DMEM) containing fetal bovine serum (FBS) or rabbit serum (RBS) and 1% Penicillin- Streptomycin. The mRNA levels were analysed with qRT-PCR. The protein levels were determined with western blot analysis and quantitated with Image J.
Results: At the mRNA level, all SENPs were highly expressed in retina, and much reduced expression patterns in cornea, lens epithelium and lens fiber. At the protein level, SENP1 to -3, and SENP6 were highly abundant in cornea, while SENP5, SENP7 and SENP8 were enriched in retina, and these SENPs were relatively less abundant in lens tissues.
Conclusion: Our results for the first time established the differentiation expression patterns of the 7 de-sumoylation enzymes (SENPs), which provides a basis for further investigation of protein desumoylation functions in vertebrate eye.
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Cite this article as:
Differential Expression of Seven De-sumoylation Enzymes (SENPs) in Major Ocular Tissues of Mouse Eye, Current Molecular Medicine 2018; 18 (8) . https://dx.doi.org/10.2174/1566524019666190112132103
DOI https://dx.doi.org/10.2174/1566524019666190112132103 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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