摘要
目的:蛋白质去甲酰化是控制染色质结构动力学、基因表达转录调控、细胞增殖与分化、细胞转化与癌变、自噬与衰老等多种细胞过程的成熟调控机制。在脊椎动物的视觉系统中,我们和其他人已经发现,在眼睛发育过程中,SUMOYLATION在调节几种眼部组织的分化中起着重要作用。为了进一步阐明磺化作用的作用机理,需要体外检测系统。目前,αTN4-1, FHL124, HLE, N/N1003A 和 ARPE-19等5种主要细胞系已被广泛应用于正常视觉生理和各种疾病过程的生化和分子方面的检测。因此,我们对这三种类型的苏门答腊酶、激活酶SAE1和UBA2、结合酶UBC9和结扎酶(如RanBP2 和 PIAS1)在这些眼细胞系中的表达模式进行了研究。 方法:用含胎牛血清(FBS)、兔血清(RBS)和1%青霉素-链霉素的杜尔贝科改良伊格尔培养基(DMEM)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:我们得到如下结果:1)对于编码E1 SAE1 和 UBA2, E2 UBC9 和 E3 PIAS1的mRNAs,在αtn4-1细胞中的表达水平最高;对于编码RanBP2的mRNa,在n/n1003a细胞中的表达水平最高;2)与mRNa的表达模式相比,SAE1的表达水平相似。在所有5个细胞系中都观察到了蛋白质,除N/N1003A外,所有细胞中的UBA2蛋白都是如此,其中与其他细胞系相比,UBA2蛋白的富集量超过了4倍;3)除N/N1003A细胞外,所有细胞均检测到类似水平的UBC9蛋白,其中UBC9水平较其他细胞系下降了一倍以上;4)对于E3连接酶,我们没有发现N/N1003A细胞中有规则的PIAS1带,其余细胞中的PIAS1水平相差小于0.6倍;所有细胞中的PIAS1水平均高于其他细胞系。除FHL124细胞外,其他细胞的RanBP2水平相似,在FHL124细胞中,RanBP2下降了70%。 结论:我们对5种眼细胞株中三种类型的去甲酰化酶的差异表达模式的测定有助于了解脊椎动物眼的去甲酰化功能。
关键词: SAE1
Current Molecular Medicine
Title:Analysis of the Differential Expression Patterns of Sumoylation Enzymes E1, E2 and E3 in Ocular Cell Lines
Volume: 18 Issue: 8
关键词: SAE1
摘要: Purpose: Protein sumoylation is a well established regulatory mechanism to control many cellular processes such as chromatin structure dynamics, transcriptional regulation of gene expression, cell proliferation and differentiation, cell transformation and carcinogenesis, autophagy and senescence. In the vertebrate vision system, we and others have revealed that sumoylation plays important roles in regulating differentiation of several ocular tissues during eye development. To further elucidate the functional mechanisms of sumoylation, in vitro assay systems are needed. Currently, the five major cell lines including αTN4-1, FHL124, HLE, N/N1003A and ARPE-19 have been extensively used to test the biochemical and molecular aspects of normal vision physiology and various disease processes. Thus, we conducted the study on the expression patterns of the three types of sumoylation enzymes, the activating enzymes SAE1 and UBA2, the conjugating enzyme UBC9, and the ligating enzymes such as RanBP2 and PIAS1 in these ocular cell lines.
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: we have obtained the following results: 1) For the mRNAs encoding E1 SAE1 and UBA2, E2 UBC9 and E3 PIAS1, the highest level of expression was observed in αTN4-1 cells; For the mRNA encoding RanBP2, the highest level of expression was detected in N/N1003A cells; 2) In contrast to the mRNA expression patterns, a similar level of the SAE1 protein was observed in the all five cell lines, and so is true with UBA2 protein in all cells except for N/N1003A where over fourfold of enrichment in UBA2 protein was observed compared with other cell lines; 3) A similar level of UBC9 protein was also detected in all cells except for N/N1003A where more than one-fold of decrease in UBC9 level was found compared with other cell lines; 4) For E3 ligases, we did not identify the regular PIAS1 band in N/N1003A cells, the remaining cells have a level of PIAS1 with difference of less than 0.6-fold; all cells except for FHL124 cells have a similar level of RanBP2, and a 70% drop in RanBP2 was observed in FHL124 cell.
Conclusions: Our determination of the differential expression patterns of the three types of sumoylation enzymes in the 5 ocular cell lines help to understand sumoylation functions in vertebrate eye.
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Cite this article as:
Analysis of the Differential Expression Patterns of Sumoylation Enzymes E1, E2 and E3 in Ocular Cell Lines, Current Molecular Medicine 2018; 18 (8) . https://dx.doi.org/10.2174/1566524019666190112143636
DOI https://dx.doi.org/10.2174/1566524019666190112143636 |
Print ISSN 1566-5240 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-5666 |
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