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N-乙酰葡糖胺基转移酶V mRNA在哺乳动物组织和细胞系中的表达。

Expression of N-acetylglucosaminyltransferase V mRNA in mammalian tissues and cell lines.

作者信息

Perng G S, Shoreibah M, Margitich I, Pierce M, Fregien N

机构信息

Department of Cell Biology & Anatomy, University of Miami School of Medicine, FL, USA.

出版信息

Glycobiology. 1994 Dec;4(6):867-71. doi: 10.1093/glycob/4.6.867.

Abstract

The expression of N-acetylglucosaminyltransferase V (Glc-NAc-T V) is increased in many oncogenically transformed cells and in cell lines which are induced to proliferate. In order to characterize the regulation of GlcNAc-T V at the molecular level, we have examined the expression of Glc-NAc-T V mRNAs in a number of mouse tissues and in several human and rodent cell lines. The GlcNAc-T V mRNA is expressed in different amounts in the various mouse tissues, with the greatest amount observed in brain, followed by thymus, kidney, lung, intestine, heart and stomach, and no transcripts detected in liver or skeletal muscle. Measurements of GlcNAc-T V enzymatic activity, by contrast, show brain to have lower levels of activity than several of the other tissues, suggesting possible post-translational regulation. We find that there are two GlcNAc-T V transcripts in most of the RNAs analysed. The rodent cell lines all express both a 7.5 and a 9.5 kb mRNA, with the smaller transcript being more abundant. The human cells have mRNAs of 4.5 and 9.5 kb. Both mRNAs are expressed in HepG2 and MCF-7 cells, while A431 cells express only the 4.5 kb mRNA and HL60 cells express only the 9.5 kb transcript. Furthermore, only the 9.5 kb mRNA appears to be increased, along with activity, when HepG2 cells are stimulated to proliferate, suggesting that the two mRNAs may be under different regulatory controls. Also, a GlcNAc-T V-deficient, mutant lymphoma cell line, PHAR2.1, was found to express mRNAs which are larger than the normal mRNAs, possible due to an insertion or aberrant splicing, resulting in a defective mRNA.

摘要

N-乙酰葡糖胺基转移酶V(Glc-NAc-T V)在许多致癌转化细胞和诱导增殖的细胞系中表达增加。为了在分子水平上表征GlcNAc-T V的调控,我们检测了Glc-NAc-T V mRNA在多种小鼠组织以及几种人类和啮齿动物细胞系中的表达。GlcNAc-T V mRNA在不同的小鼠组织中表达量不同,在脑中观察到的量最大,其次是胸腺、肾脏、肺、肠、心脏和胃,在肝脏或骨骼肌中未检测到转录本。相比之下,GlcNAc-T V酶活性的测量表明,脑的活性水平低于其他几种组织,这表明可能存在翻译后调控。我们发现在大多数分析的RNA中有两种GlcNAc-T V转录本。啮齿动物细胞系均表达7.5 kb和9.5 kb的mRNA,较小的转录本更为丰富。人类细胞有4.5 kb和9.5 kb的mRNA。两种mRNA在HepG2和MCF-7细胞中均有表达,而A431细胞仅表达4.5 kb的mRNA,HL60细胞仅表达9.5 kb的转录本。此外,当HepG2细胞被刺激增殖时,只有9.5 kb的mRNA似乎与活性一起增加,这表明这两种mRNA可能受到不同的调控。此外,发现一种GlcNAc-T V缺陷的突变淋巴瘤细胞系PHAR2.1表达的mRNA比正常mRNA大,可能是由于插入或异常剪接导致mRNA有缺陷。

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