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RNA聚合酶II是一种糖蛋白。通过O-连接的N-乙酰葡糖胺对羧基末端结构域进行修饰。

RNA polymerase II is a glycoprotein. Modification of the COOH-terminal domain by O-GlcNAc.

作者信息

Kelly W G, Dahmus M E, Hart G W

机构信息

Department of Biological Chemistry, Johns Hopkins School of Medicine, Baltimore, Maryland 21205.

出版信息

J Biol Chem. 1993 May 15;268(14):10416-24.

PMID:8486697
Abstract

The largest subunit of mammalian RNA polymerase II (RNAP II) contains at its carboxyl terminus an unusual domain consisting of 52 tandem repeats of the consensus sequence Tyr-Ser-Pro-Thr-Ser-Pro-Ser. This domain, designated the COOH-terminal domain (CTD), is essential for viability and is extensively phosphorylated during the transition from preinitiation complex assembly to elongation (1). Indeed, phosphorylation of the CTD may play an important regulatory role in this transition. We show here that the CTD is also modified by a novel form of protein glycosylation, O-GlcNAc. This modification has been found on numerous transcription factors and other nuclear and cytosolic proteins (2). Glycopeptides obtained by proteolytic digestion of the CTD were purified by reverse-phase high performance liquid chromatography and sequenced. Results from such experiments suggest that glycosylation occurs at multiple sites throughout the CTD, similar to the phosphorylation of this domain. The carbohydrate, however, is not detectable on the phosphorylated form of the enzyme. This observation is consistent with the idea that phosphorylation and glycosylation are mutually exclusive modifications. The CTD of RNAP II, therefore, appears to exist in three distinct conformational states: unmodified, phosphorylated, and glycosylated. The differential modification of the CTD may play an important role in the regulated expression of genes transcribed by RNA polymerase II.

摘要

哺乳动物RNA聚合酶II(RNAP II)的最大亚基在其羧基末端含有一个由52个一致序列Tyr-Ser-Pro-Thr-Ser-Pro-Ser串联重复组成的特殊结构域。这个结构域被称为羧基末端结构域(CTD),对细胞生存力至关重要,并且在从起始前复合物组装到延伸的转变过程中会发生广泛的磷酸化(1)。实际上,CTD的磷酸化可能在这个转变过程中发挥重要的调节作用。我们在此表明,CTD也会被一种新型的蛋白质糖基化形式O-GlcNAc修饰。这种修饰已在众多转录因子以及其他核蛋白和胞质蛋白上被发现(2)。通过对CTD进行蛋白水解消化获得的糖肽经反相高效液相色谱纯化并测序。此类实验结果表明,糖基化发生在整个CTD的多个位点,类似于该结构域的磷酸化。然而,在该酶的磷酸化形式上检测不到碳水化合物。这一观察结果与磷酸化和糖基化是相互排斥的修饰这一观点一致。因此,RNAP II的CTD似乎以三种不同的构象状态存在:未修饰、磷酸化和糖基化。CTD的差异修饰可能在RNA聚合酶II转录的基因的调控表达中发挥重要作用。

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