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编码色氨酰 - tRNA合成酶的人类基因:干扰素反应元件与外显子 - 内含子结构

The human gene encoding tryptophanyl-tRNA synthetase: interferon-response elements and exon-intron organization.

作者信息

Frolova L Y, Grigorieva A Y, Sudomoina M A, Kisselev L L

机构信息

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow.

出版信息

Gene. 1993 Jun 30;128(2):237-45. doi: 10.1016/0378-1119(93)90568-n.

Abstract

Recently, we cloned and sequenced the cDNA encoding human tryptophanyl-tRNA synthetase (hWRS) [Frolova et al., Gene 109 (1991) 291-296]. Independently, it has been shown that this protein is induced by interferons (IFN) gamma and alpha [Fleckner et al., Proc. Natl. Acad. Sci. USA 88 (1991) 11520-11524; Rubin et al., J. Biol. Chem. 266 (1991) 24245-24248]. This unusual feature of a housekeeping enzyme raises the problem of how the gene is regulated. Since at present the genomic structure of hWRS is unknown, this issue remains unsolved. Here, the exon-intron organization of hWRS has been deciphered. This gene consists of at least 12 exons that span more than 35 kb of DNA. At least two alternative noncoding exons precede ten coding exons. Upstream from the first exon, two GGAAAN(N/-)GAAA sequences, which are considered to be IFN-stimulating response elements (ISRE), have been revealed. The same consensus was also found in the intron region in close vicinity to the 5' end of the second exon. Thus, the IFN-stimulated synthesis of hWRS is presumably due to gene activation at the transcriptional level. Alignment of hWRS amino acid sequences has shown that exons V to XI of hWRS encode regions of structural similarity with bacterial WRS, whereas the N-terminal portion of the protein encoded by exons II to IV exhibits no homology with bacterial WRS.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

最近,我们克隆并测序了编码人色氨酰 - tRNA合成酶(hWRS)的cDNA[弗罗洛娃等人,《基因》109(1991) 291 - 296]。独立研究表明,这种蛋白质可被干扰素(IFN)γ和α诱导[弗莱克纳等人,《美国国家科学院院刊》88(1991) 11520 - 11524;鲁宾等人,《生物化学杂志》266(1991) 24245 - 24248]。这种管家酶的这一不寻常特性引发了该基因如何被调控的问题。由于目前hWRS的基因组结构未知,这个问题仍未解决。在此,hWRS的外显子 - 内含子组织已被破解。该基因由至少12个外显子组成,跨越超过35 kb的DNA。在十个编码外显子之前至少有两个可变的非编码外显子。在第一个外显子上游,已发现两个GGAAAN(N/-)GAAA序列,它们被认为是干扰素刺激反应元件(ISRE)。在第二个外显子5'端附近的内含子区域也发现了相同的共有序列。因此,hWRS受干扰素刺激的合成大概是由于转录水平上的基因激活。hWRS氨基酸序列的比对表明,hWRS的外显子V至XI编码与细菌WRS结构相似的区域,而外显子II至IV编码的蛋白质N端部分与细菌WRS无同源性。(摘要截短于250字)

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