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编码小鼠蛋白激酶CK2β亚基的基因结构

Structure of the gene encoding the murine protein kinase CK2 beta subunit.

作者信息

Boldyreff B, Issinger O G

机构信息

Universität des Saarlandes, Homburg/Saar, Germany.

出版信息

Genomics. 1995 Sep 1;29(1):253-6. doi: 10.1006/geno.1995.1239.

Abstract

The mouse protein kinase CK2 beta subunit gene (Csnk2b) is composed of seven exons contained within 7874 bp. The exon and intron lengths extend from 76 to 321 and 111 to 1272 bp, respectively. The lengths of the murine coding exons correspond exactly to the lengths of the exons in the human CK2 beta gene. Both genes contain a first untranslated exon. Also, the promoter regions from the human and murine CK2 beta gene share some common features, e.g., they contain neither a TATA nor a CAAT box, exon 1 is flanked by a cluster of CpG dinucleotides and recognition sequences for the HpaII restriction endonuclease, and several blocks of sequence in the 5' flanking region are conserved between mouse and human. Despite all of these common features, one of the most striking differences found concerns the human CK2 alpha subunit binding domain at position -170 to -239 of the human gene. This domain has no counterpart in the murine gene. Hence, regulation of transcription of the CK2 beta gene by the catalytic CK2 alpha subunit as was described by Robitzki et al. (J. Biol. Chem. 268: 5694-5703, 1993) for the human gene cannot be considered a general regulatory mechanism.

摘要

小鼠蛋白激酶CK2β亚基基因(Csnk2b)由7个外显子组成,位于7874 bp范围内。外显子和内含子长度分别从76至321 bp和111至1272 bp。小鼠编码外显子的长度与人CK2β基因中外显子的长度完全对应。两个基因均包含第一个非翻译外显子。此外,人和小鼠CK2β基因的启动子区域具有一些共同特征,例如,它们既不包含TATA框也不包含CAAT框,外显子1两侧是一串CpG二核苷酸和HpaII限制性内切酶的识别序列,并且5'侧翼区域中的几个序列块在小鼠和人之间是保守的。尽管有所有这些共同特征,但发现的最显著差异之一涉及人类基因中-170至-239位的人类CK2α亚基结合域。该结构域在小鼠基因中没有对应物。因此,如Robitzki等人(《生物化学杂志》268:5694 - 5703,1993)所描述的,催化性CK2α亚基对人类基因CK2β基因转录的调控不能被视为一种普遍的调控机制。

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