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人类和小鼠脱氧胞苷激酶基因中的保守基因结构和转录因子位点。

Conserved gene structure and transcription factor sites in the human and mouse deoxycytidine kinase genes.

作者信息

Johansson M, Norda A, Karlsson A

机构信息

Division of Clinical Virology, Karolinska Institute, Huddinge University Hospital, S-141 86, Stockholm, Sweden.

出版信息

FEBS Lett. 2000 Dec 29;487(2):209-12. doi: 10.1016/s0014-5793(00)02347-4.

Abstract

Deoxycytidine kinase (dCK) phosphorylates several anti-cancer and anti-viral nucleoside analogs. The enzyme is predominantly expressed in lymphoid tissues regulated by an unknown mechanism. We have cloned and sequenced the 20 kbp mouse dCK gene and approximately 1.7 kbp of the 5' flanking regions of both the human and mouse dCK genes. Five major inter-species conserved motifs were identified in the 5' region including the transcription initiation region, an SP1 site and two closely located putative octamer transcription factor sites. Luciferase reporter experiments showed that the human dCK 5' region efficiently initiated transcription but no tissue regulatory element could be identified.

摘要

脱氧胞苷激酶(dCK)可磷酸化多种抗癌和抗病毒核苷类似物。该酶主要在淋巴组织中表达,其调控机制尚不清楚。我们已经克隆并测序了20千碱基对的小鼠dCK基因以及人和小鼠dCK基因5'侧翼区域约1.7千碱基对的序列。在5'区域鉴定出五个主要的种间保守基序,包括转录起始区域、一个SP1位点和两个紧密相邻的假定八聚体转录因子位点。荧光素酶报告实验表明,人dCK 5'区域能有效启动转录,但未发现组织调控元件。

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