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生物钟调控蛋白CCTR和衣藻蛋白1结合位点元件的体外诱变

In vitro mutagenesis of binding site elements for the clock-controlled proteins CCTR and Chlamy 1.

作者信息

Mittag M, Waltenberger H

机构信息

Botanisches Institut, Ludwig-Maximilians-Universität München, Germany.

出版信息

Biol Chem. 1997 Oct;378(10):1167-70.

PMID:9372186
Abstract

The luciferin-binding protein (LBP) from the dinoflagellate, Gonyaulax polyedra, is regulated by a circadian clock at the translational level. A 22-nucleotide long interval in the lbp 3' untranslated region, which contains seven UG-repeats, was characterized as a circadian cis-acting element, to which a clock controlled factor (CCTR) binds. Recently we have found that the phylogenetically distant green alga, Chlamydomonas reinhardtii, contains a CCTR analog, called Chlamy 1. Here we show that the flanking nucleotides surrounding the UG-repeats are required for high binding activity of CCTR and Chlamy 1. The absence of three or more UG-repeats abolishes binding with both proteins.

摘要

来自多甲藻(Gonyaulax polyedra)的荧光素结合蛋白(LBP)在翻译水平上受生物钟调控。lbp 3'非翻译区有一个22个核苷酸长的间隔区,其中包含七个UG重复序列,该区域被鉴定为昼夜节律顺式作用元件,生物钟控制因子(CCTR)可与之结合。最近我们发现,在系统发育上距离较远的绿藻莱茵衣藻(Chlamydomonas reinhardtii)中含有一种CCTR类似物,称为Chlamy 1。在此我们表明,UG重复序列周围的侧翼核苷酸是CCTR和Chlamy 1具有高结合活性所必需的。缺少三个或更多的UG重复序列会消除与这两种蛋白的结合。

相似文献

1
In vitro mutagenesis of binding site elements for the clock-controlled proteins CCTR and Chlamy 1.生物钟调控蛋白CCTR和衣藻蛋白1结合位点元件的体外诱变
Biol Chem. 1997 Oct;378(10):1167-70.
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引用本文的文献

1
The Involvement of hybrid cluster protein 4, HCP4, in Anaerobic Metabolism in Chlamydomonas reinhardtii.混合簇蛋白4(HCP4)参与莱茵衣藻的无氧代谢
PLoS One. 2016 Mar 1;11(3):e0149816. doi: 10.1371/journal.pone.0149816. eCollection 2016.
2
Ribonucleoprotein complexes that control circadian clocks.控制生物钟的核糖核蛋白复合体。
Int J Mol Sci. 2013 Apr 25;14(5):9018-36. doi: 10.3390/ijms14059018.
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The circadian RNA-binding protein CHLAMY 1 represents a novel type heteromer of RNA recognition motif and lysine homology domain-containing subunits.
昼夜节律RNA结合蛋白CHLAMY 1代表了一种新型的包含RNA识别基序和赖氨酸同源结构域亚基的异源二聚体。
Eukaryot Cell. 2004 Jun;3(3):815-25. doi: 10.1128/EC.3.3.815-825.2004.