Panina Ekaterina M, Mironov Andrey A, Gelfand Mikhail S
State Scientific Center GosNIIGenetika, 1st Dorozhny Proezd 1, Moscow 113545, Russia.
Proc Natl Acad Sci U S A. 2003 Aug 19;100(17):9912-7. doi: 10.1073/pnas.1733691100. Epub 2003 Aug 6.
Zinc is an important component of many proteins, but in large concentrations it is poisonous to the cell. Thus its transport is regulated by zinc repressors ZUR of proteobacteria and Gram-positive bacteria from the Bacillus group and AdcR of bacteria from the Streptococcus group. Comparative computational analysis allowed us to identify binding signals of ZUR repressors GAAATGTTATANTATAACATTTC for gamma-proteobacteria, GTAATGTAATAACATTAC for the Agrobacterium group, GATATGTTATAACATATC for the Rhododoccus group, TAAATCGTAATNATTACGATTTA for Gram-positive bacteria, and TTAACYRGTTAA of the streptococcal AdcR repressor. In addition to known transporters and their paralogs, zinc regulons were predicted to contain a candidate component of the ATP binding cassette, zinT (b1995 in Escherichia coli and yrpE in Bacillus subtilis). Candidate AdcR-binding sites were identified upstream of genes encoding pneumococcal histidine triad (PHT) proteins from a number of pathogenic streptococci. Protein functional analysis of this family suggests that PHT proteins are involved in the invasion process. Finally, repression by zinc was predicted for genes encoding a variety of paralogs of ribosomal proteins. The original copies of all these proteins contain zinc-ribbon motifs and thus likely bind zinc, whereas these motifs are destroyed in zinc-regulated paralogs. We suggest that the induction of these paralogs in conditions of zinc starvation leads to their incorporation in a fraction of ribosomes instead of the original ribosomal proteins; the latter are then degraded with subsequent release of some zinc for the utilization by other proteins. Thus we predict a mechanism for maintaining zinc availability for essential enzymes.
锌是许多蛋白质的重要组成部分,但高浓度的锌对细胞有毒。因此,其运输受到来自变形杆菌和芽孢杆菌属革兰氏阳性菌的锌阻遏物ZUR以及链球菌属细菌的AdcR的调控。比较计算分析使我们能够确定γ-变形杆菌的ZUR阻遏物GAAATGTTATANTATAACATTTC、农杆菌属的GTAATGTAATAACATTAC、红球菌属的GATATGTTATAACATATC、革兰氏阳性菌的TAAATCGTAATNATTACGATTTA以及链球菌AdcR阻遏物的TTAACYRGTTAA的结合信号。除了已知的转运蛋白及其旁系同源物外,锌调控子预计还包含一个ATP结合盒的候选成分zinT(大肠杆菌中的b1995和枯草芽孢杆菌中的yrpE)。在许多致病性链球菌编码肺炎球菌组氨酸三联体(PHT)蛋白的基因上游鉴定出了候选的AdcR结合位点。对该家族的蛋白质功能分析表明,PHT蛋白参与了入侵过程。最后,预计锌会对编码各种核糖体蛋白旁系同源物的基因产生抑制作用。所有这些蛋白质的原始拷贝都含有锌带基序,因此可能结合锌,而这些基序在锌调控的旁系同源物中被破坏。我们认为,在锌饥饿条件下这些旁系同源物的诱导会导致它们掺入一部分核糖体中,而不是原始的核糖体蛋白;然后后者会被降解,随后释放出一些锌供其他蛋白质利用。因此,我们预测了一种维持必需酶锌可用性的机制。