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不断演变的Notch多聚谷氨酰胺序列揭示了可能的螺线管干扰元件。

Evolving Notch polyQ tracts reveal possible solenoid interference elements.

作者信息

Erives Albert J

机构信息

Department of Biology University of Iowa Iowa City, IA, United States of America.

出版信息

PLoS One. 2017 Mar 20;12(3):e0174253. doi: 10.1371/journal.pone.0174253. eCollection 2017.

Abstract

Polyglutamine (polyQ) tracts in regulatory proteins are extremely polymorphic. As functional elements under selection for length, triplet repeats are prone to DNA replication slippage and indel mutations. Many polyQ tracts are also embedded within intrinsically disordered domains, which are less constrained, fast evolving, and difficult to characterize. To identify structural principles underlying polyQ tracts in disordered regulatory domains, here I analyze deep evolution of metazoan Notch polyQ tracts, which can generate alleles causing developmental and neurogenic defects. I show that Notch features polyQ tract turnover that is restricted to a discrete number of conserved "polyQ insertion slots". Notch polyQ insertion slots are: (i) identifiable by an amphipathic "slot leader" motif; (ii) conserved as an intact C-terminal array in a 1-to-1 relationship with the N-terminal solenoid-forming ankyrin repeats (ARs); and (iii) enriched in carboxamide residues (Q/N), whose sidechains feature dual hydrogen bond donor and acceptor atoms. Correspondingly, the terminal loop and β-strand of each AR feature conserved carboxamide residues, which would be susceptible to folding interference by hydrogen bonding with residues outside the ARs. I thus suggest that Notch polyQ insertion slots constitute an array of AR interference elements (ARIEs). Notch ARIEs would dynamically compete with the delicate serial folding induced by adjacent ARs. Huntingtin, which harbors solenoid-forming HEAT repeats, also possesses a similar number of polyQ insertion slots. These results suggest that intrinsically disordered interference arrays featuring carboxamide and polyQ enrichment may constitute coupled proteodynamic modulators of solenoids.

摘要

调控蛋白中的聚谷氨酰胺(polyQ)序列具有极高的多态性。作为受长度选择的功能元件,三联体重复序列容易发生DNA复制滑移和插入缺失突变。许多polyQ序列还嵌入在内在无序结构域中,这些结构域约束较少、进化迅速且难以表征。为了确定无序调控结构域中polyQ序列背后的结构原理,在此我分析了后生动物Notch polyQ序列的深度进化,其可产生导致发育和神经源性缺陷的等位基因。我发现Notch具有polyQ序列周转现象,该现象仅限于数量有限的保守“polyQ插入位点”。Notch polyQ插入位点具有以下特点:(i)可通过两亲性“位点引导”基序识别;(ii)作为完整的C端阵列保守存在,与形成N端螺线管的锚蛋白重复序列(ARs)呈1对1关系;(iii)富含羧酰胺残基(Q/N),其侧链具有双氢键供体和受体原子。相应地,每个AR的末端环和β链具有保守的羧酰胺残基,这些残基可能会因与ARs外部残基形成氢键而受到折叠干扰。因此,我认为Notch polyQ插入位点构成了一系列AR干扰元件(ARIEs)。Notch ARIEs将与相邻ARs诱导的精细序列折叠动态竞争。含有形成螺线管状HEAT重复序列的亨廷顿蛋白也具有类似数量的polyQ插入位点。这些结果表明,富含羧酰胺和polyQ的内在无序干扰阵列可能构成螺线管的耦合蛋白质动力学调节剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee2e/5358852/0a174d1941c9/pone.0174253.g001.jpg

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