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通过图论方法鉴定脊柱裂的关键调控因子。

Identification of the Key Regulators of Spina Bifida Through Graph-Theoretical Approach.

作者信息

Tamkeen Naaila, AlOmar Suliman Yousef, Alqahtani Saeed Awad M, Al-Jurayyan Abdullah, Farooqui Anam, Tazyeen Safia, Ahmad Nadeem, Ishrat Romana

机构信息

Department of Biosciences, Jamia Millia Islamia, New Delhi, India.

Centre for Interdisciplinary Research in Basic Sciences, Jamia Millia Islamia, New Delhi, India.

出版信息

Front Genet. 2021 Apr 6;12:597983. doi: 10.3389/fgene.2021.597983. eCollection 2021.

Abstract

Spina Bifida (SB) is a congenital spinal cord malformation. Efforts to discern the key regulators (KRs) of the SB protein-protein interaction (PPI) network are requisite for developing its successful interventions. The architecture of the SB network, constructed from 117 manually curated genes was found to self-organize into a scale-free fractal state having a weak hierarchical organization. We identified three modules/motifs consisting of ten KRs, namely, , , , , , , , , , and . These KRs serve as the backbone of the network, they propagate signals through the different hierarchical levels of the network to conserve the network's stability while maintaining low popularity in the network. We also observed that the SB network exhibits a rich-club organization, the formation of which is attributed to our key regulators also except for and . The KRs that were found to ally with each other and emerge in the same motif, open up a new dimension of research of studying these KRs together. Owing to the multiple etiology and mechanisms of SB, a combination of several biomarkers is expected to have higher diagnostic accuracy for SB as compared to using a single biomarker. So, if all the KRs present in a single module/motif are targetted together, they can serve as biomarkers for the diagnosis of SB. Our study puts forward some novel SB-related genes that need further experimental validation to be considered as reliable future biomarkers and therapeutic targets.

摘要

脊柱裂(SB)是一种先天性脊髓畸形。识别SB蛋白质-蛋白质相互作用(PPI)网络的关键调节因子(KRs)对于开发成功的干预措施至关重要。由117个手动策划的基因构建的SB网络结构被发现自组织成一种具有弱层次组织的无标度分形状态。我们确定了由十个KRs组成的三个模块/基序,即 , , , , , , , , ,和 。这些KRs作为网络的主干,它们通过网络的不同层次传播信号,以保持网络的稳定性,同时在网络中保持低知名度。我们还观察到SB网络呈现出富俱乐部组织,其形成除了 和 之外也归因于我们的关键调节因子。被发现相互联合并出现在同一基序中的KRs,开启了一起研究这些KRs的新研究维度。由于SB的多种病因和机制,与使用单一生物标志物相比,几种生物标志物的组合预计对SB具有更高的诊断准确性。因此,如果针对单个模块/基序中存在的所有KRs,它们可以作为SB诊断的生物标志物。我们的研究提出了一些与SB相关的新基因,需要进一步的实验验证才能被视为可靠的未来生物标志物和治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/162c/8056047/5a12e48d5138/fgene-12-597983-g001.jpg

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