Motifs enable communication efficiency and fault-tolerance in transcriptional networks

被引:4
|
作者
Roy, Satyaki [4 ]
Ghosh, Preetam [2 ]
Barua, Dipak [3 ]
Das, Sajal K. [1 ]
机构
[1] Missouri Univ Sci & Technol, Dept Comp Sci, Rolla, MO 65409 USA
[2] Virginia Commonwealth Univ, Dept Comp Sci, Richmond, VA 23284 USA
[3] Missouri Univ Sci & Technol, Dept Chem Engn, Rolla, MO 65409 USA
[4] Univ N Carolina, Chapel Hill, NC 27515 USA
基金
美国国家科学基金会;
关键词
EARLY-LIFE STRESS; REGULATORY NETWORKS; GENE KNOCKOUT; INSTABILITY; EXPRESSION; PHENOTYPES; PATHWAYS; DRIVEN; CANCER; BRCA1;
D O I
10.1038/s41598-020-66573-x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Analysis of the topology of transcriptional regulatory networks (TRNs) is an effective way to study the regulatory interactions between the transcription factors (TFs) and the target genes. TRNs are characterized by the abundance of motifs such as feed forward loops (FFLs), which contribute to their structural and functional properties. In this paper, we focus on the role of motifs (specifically, FFLs) in signal propagation in TRNs and the organization of the TRN topology with FFLs as building blocks. To this end, we classify nodes participating in FFLs (termed motif central nodes) into three distinct roles (namely, roles A, B and C), and contrast them with TRN nodes having high connectivity on the basis of their potential for information dissemination, using metrics such as network efficiency, path enumeration, epidemic models and standard graph centrality measures. We also present the notion of a three tier architecture and how it can help study the structural properties of TRN based on connectivity and clustering tendency of motif central nodes. Finally, we motivate the potential implication of the structural properties of motif centrality in design of efficient protocols of information routing in communication networks as well as their functional properties in global regulation and stress response to study specific disease conditions and identification of drug targets.
引用
收藏
页数:15
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