一个mi-RNA通路间调控基序的系统分析。

Stefano Di Carlo, Gianfranco Politano, Alessandro Savino, Alfredo Benso
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引用次数: 13

摘要

背景:小非编码rna的新类型和新功能的不断发现表明,调控机制的存在远比目前用于研究和设计基因调控网络的机制复杂得多。仅关注微rna (miRNAs)的作用,它们已被发现是几个通路内调控基序的一部分。然而,通路间调控机制往往被忽视,需要进一步研究。结果:在本文中,我们提出了一项系统生物学研究的结果,旨在分析一种称为通路保护环的高级通路间调控基序,该基序以前没有描述过,其中mirna似乎在通路的成功行为和激活中起着至关重要的作用。通过对大量公共数据库的自动分析,我们发现统计证据表明,这种通路间调控基序在几种KEGG智人通路中非常常见,并且共同创建了一个复杂的调控网络,涉及由该特定基序连接的几种通路。这一基序的作用似乎也证实了其他研究活动对选定的代表性途径的深入审查。结论:虽然之前的研究提出了通路水平的转录调控机制,如通路保护环,但像本文所提出的高层次分析仍然缺失。例如,对更高水平调控基序的理解可以导致识别治疗靶点的新方法,因为它可以揭示新的和“间接”的途径来激活或沉默目标途径。然而,为了更好地揭示这种高水平的通路间调控,包括将分析扩大到其他小的非编码RNA分子,还有很多工作需要做。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A systematic analysis of a mi-RNA inter-pathway regulatory motif.

A systematic analysis of a mi-RNA inter-pathway regulatory motif.

A systematic analysis of a mi-RNA inter-pathway regulatory motif.

A systematic analysis of a mi-RNA inter-pathway regulatory motif.

Background: The continuing discovery of new types and functions of small non-coding RNAs is suggesting the presence of regulatory mechanisms far more complex than the ones currently used to study and design Gene Regulatory Networks. Just focusing on the roles of micro RNAs (miRNAs), they have been found to be part of several intra-pathway regulatory motifs. However, inter-pathway regulatory mechanisms have been often neglected and require further investigation.

Results: In this paper we present the result of a systems biology study aimed at analyzing a high-level inter-pathway regulatory motif called Pathway Protection Loop, not previously described, in which miRNAs seem to play a crucial role in the successful behavior and activation of a pathway. Through the automatic analysis of a large set of public available databases, we found statistical evidence that this inter-pathway regulatory motif is very common in several classes of KEGG Homo Sapiens pathways and concurs in creating a complex regulatory network involving several pathways connected by this specific motif. The role of this motif seems also confirmed by a deeper review of other research activities on selected representative pathways.

Conclusions: Although previous studies suggested transcriptional regulation mechanism at the pathway level such as the Pathway Protection Loop, a high-level analysis like the one proposed in this paper is still missing. The understanding of higher-level regulatory motifs could, as instance, lead to new approaches in the identification of therapeutic targets because it could unveil new and "indirect" paths to activate or silence a target pathway. However, a lot of work still needs to be done to better uncover this high-level inter-pathway regulation including enlarging the analysis to other small non-coding RNA molecules.

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