» Articles » PMID: 39333906

Modelling Cell Type-specific LncRNA Regulatory Network in Autism with Cycle

Overview
Publisher Biomed Central
Specialty Biology
Date 2024 Sep 28
PMID 39333906
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Autism spectrum disorder (ASD) is a class of complex neurodevelopment disorders with high genetic heterogeneity. Long non-coding RNAs (lncRNAs) are vital regulators that perform specific functions within diverse cell types and play pivotal roles in neurological diseases including ASD. Therefore, exploring lncRNA regulation would contribute to deciphering ASD molecular mechanisms. Existing computational methods utilize bulk transcriptomics data to identify lncRNA regulation in all of samples, which could reveal the commonalities of lncRNA regulation in ASD, but ignore the specificity of lncRNA regulation across various cell types.

Results: Here, we present Cycle (Cell type-specific lncRNA regulatory network) to construct the landscape of cell type-specific lncRNA regulation in ASD. We have found that each ASD cell type is unique in lncRNA regulation, and more than one-third and all cell type-specific lncRNA regulatory networks are characterized as scale-free and small-world, respectively. Across 17 ASD cell types, we have discovered 19 rewired and 11 stable modules, along with eight rewired and three stable hubs within the constructed cell type-specific lncRNA regulatory networks. Enrichment analysis reveals that the discovered rewired and stable modules and hubs are closely related to ASD. Furthermore, more similar ASD cell types tend to be connected with higher strength in the constructed cell similarity network. Finally, the comparison results demonstrate that Cycle is a potential method for uncovering cell type-specific lncRNA regulation.

Conclusion: Overall, these results illustrate that Cycle is a promising method to model the landscape of cell type-specific lncRNA regulation, and provides insights into understanding the heterogeneity of lncRNA regulation between various ASD cell types.

References
1.
Chang Q, Yang H, Wang M, Wei H, Hu F . Role of Microtubule-Associated Protein in Autism Spectrum Disorder. Neurosci Bull. 2018; 34(6):1119-1126. PMC: 6246838. DOI: 10.1007/s12264-018-0246-2. View

2.
Peng W, Koirala P, Mo Y . LncRNA-mediated regulation of cell signaling in cancer. Oncogene. 2017; 36(41):5661-5667. PMC: 6450570. DOI: 10.1038/onc.2017.184. View

3.
Salmena L, Poliseno L, Tay Y, Kats L, Pandolfi P . A ceRNA hypothesis: the Rosetta Stone of a hidden RNA language?. Cell. 2011; 146(3):353-8. PMC: 3235919. DOI: 10.1016/j.cell.2011.07.014. View

4.
Pourtavakoli A, Ghafouri-Fard S . Calcium signaling in neurodevelopment and pathophysiology of autism spectrum disorders. Mol Biol Rep. 2022; 49(11):10811-10823. DOI: 10.1007/s11033-022-07775-6. View

5.
Sacai H, Sakoori K, Konno K, Nagahama K, Suzuki H, Watanabe T . Autism spectrum disorder-like behavior caused by reduced excitatory synaptic transmission in pyramidal neurons of mouse prefrontal cortex. Nat Commun. 2020; 11(1):5140. PMC: 7552417. DOI: 10.1038/s41467-020-18861-3. View