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Integrating multiomics longitudinal data to reconstruct networks underlying lung development
Author(s) -
Jun Ding,
Farida Ahangari,
Celia R. Espinoza,
Divya Chhabra,
Teodora Nicola,
Xiting Yan,
Charitharth Vivek Lal,
James S. Hagood,
Naftali Kaminski,
Ziv BarJoseph,
Namasivayam Ambalavanan
Publication year - 2019
Publication title -
ajp lung cellular and molecular physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.892
H-Index - 163
eISSN - 1522-1504
pISSN - 1040-0605
DOI - 10.1152/ajplung.00554.2018
Subject(s) - laser capture microdissection , computational biology , epigenetics , microrna , biology , identification (biology) , systems biology , lung , gene expression , gene , genetics , medicine , botany
A comprehensive understanding of the dynamic regulatory networks that govern postnatal alveolar lung development is still lacking. To construct such a model, we profiled mRNA, microRNA, DNA methylation, and proteomics of developing murine alveoli isolated by laser capture microdissection at 14 predetermined time points. We developed a detailed comprehensive and interactive model that provides information about the major expression trajectories, the regulators of specific key events, and the impact of epigenetic changes. Intersecting the model with single-cell RNA-Seq data led to the identification of active pathways in multiple or individual cell types. We then constructed a similar model for human lung development by profiling time-series human omics data sets. Several key pathways and regulators are shared between the reconstructed models. We experimentally validated the activity of a number of predicted regulators, leading to new insights about the regulation of innate immunity during lung development.

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