Analysis of experience-regulated transcriptome and imprintome during critical periods of mouse visual system development reveals spatiotemporal dynamics
Author(s) -
Chi-Lin Hsu,
ChihHsuan Chou,
Shih-Chuan Huang,
ChiaYi Lin,
Meng-Ying Lin,
Chun-Che Tung,
Chun-Yen Lin,
Ivan Pochou Lai,
YanFang Zou,
Neil A. Youngson,
ShauPing Lin,
ChangHao Yang,
ShihKuo Chen,
Susan ShurFen Gau,
HsienSung Huang
Publication year - 2018
Publication title -
human molecular genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.811
H-Index - 276
eISSN - 1460-2083
pISSN - 0964-6906
DOI - 10.1093/hmg/ddy023
Subject(s) - biology , genomic imprinting , epigenetics , transcriptome , microrna , imprinting (psychology) , epigenesis , genetics , regulation of gene expression , gene , gene expression , dna methylation , computational biology
Visual system development is light-experience dependent, which strongly implicates epigenetic mechanisms in light-regulated maturation. Among many epigenetic processes, genomic imprinting is an epigenetic mechanism through which monoallelic gene expression occurs in a parent-of-origin-specific manner. It is unknown if genomic imprinting contributes to visual system development. We profiled the transcriptome and imprintome during critical periods of mouse visual system development under normal- and dark-rearing conditions using B6/CAST F1 hybrid mice. We identified experience-regulated, isoform-specific and brain-region-specific imprinted genes. We also found imprinted microRNAs were predominantly clustered into the Dlk1-Dio3 imprinted locus with light experience affecting some imprinted miRNA expression. Our findings provide the first comprehensive analysis of light-experience regulation of the transcriptome and imprintome during critical periods of visual system development. Our results may contribute to therapeutic strategies for visual impairments and circadian rhythm disorders resulting from a dysfunctional imprintome.
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