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Imprinted Genes: Genomic Conservation, Transcriptomic Dynamics and Phenomic Significance in Health and Diseases

Journal

INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES
Volume 19, Issue 10, Pages 3128-3142

Publisher

IVYSPRING INT PUBL
DOI: 10.7150/ijbs.83712

Keywords

Parent of Origin; Comparative Genomics; Gene Variation; Disease Classification

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Since its discovery, genomic imprinting has been extensively studied in terms of establishment, regulation, evolution, and function. Imprinting disturbance has been linked to various diseases. However, studies on the prevalence and relevance of imprinting have been limited by availability and resources, resulting in a gap in comparative studies. This study gathered imprinted genes from different species and identified trends and patterns in evolutionary conservation, tissue expression, and health phenomics. Imprinted genes showed distinct characteristics compared to sex differentiation genes, including less conservation, higher proportions of non-coding RNA, and preference for tissue-specific expression and limited gene pathways.
Since its discovery in 1991, genomic imprinting has been the subject of numerous studies into its mechanisms of establishment and regulation, evolution and function, and presence in multiple genomes. Disturbance of imprinting has been implicated in a range of diseases, ranging from debilitating syndromes to cancers to fetal deficiencies. Despite this, studies done on the prevalence and relevance of imprinting on genes have been limited in scope, tissue types available, and focus, by both availability and resources. This has left a gap in comparative studies. To address this, we assembled a collection of imprinted genes available in current literature covering five species. Here we sought to identify trends and motifs in the imprinted gene set (IGS) in three distinct arenas: evolutionary conservation, across-tissue expression, and health phenomics. Overall, we found that imprinted genes displayed less conservation and higher proportions of non-coding RNA while maintaining synteny. Maternally expressed genes (MEGs) and paternally expressed genes (PEGs) occupied distinct roles in tissue expression and biological pathway use, while imprinted genes collectively showed a broader tissue range, notable preference for tissue specific expression and limited gene pathways than comparable sex differentiation genes. Both human and murine imprinted genes showed the same clear phenotypic trends, that were distinct from those displayed by sex differentiation genes which were less involved in mental and nervous system disease. While both sets had representation across the genome, the IGS showed clearer clustering as expected, with PEGs significantly more represented than MEGs.

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