Comparison of transcriptome-wide N6-methyladenosine profiles from healthy trio families reveals regulator-mediated methylation alterations

Author:

Li Yini123ORCID,Liu Hang23,He Chuan4567ORCID,Ma Lijia23ORCID

Affiliation:

1. School of Life Sciences, Fudan University , 220 Handan Road , Shanghai 201100, China

2. Westlake Laboratory of Life Sciences and Biomedicine, Westlake University , 18 Shilongshan Road , Hangzhou 310024, Zhejiang, China

3. School of Life Sciences, Westlake University , 600 Dunyu Road , Hangzhou 310024, Zhejiang, China

4. Department of Chemistry and Institute for Biophysical Dynamics, The University of Chicago , Chicago, IL 60637 , USA

5. Howard Hughes Medical Institute, The University of Chicago , Chicago, IL 60637 , USA

6. Medical Scientist Training Program/Committee on Cancer Biology, The University of Chicago , Chicago, IL 60637 , USA

7. Department of Biochemistry and Molecular Biology, The University of Chicago , Chicago, IL 60637 , USA

Abstract

Abstract The N6-methyladenosine (m6A) modification is a highly conserved RNA modification found in eukaryotic messenger RNAs (mRNAs). It plays a vital role in regulating various biological processes. Dysregulation of m6A modifications has been linked to a range of complex genetic diseases in humans. However, there has been a lack of comprehensive characterization and comparison of m6A modifications at the transcriptome-wide level within families. To address this gap, we profiled transcriptome-wide m6A methylation in 18 individuals across 6 Yoruba trio families. The m6A methylomes of these 18 individuals revealed that m6A modifications in children showed greater similarity to each other than to their parents. This suggests that m6A modifications are influenced by multiple factors rather than solely determined by genetic factors. Additionally, we found that mRNAs exhibiting m6A modifications specific to children were enriched in cell cycle control processes, while those with m6A modifications specific to parents were associated with chromatin modifications. Furthermore, our analysis on the interactions between differentially expressed m6A-related regulatory genes and age-related genes suggested that age might be one of the factors influencing m6A modifications. In summary, our study provided a valuable dataset that highlighted the differences and functional diversity of m6A modifications within and between trio families.

Funder

Westlake Education Foundation

Basic Research Foundation of Zhejiang Province

Publisher

Oxford University Press (OUP)

Subject

Genetics

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