Differential expression of microRNAs associated with neurodegenerative diseases and diabetic nephropathy in protein l‐isoaspartyl methyltransferase‐deficient mice. (5th August 2021)

• Record Type: Journal Article
• Authors: Su, Zhonghao; Ren, Na; Ling, Zicheng; Sheng, Lanyue; Zhou, Sirui; Guo, Chunxia; Ke, Zunji; Xu, Tiefeng; Qin, Zhenxia
• Is Part Of: Cell biology international. Volume 45:Number 11(2021)
• Page Start: 2316
• Page End: 2330
• Publication Date: 2021-08-05
• Subjects: brain -- diabetic nephropathy -- kidney -- microRNAs -- neurodegenerative diseases -- protein l‐isoaspartyl methyltransferase -- serum‐derived exosomes; Cytology -- Periodicals; Cells -- Periodicals; 571.605
• DOI: 10.1002/cbin.11679
• Languages: English
• ISSNs: 1065-6995

Abstract

Abstract: Protein l ‐isoaspartyl methyltransferase (PIMT/PCMT1), an enzyme repairing isoaspartate residues in peptides and proteins that result from the spontaneous decomposition of normal l ‐aspartyl and l ‐asparaginyl residues during aging, has been revealed to be involved in neurodegenerative diseases (NDDs) and diabetes. However, the molecular mechanisms for a putative association of PIMT dysfunction with these diseases have not been clarified. Our study aimed to identify differentially expressed microRNAs (miRNAs) in the brain and kidneys of PIMT‐deficient mice and uncover the epigenetic mechanism of PIMT‐involved NDDs and diabetic nephropathy (DN). Differentially expressed miRNAs by sequencing underwent target prediction and enrichment analysis in the brain and kidney of PIMT knockout (KO) mice and age‐matched wild‐type (WT) littermates. Sequence analysis revealed 40 differentially expressed miRNAs in the PIMT KO mouse brain including 25 upregulated miRNAs and 15 downregulated miRNAs. In the PIMT KO mouse kidney, there were 80 differentially expressed miRNAs including 40 upregulated miRNAs and 40 downregulated miRNAs. Enrichment analysis and a systematic literature review of differentially expressed miRNAs indicated the involvement of PIMT deficiency in the pathogenesis in NDDs and DN. Some overlapped differentially expressed miRNAs between the brain and kidney were quantitatively assessed in the brain, kidney, and serum‐derived exosomes, respectively. Despite being preliminary, these results may aid in investigating the pathological hallmarks and identify the potential therapeutic targets and biomarkers for PIMT dysfunction‐related NDDs and DN.