Page 19 - IBRO_RNA School_Abstract Book
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The microRNA editing spectrum of human brain in

           health and disease



           Arijit Mukhopadhyay

           University of Salford, Manchester, UK



           RNA  editing  is  a  post-transcriptional  modification,  which  can  provide  tissue-

           specific functions not encoded in DNA. Adenosine-to-inosine is the predominant
           editing  event  and,  along  with  cytosine-to-uracil  changes,  constitutes  canonical
           editing. The rest is non-canonical editing. We have analysed both canonical and
           non-canonical  editing  in  microRNA  from  the  human  brain  and  confirmed  its
           absence at the DNA level. All types of editing were enriched in brain including
           many  recurring  events,  which  indicated  functional  relevance  and  importance.
           Editing  in  microRNAs,  particularly  in  seed  can  significantly  alter  the  choice  of
           their target genes. We found an enrichment of the seed-editing events except for
           C-to-U  editing.  Further,  small  RNA  sequencing  of  brain  cancer  patients
           (Glioblastoma  multiforme)  identified  significant  miRNA  hypo-editing  which
           correlated with downregulation of ADAR2 both in metadata and qRT-PCR based
           validation.  Our  results  implicate  miRNA  non-canonical  editing  as  one  of  the

           contributing  factors  towards  transcriptomic  diversity  in  the  human  brain  –
           especially in the post-mitotic neurons, where  the limited cell division and DNA
           replication can limit its potential to create and maintain diversity.



           References: (i) Paul D, Ansari AH, Lal M, Mukhopadhyay A.  Noncoding RNA.
           2020       Jun      2;6(2):21.      doi:      10.3390/ncrna6020021.PMID:                32498345
           (ii) Paul D, Sinha AN, Ray A, Lal M, Nayak S, Sharma A, Mehani B, Mukherjee D,
           Laddha  SV,  Suri  A,  Sarkar  C,  Mukhopadhyay  A.  Sci  Rep.  2017  May
           26;7(1):2466. doi: 10.1038/s41598-017-02397-6.PMID: 28550310
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